LKT Labs 是一家專注于防癌抗癌特殊化學品研究和開發(fā)的公司。主要提供：癌癥藥物、藥物發(fā)現(xiàn)試劑盒、天然產(chǎn)物、廣泛的生命科學研究試劑、定制合成。
美國LKT Labs 是1988年在美國成立的，為全球提供先端的藥物研發(fā)試劑、試劑盒、委托合成，并為藥物生產(chǎn)企業(yè)提供原料，最近幾年在農(nóng)藥、水產(chǎn)養(yǎng)殖業(yè)有很大程度的開發(fā)。在LKT Labs 可以找到在其他地方找不到的產(chǎn)品。

LKT Labs Q8134 Quinapril Hydrochloride

LKT Labs Q8134 Quinapril Hydrochloride

LKT 代理

LKT 代理

Proper shipping name: Toxic solid, organic, n.o.s. (Eprinomectin)"

LKT E6781 (±)-Equol 10 mg 121.9 Isoflavone, phytoestrogen found in soy; ER agonist. (R,S)-Equol; 3,4-Dihydro-3,(4-hydroxyphenyl)-2H-1-benzopyran-7-ol; 4',7-Dihydroxyisoflavane 94105-90-5 ≥98% 242.27 C15H14O3 C1C(COC2=C1C=CC(=C2)O)C3=CC=C(C=C3)O Ambient -20°C Soluble in DMSO, ethanol, dilute aqueous base.  Insoluble in water. "Lephart ED. Protective effects of equol and their polyphenolic isomers against dermal aging: microarray/protein evidence with clinical implications and unique delivery into human skin. Pharm Biol. 2013 Nov;51(11):1393-400. PMID: 23862588.

Richardson TE, Simpkins JW. R- and S-equol have equivalent cytoprotective effects in Friedreich's ataxia. BMC Pharmacol Toxicol. 2012 Oct 22;13:12. PMID: 23088310.

Choi EJ, Kim GH. Anticancer mechanism of equol in 7,12-dimethylbenz(a)anthracene-treated animals. Int J Oncol. 2011 Sep;39(3):747-54. PMID: 21667019.

Mu?oz Y, Garrido A, Valladares L. Equol is more active than soy isoflavone itself to compete for binding to thromboxane A(2) receptor in human platelets. Thromb Res. 2009 Mar;123(5):740-4. PMID: 18786699.

Kang JS, Yoon YD, Han MH, et al. Estrogen receptor-independent inhibition of tumor necrosis factor-alpha gene expression by phytoestrogen equol is mediated by blocking nuclear factor-kappaB activation in mouse macrophages. Biochem Pharmacol. 2005 Dec 19;71(1-2):136-43. PMID: 16288994.

" Not dangerous goods.

LKT E6781 (±)-Equol 25 mg 234.5 Isoflavone, phytoestrogen found in soy; ER agonist. (R,S)-Equol; 3,4-Dihydro-3,(4-hydroxyphenyl)-2H-1-benzopyran-7-ol; 4',7-Dihydroxyisoflavane 94105-90-5 ≥98% 242.27 C15H14O3 C1C(COC2=C1C=CC(=C2)O)C3=CC=C(C=C3)O Ambient -20°C Soluble in DMSO, ethanol, dilute aqueous base.  Insoluble in water. "Lephart ED. Protective effects of equol and their polyphenolic isomers against dermal aging: microarray/protein evidence with clinical implications and unique delivery into human skin. Pharm Biol. 2013 Nov;51(11):1393-400. PMID: 23862588.

Richardson TE, Simpkins JW. R- and S-equol have equivalent cytoprotective effects in Friedreich's ataxia. BMC Pharmacol Toxicol. 2012 Oct 22;13:12. PMID: 23088310.

Choi EJ, Kim GH. Anticancer mechanism of equol in 7,12-dimethylbenz(a)anthracene-treated animals. Int J Oncol. 2011 Sep;39(3):747-54. PMID: 21667019.

Mu?oz Y, Garrido A, Valladares L. Equol is more active than soy isoflavone itself to compete for binding to thromboxane A(2) receptor in human platelets. Thromb Res. 2009 Mar;123(5):740-4. PMID: 18786699.

Kang JS, Yoon YD, Han MH, et al. Estrogen receptor-independent inhibition of tumor necrosis factor-alpha gene expression by phytoestrogen equol is mediated by blocking nuclear factor-kappaB activation in mouse macrophages. Biochem Pharmacol. 2005 Dec 19;71(1-2):136-43. PMID: 16288994.

" Not dangerous goods.

LKT E6781 (±)-Equol 100 mg 609.5 Isoflavone, phytoestrogen found in soy; ER agonist. (R,S)-Equol; 3,4-Dihydro-3,(4-hydroxyphenyl)-2H-1-benzopyran-7-ol; 4',7-Dihydroxyisoflavane 94105-90-5 ≥98% 242.27 C15H14O3 C1C(COC2=C1C=CC(=C2)O)C3=CC=C(C=C3)O Ambient -20°C Soluble in DMSO, ethanol, dilute aqueous base.  Insoluble in water. "Lephart ED. Protective effects of equol and their polyphenolic isomers against dermal aging: microarray/protein evidence with clinical implications and unique delivery into human skin. Pharm Biol. 2013 Nov;51(11):1393-400. PMID: 23862588.

Richardson TE, Simpkins JW. R- and S-equol have equivalent cytoprotective effects in Friedreich's ataxia. BMC Pharmacol Toxicol. 2012 Oct 22;13:12. PMID: 23088310.

Choi EJ, Kim GH. Anticancer mechanism of equol in 7,12-dimethylbenz(a)anthracene-treated animals. Int J Oncol. 2011 Sep;39(3):747-54. PMID: 21667019.

Mu?oz Y, Garrido A, Valladares L. Equol is more active than soy isoflavone itself to compete for binding to thromboxane A(2) receptor in human platelets. Thromb Res. 2009 Mar;123(5):740-4. PMID: 18786699.

Kang JS, Yoon YD, Han MH, et al. Estrogen receptor-independent inhibition of tumor necrosis factor-alpha gene expression by phytoestrogen equol is mediated by blocking nuclear factor-kappaB activation in mouse macrophages. Biochem Pharmacol. 2005 Dec 19;71(1-2):136-43. PMID: 16288994.

" Not dangerous goods.

LKT E6814 Erdosteine 100 mg 54.4 Thiol derivative, antioxidant. [[2-Oxo-2-[(tetrahydro-2-oxo-3-thienyl)amino]ethyl]- thio]acetic acid RV-144; Secresolv 84611-23-4 ≥98% 249.31 C8H11NO4S2 C1CSC(=O)C1NC(=O)CSCC(=O)O Ambient Ambient Slightly soluble in water, methanol or ethanol. "Marabini L, Calò R, Braga PC. Protective effect of erdosteine metabolite I against hydrogen peroxide-induced oxidative DNA-damage in lung epithelial cells. Arzneimittelforschung. 2011;61(12):700-6. PMID: 22282957.

Dal Negro RW, Visconti M, Tognella S, et al. Erdosteine affects eicosanoid production in COPD. Int J Clin Pharmacol Ther. 2011 Jan;49(1):41-5. PMID: 21176724.

" Not dangerous goods.

LKT E6814 Erdosteine 500 mg 163.2 Thiol derivative, antioxidant. [[2-Oxo-2-[(tetrahydro-2-oxo-3-thienyl)amino]ethyl]- thio]acetic acid RV-144; Secresolv 84611-23-4 ≥98% 249.31 C8H11NO4S2 C1CSC(=O)C1NC(=O)CSCC(=O)O Ambient Ambient Slightly soluble in water, methanol or ethanol. "Marabini L, Calò R, Braga PC. Protective effect of erdosteine metabolite I against hydrogen peroxide-induced oxidative DNA-damage in lung epithelial cells. Arzneimittelforschung. 2011;61(12):700-6. PMID: 22282957.

Dal Negro RW, Visconti M, Tognella S, et al. Erdosteine affects eicosanoid production in COPD. Int J Clin Pharmacol Ther. 2011 Jan;49(1):41-5. PMID: 21176724.

" Not dangerous goods.

LKT E6814 Erdosteine 1 g 271.7 Thiol derivative, antioxidant. [[2-Oxo-2-[(tetrahydro-2-oxo-3-thienyl)amino]ethyl]- thio]acetic acid RV-144; Secresolv 84611-23-4 ≥98% 249.31 C8H11NO4S2 C1CSC(=O)C1NC(=O)CSCC(=O)O Ambient Ambient Slightly soluble in water, methanol or ethanol. "Marabini L, Calò R, Braga PC. Protective effect of erdosteine metabolite I against hydrogen peroxide-induced oxidative DNA-damage in lung epithelial cells. Arzneimittelforschung. 2011;61(12):700-6. PMID: 22282957.

Dal Negro RW, Visconti M, Tognella S, et al. Erdosteine affects eicosanoid production in COPD. Int J Clin Pharmacol Ther. 2011 Jan;49(1):41-5. PMID: 21176724.

" Not dangerous goods.

LKT E6825 Ergosterol 5 g 73.5 Sterol cell membrane component found in yeast and fungi. "(3β,5α)-Ergostan-3-ol

" Ergosterin, Provitamin D2. 57-87-4 ≥96% 396.65 C28H44O CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2=CC=C4C3(CCC(C4)O)C)C Protect from light and air. Ambient 4°C Practically insoluble in water. Soluble in chloroform, boiling ether, boiling alcohol. "Roberts CW, McLeod R, Rice DW, et al. Fatty acid and sterol metabolism: potential antimicrobial targets in apicomplexan and trypanosomatid parasitic protozoa. Mol Biochem Parasitol. 2003 Feb;126(2):129-42. PMID: 12615312.

Takaku T, Kimura Y, Okuda H. Isolation of an antitumor compound from Agaricus blazei Murill and its mechanism of action. J Nutr. 2001 May;131(5):1409-13. PMID: 11340091.

Yazawa Y, Yokota M, Sugiyama K. Antitumor promoting effect of an active component of Polyporus, ergosterol and related compounds on rat urinary bladder carcinogenesis in a short-term test with concanavalin A. Biol Pharm Bull. 2000 Nov;23(11):1298-302. PMID: 11085355.

" None Not dangerous goods.

LKT E6825 Ergosterol 10 g 125.9 Sterol cell membrane component found in yeast and fungi. "(3β,5α)-Ergostan-3-ol

" Ergosterin, Provitamin D2. 57-87-4 ≥96% 396.65 C28H44O CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2=CC=C4C3(CCC(C4)O)C)C Protect from light and air. Ambient 4°C Practically insoluble in water. Soluble in chloroform, boiling ether, boiling alcohol. "Roberts CW, McLeod R, Rice DW, et al. Fatty acid and sterol metabolism: potential antimicrobial targets in apicomplexan and trypanosomatid parasitic protozoa. Mol Biochem Parasitol. 2003 Feb;126(2):129-42. PMID: 12615312.

Takaku T, Kimura Y, Okuda H. Isolation of an antitumor compound from Agaricus blazei Murill and its mechanism of action. J Nutr. 2001 May;131(5):1409-13. PMID: 11340091.

Yazawa Y, Yokota M, Sugiyama K. Antitumor promoting effect of an active component of Polyporus, ergosterol and related compounds on rat urinary bladder carcinogenesis in a short-term test with concanavalin A. Biol Pharm Bull. 2000 Nov;23(11):1298-302. PMID: 11085355.

" None Not dangerous goods.

LKT E6825 Ergosterol 25 g 252.1 Sterol cell membrane component found in yeast and fungi. "(3β,5α)-Ergostan-3-ol

" Ergosterin, Provitamin D2. 57-87-4 ≥96% 396.65 C28H44O CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2=CC=C4C3(CCC(C4)O)C)C Protect from light and air. Ambient 4°C Practically insoluble in water. Soluble in chloroform, boiling ether, boiling alcohol. "Roberts CW, McLeod R, Rice DW, et al. Fatty acid and sterol metabolism: potential antimicrobial targets in apicomplexan and trypanosomatid parasitic protozoa. Mol Biochem Parasitol. 2003 Feb;126(2):129-42. PMID: 12615312.

Takaku T, Kimura Y, Okuda H. Isolation of an antitumor compound from Agaricus blazei Murill and its mechanism of action. J Nutr. 2001 May;131(5):1409-13. PMID: 11340091.

Yazawa Y, Yokota M, Sugiyama K. Antitumor promoting effect of an active component of Polyporus, ergosterol and related compounds on rat urinary bladder carcinogenesis in a short-term test with concanavalin A. Biol Pharm Bull. 2000 Nov;23(11):1298-302. PMID: 11085355.

" None Not dangerous goods.

LKT E6825 Ergosterol 100 g 829.7 Sterol cell membrane component found in yeast and fungi. "(3β,5α)-Ergostan-3-ol

" Ergosterin, Provitamin D2. 57-87-4 ≥96% 396.65 C28H44O CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2=CC=C4C3(CCC(C4)O)C)C Protect from light and air. Ambient 4°C Practically insoluble in water. Soluble in chloroform, boiling ether, boiling alcohol. "Roberts CW, McLeod R, Rice DW, et al. Fatty acid and sterol metabolism: potential antimicrobial targets in apicomplexan and trypanosomatid parasitic protozoa. Mol Biochem Parasitol. 2003 Feb;126(2):129-42. PMID: 12615312.

Takaku T, Kimura Y, Okuda H. Isolation of an antitumor compound from Agaricus blazei Murill and its mechanism of action. J Nutr. 2001 May;131(5):1409-13. PMID: 11340091.

Yazawa Y, Yokota M, Sugiyama K. Antitumor promoting effect of an active component of Polyporus, ergosterol and related compounds on rat urinary bladder carcinogenesis in a short-term test with concanavalin A. Biol Pharm Bull. 2000 Nov;23(11):1298-302. PMID: 11085355.

" None Not dangerous goods.

LKT E6846 Erlotinib Hydrochloride 10 mg 54.4 EGFR inhibitor. 183319-69-9 ≥98% 429.9 C22H23N3O4 HCl COCCOC1=C(C=C2C(=C1)C(=NC=N2)NC3=CC=CC(=C3)C#C)OCCOC.Cl Ambient Ambient DMSO (16 mg/mL) H2O "Li YY, Lam SK, Mak JC, et al. Erlotinib-induced autophagy in epidermal growth factor receptor mutated non-small cell lung cancer. Lung Cancer. 2013 Sep;81(3):354-61. PMID: 23769318.

Miyabayashi K, Ijichi H, Mohri D, et al. Erlotinib prolongs survival in pancreatic cancer by blocking gemcitabine-induced MAPK signals. Cancer Res. 2013 Apr 1;73(7):2221-34. PMID: 23378339.

Weickhardt AJ, Price TJ, Chong G, et al. Dual targeting of the epidermal growth factor receptor using the combination of cetuximab and erlotinib: preclinical evaluation and results of the phase II DUX study in chemotherapy-refractory, advanced colorectal cancer. J Clin Oncol. 2012 May 1;30(13):1505-12. PMID: 22412142.

Zerbe LK, Dwyer-Nield LD, Fritz JM, et al. Inhibition by erlotinib of primary lung adenocarcinoma at an early stage in male mice. Cancer Chemother Pharmacol. 2008 Sep;62(4):605-20. PMID: 18030469.

Ling YH, Li T, Yuan Z, et al. Erlotinib, an effective epidermal growth factor receptor tyrosine kinase inhibitor, induces p27KIP1 up-regulation and nuclear translocation in association with cell growth inhibition and G1/S phase arrest in human non-small-cell lung cancer cell lines. Mol Pharmacol. 2007 Aug;72(2):248-58. PMID: 17456787.

" Xn, Carc. Cat. 3, Repr. Cat. 3, N "UN number: 2811     Class: 6.1     Packing Group: III

Proper shipping name: Toxic solid, organic, n.o.s. (Erlotinib hydrochloride)"

LKT E6846 Erlotinib Hydrochloride 100 mg 197.1 EGFR inhibitor. 183319-69-9 ≥98% 429.9 C22H23N3O4 HCl COCCOC1=C(C=C2C(=C1)C(=NC=N2)NC3=CC=CC(=C3)C#C)OCCOC.Cl Ambient Ambient DMSO (16 mg/mL) H2O "Li YY, Lam SK, Mak JC, et al. Erlotinib-induced autophagy in epidermal growth factor receptor mutated non-small cell lung cancer. Lung Cancer. 2013 Sep;81(3):354-61. PMID: 23769318.

Miyabayashi K, Ijichi H, Mohri D, et al. Erlotinib prolongs survival in pancreatic cancer by blocking gemcitabine-induced MAPK signals. Cancer Res. 2013 Apr 1;73(7):2221-34. PMID: 23378339.

Weickhardt AJ, Price TJ, Chong G, et al. Dual targeting of the epidermal growth factor receptor using the combination of cetuximab and erlotinib: preclinical evaluation and results of the phase II DUX study in chemotherapy-refractory, advanced colorectal cancer. J Clin Oncol. 2012 May 1;30(13):1505-12. PMID: 22412142.

Zerbe LK, Dwyer-Nield LD, Fritz JM, et al. Inhibition by erlotinib of primary lung adenocarcinoma at an early stage in male mice. Cancer Chemother Pharmacol. 2008 Sep;62(4):605-20. PMID: 18030469.

Ling YH, Li T, Yuan Z, et al. Erlotinib, an effective epidermal growth factor receptor tyrosine kinase inhibitor, induces p27KIP1 up-regulation and nuclear translocation in association with cell growth inhibition and G1/S phase arrest in human non-small-cell lung cancer cell lines. Mol Pharmacol. 2007 Aug;72(2):248-58. PMID: 17456787.

" Xn, Carc. Cat. 3, Repr. Cat. 3, N "UN number: 2811     Class: 6.1     Packing Group: III

Proper shipping name: Toxic solid, organic, n.o.s. (Erlotinib hydrochloride)"

LKT E6846 Erlotinib Hydrochloride 25 mg 115.5 EGFR inhibitor. 183319-69-9 ≥98% 429.9 C22H23N3O4 HCl COCCOC1=C(C=C2C(=C1)C(=NC=N2)NC3=CC=CC(=C3)C#C)OCCOC.Cl Ambient Ambient DMSO (16 mg/mL) H2O "Li YY, Lam SK, Mak JC, et al. Erlotinib-induced autophagy in epidermal growth factor receptor mutated non-small cell lung cancer. Lung Cancer. 2013 Sep;81(3):354-61. PMID: 23769318.

Miyabayashi K, Ijichi H, Mohri D, et al. Erlotinib prolongs survival in pancreatic cancer by blocking gemcitabine-induced MAPK signals. Cancer Res. 2013 Apr 1;73(7):2221-34. PMID: 23378339.

Weickhardt AJ, Price TJ, Chong G, et al. Dual targeting of the epidermal growth factor receptor using the combination of cetuximab and erlotinib: preclinical evaluation and results of the phase II DUX study in chemotherapy-refractory, advanced colorectal cancer. J Clin Oncol. 2012 May 1;30(13):1505-12. PMID: 22412142.

Zerbe LK, Dwyer-Nield LD, Fritz JM, et al. Inhibition by erlotinib of primary lung adenocarcinoma at an early stage in male mice. Cancer Chemother Pharmacol. 2008 Sep;62(4):605-20. PMID: 18030469.

Ling YH, Li T, Yuan Z, et al. Erlotinib, an effective epidermal growth factor receptor tyrosine kinase inhibitor, induces p27KIP1 up-regulation and nuclear translocation in association with cell growth inhibition and G1/S phase arrest in human non-small-cell lung cancer cell lines. Mol Pharmacol. 2007 Aug;72(2):248-58. PMID: 17456787.

" Xn, Carc. Cat. 3, Repr. Cat. 3, N "UN number: 2811     Class: 6.1     Packing Group: III

Proper shipping name: Toxic solid, organic, n.o.s. (Erlotinib hydrochloride)"

LKT E6993 Erythromycin Resistance Peptide MRLFV 1 mg 63 Peptide, confers resistance against macrolide antibiotics by preventing antibiotic-ribosome interactions. E-peptide ≥95% 664.86 C31H52N8O6S Ambient -20°C Verdier L, Gharbi-Benarous J, Bertho G, et al.  Antibiotic resistance peptides: interaction of peptides conferring macrolide and ketolide resistance with Staphylococcus aureus ribosomes: conformation of bound peptides as determined by transferred NOE experiments. Biochemistry. 2002 Apr 2;41(13):4218-29. PMID: 11914067.

LKT E6993 Erythromycin Resistance Peptide MRLFV 2 mg 104.9 Peptide, confers resistance against macrolide antibiotics by preventing antibiotic-ribosome interactions. E-peptide ≥95% 664.86 C31H52N8O6S Ambient -20°C Verdier L, Gharbi-Benarous J, Bertho G, et al.  Antibiotic resistance peptides: interaction of peptides conferring macrolide and ketolide resistance with Staphylococcus aureus ribosomes: conformation of bound peptides as determined by transferred NOE experiments. Biochemistry. 2002 Apr 2;41(13):4218-29. PMID: 11914067.

LKT E6993 Erythromycin Resistance Peptide MRLFV 5 mg 186 Peptide, confers resistance against macrolide antibiotics by preventing antibiotic-ribosome interactions. E-peptide ≥95% 664.86 C31H52N8O6S Ambient -20°C Verdier L, Gharbi-Benarous J, Bertho G, et al.  Antibiotic resistance peptides: interaction of peptides conferring macrolide and ketolide resistance with Staphylococcus aureus ribosomes: conformation of bound peptides as determined by transferred NOE experiments. Biochemistry. 2002 Apr 2;41(13):4218-29. PMID: 11914067.

LKT E6994 Erythromycin 5 g 47.6 Macrolide; protein translation inhibitor, mammalian mRNA splicing inhibitor. "Erythromycin A

" Abomacetin; Aknin; EMU; E-Mycin; Erymax; Erycen; Erycin. 114-07-8 ≥94% 733.93 C37H67NO13 CCC1C(C(C(C(=O)C(CC(C(C(C(C(C(=O)O1)C)OC2CC(C(C(O2)C)O)(C)OC)C)OC3C(C(CC(O3)C)N(C)C)O)(C)O)C)C)O)(C)O Ambient Ambient Very slightly soluble in water (~2 mg/ml). Freely soluble in alcohols, acetone, ethyl acetate, acetonitrile or chloroform. "Hertweck M, Hiller R, Mueller MW. Inhibition of nuclear pre-mRNA splicing by antibiotics in vitro. Eur J Biochem. 2002 Jan;269(1):175-83. PMID: 11784311.

Menninger JR, Otto DP. Erythromycin, carbomycin, and spiramycin inhibit protein synthesis by stimulating the dissociation of peptidyl-tRNA from ribosomes. Antimicrob Agents Chemother. 1982 May;21(5):811-8. PMID: 6179465." None Not dangerous goods.

LKT E6994 Erythromycin 25 g 136 Macrolide; protein translation inhibitor, mammalian mRNA splicing inhibitor. "Erythromycin A

" Abomacetin; Aknin; EMU; E-Mycin; Erymax; Erycen; Erycin. 114-07-8 ≥94% 733.93 C37H67NO13 CCC1C(C(C(C(=O)C(CC(C(C(C(C(C(=O)O1)C)OC2CC(C(C(O2)C)O)(C)OC)C)OC3C(C(CC(O3)C)N(C)C)O)(C)O)C)C)O)(C)O Ambient Ambient Very slightly soluble in water (~2 mg/ml). Freely soluble in alcohols, acetone, ethyl acetate, acetonitrile or chloroform. "Hertweck M, Hiller R, Mueller MW. Inhibition of nuclear pre-mRNA splicing by antibiotics in vitro. Eur J Biochem. 2002 Jan;269(1):175-83. PMID: 11784311.

Menninger JR, Otto DP. Erythromycin, carbomycin, and spiramycin inhibit protein synthesis by stimulating the dissociation of peptidyl-tRNA from ribosomes. Antimicrob Agents Chemother. 1982 May;21(5):811-8. PMID: 6179465." None Not dangerous goods.

LKT E6994 Erythromycin 100 g 434.9 Macrolide; protein translation inhibitor, mammalian mRNA splicing inhibitor. "Erythromycin A

" Abomacetin; Aknin; EMU; E-Mycin; Erymax; Erycen; Erycin. 114-07-8 ≥94% 733.93 C37H67NO13 CCC1C(C(C(C(=O)C(CC(C(C(C(C(C(=O)O1)C)OC2CC(C(C(O2)C)O)(C)OC)C)OC3C(C(CC(O3)C)N(C)C)O)(C)O)C)C)O)(C)O Ambient Ambient Very slightly soluble in water (~2 mg/ml). Freely soluble in alcohols, acetone, ethyl acetate, acetonitrile or chloroform. "Hertweck M, Hiller R, Mueller MW. Inhibition of nuclear pre-mRNA splicing by antibiotics in vitro. Eur J Biochem. 2002 Jan;269(1):175-83. PMID: 11784311.

Menninger JR, Otto DP. Erythromycin, carbomycin, and spiramycin inhibit protein synthesis by stimulating the dissociation of peptidyl-tRNA from ribosomes. Antimicrob Agents Chemother. 1982 May;21(5):811-8. PMID: 6179465." None Not dangerous goods.

LKT E6995 Erythromycin Ethylsuccinate 5 g 47.6 Macrolide; protein translation inhibitor, mammalian mRNA splicing inhibitor. Anamycin E.E.S.; Arpimycin; Durapaediat; E-Mycin E; Eryliquid; Eryped. 41342-53-4 ≥97% 862.05 C43H75NO16 CCC1C(C(C(C(=O)C(CC(C(C(C(C(C(=O)O1)C)OC2CC(C(C(O2)C)O)(C)OC)C)OC3C(C(CC(O3)C)N(C)C)OC(=O)CCC(=O)OCC)(C)O)C)C)O)(C)O Ambient Ambient Very slightly soluble in water. Soluble in acetone (500 mg/L), methanol (250 mg/mL), or ethanol (110 mg/mL). "Hertweck M, Hiller R, Mueller MW. Inhibition of nuclear pre-mRNA splicing by antibiotics in vitro. Eur J Biochem. 2002 Jan;269(1):175-83. PMID: 11784311.

Menninger JR, Otto DP. Erythromycin, carbomycin, and spiramycin inhibit protein synthesis by stimulating the dissociation of peptidyl-tRNA from ribosomes. Antimicrob Agents Chemother. 1982 May;21(5):811-8. PMID: 6179465." Xi Not dangerous goods.

LKT E6995 Erythromycin Ethylsuccinate 25 g 136 Macrolide; protein translation inhibitor, mammalian mRNA splicing inhibitor. Anamycin E.E.S.; Arpimycin; Durapaediat; E-Mycin E; Eryliquid; Eryped. 41342-53-4 ≥97% 862.05 C43H75NO16 CCC1C(C(C(C(=O)C(CC(C(C(C(C(C(=O)O1)C)OC2CC(C(C(O2)C)O)(C)OC)C)OC3C(C(CC(O3)C)N(C)C)OC(=O)CCC(=O)OCC)(C)O)C)C)O)(C)O Ambient Ambient Very slightly soluble in water. Soluble in acetone (500 mg/L), methanol (250 mg/mL), or ethanol (110 mg/mL). "Hertweck M, Hiller R, Mueller MW. Inhibition of nuclear pre-mRNA splicing by antibiotics in vitro. Eur J Biochem. 2002 Jan;269(1):175-83. PMID: 11784311.

Menninger JR, Otto DP. Erythromycin, carbomycin, and spiramycin inhibit protein synthesis by stimulating the dissociation of peptidyl-tRNA from ribosomes. Antimicrob Agents Chemother. 1982 May;21(5):811-8. PMID: 6179465." Xi Not dangerous goods.

LKT E6995 Erythromycin Ethylsuccinate 100 g 434.9 Macrolide; protein translation inhibitor, mammalian mRNA splicing inhibitor. Anamycin E.E.S.; Arpimycin; Durapaediat; E-Mycin E; Eryliquid; Eryped. 41342-53-4 ≥97% 862.05 C43H75NO16 CCC1C(C(C(C(=O)C(CC(C(C(C(C(C(=O)O1)C)OC2CC(C(C(O2)C)O)(C)OC)C)OC3C(C(CC(O3)C)N(C)C)OC(=O)CCC(=O)OCC)(C)O)C)C)O)(C)O Ambient Ambient Very slightly soluble in water. Soluble in acetone (500 mg/L), methanol (250 mg/mL), or ethanol (110 mg/mL). "Hertweck M, Hiller R, Mueller MW. Inhibition of nuclear pre-mRNA splicing by antibiotics in vitro. Eur J Biochem. 2002 Jan;269(1):175-83. PMID: 11784311.

Menninger JR, Otto DP. Erythromycin, carbomycin, and spiramycin inhibit protein synthesis by stimulating the dissociation of peptidyl-tRNA from ribosomes. Antimicrob Agents Chemother. 1982 May;21(5):811-8. PMID: 6179465." Xi Not dangerous goods.

LKT E6996 Erythromycin Thiocyanate 25 g 150.4 Macrolide; protein translation inhibitor, mammalian mRNA splicing inhibitor. 7704-67-8 ≥90% 793.02 C37H67NO13 HSCN CCC1C(C(C(C(=O)C(CC(C(C(C(C(C(=O)O1)C)OC2CC(C(C(O2)C)O)(C)OC)C)OC3C(C(CC(O3)C)N(C)C)O)(C)O)C)C)O)(C)O.C(#N)S Ambient Ambient Soluble in alcohol. "Hertweck M, Hiller R, Mueller MW. Inhibition of nuclear pre-mRNA splicing by antibiotics in vitro. Eur J Biochem. 2002 Jan;269(1):175-83. PMID: 11784311.

Menninger JR, Otto DP. Erythromycin, carbomycin, and spiramycin inhibit protein synthesis by stimulating the dissociation of peptidyl-tRNA from ribosomes. Antimicrob Agents Chemother. 1982 May;21(5):811-8. PMID: 6179465." Not dangerous goods.

LKT E6996 Erythromycin Thiocyanate 100 g 461.1 Macrolide; protein translation inhibitor, mammalian mRNA splicing inhibitor. 7704-67-8 ≥90% 793.02 C37H67NO13 HSCN CCC1C(C(C(C(=O)C(CC(C(C(C(C(C(=O)O1)C)OC2CC(C(C(O2)C)O)(C)OC)C)OC3C(C(CC(O3)C)N(C)C)O)(C)O)C)C)O)(C)O.C(#N)S Ambient Ambient Soluble in alcohol. "Hertweck M, Hiller R, Mueller MW. Inhibition of nuclear pre-mRNA splicing by antibiotics in vitro. Eur J Biochem. 2002 Jan;269(1):175-83. PMID: 11784311.

Menninger JR, Otto DP. Erythromycin, carbomycin, and spiramycin inhibit protein synthesis by stimulating the dissociation of peptidyl-tRNA from ribosomes. Antimicrob Agents Chemother. 1982 May;21(5):811-8. PMID: 6179465." Not dangerous goods.

LKT E6997 Erythropoietin 50 U 963.7 Endogenous glycoprotein hormone involved in red blood cell production; EpoR agonist. Erythropoiesis stimulating factor; Hemopoietine; ESF; Epo 11096-26-7 ≥97% Dry Ice -80°C Soluble in water. "Liu S, Ren J, Hong Z, et al. Efficacy of erythropoietin combined with enteral nutrition for the treatment of anemia in Crohn's disease: a prospective cohort study. Nutr Clin Pract. 2013 Feb;28(1):120-7. PMID: 23064018.

Ashby DR, Gale DP, Busbridge M, et al. Erythropoietin administration in humans causes a marked and prolonged reduction in circulating hepcidin. Haematologica. 2010 Mar;95(3):505-8. PMID: 19833632.

Miskowiak K, Inkster B, Selvaraj S, et al. Erythropoietin improves mood and modulates the cognitive and neural processing of emotion 3 days post administration. Neuropsychopharmacology. 2008 Feb;33(3):611-8. PMID: 17473836.

" Xi Not dangerous goods.

LKT E7228 Ethacridine Lactate Monohydrate 25 g 67.9 Aromatic acridine derivative, DNA intercalator. 7-Ethoxy-3,9-acridinediamine lactate monohydrate Acrino; Rimaon; Rivano; Vucine; Acrolactine; Ethodin; Metifex 6402-23-9 ≥98% 361.39 C15H15N3O C3H6O3 H2O CCOC1=CC2=C(C3=C(C=C(C=C3)N)N=C2C=C1)N.CC(C(=O)O)O.O Ambient Ambient Partially soluble in 15 parts water. Soluble in 9 parts boiling water. "Mei Q, Li X, Liu H, et al. Effectiveness of mifepristone in combination with ethacridine lactate for second trimester pregnancy termination. Eur J Obstet Gynecol Reprod Biol. 2014 Jul;178:12-5. PMID: 24948048.

Oie S, Kamiya A. Microbial contamination of antiseptic-soaked cotton balls. Biol Pharm Bull. 1997 Jun;20(6):667-9. PMID: 9212987.

Tien KH. Intraamniotic injection of ethacridine for second-trimester induction of labor. Obstet Gynecol. 1983 Jun;61(6):733-6. PMID: 6843933.

" Xi Not dangerous goods.

LKT E7228 Ethacridine Lactate Monohydrate 50 g 122.3 Aromatic acridine derivative, DNA intercalator. 7-Ethoxy-3,9-acridinediamine lactate monohydrate Acrino; Rimaon; Rivano; Vucine; Acrolactine; Ethodin; Metifex 6402-23-9 ≥98% 361.39 C15H15N3O C3H6O3 H2O CCOC1=CC2=C(C3=C(C=C(C=C3)N)N=C2C=C1)N.CC(C(=O)O)O.O Ambient Ambient Partially soluble in 15 parts water. Soluble in 9 parts boiling water. "Mei Q, Li X, Liu H, et al. Effectiveness of mifepristone in combination with ethacridine lactate for second trimester pregnancy termination. Eur J Obstet Gynecol Reprod Biol. 2014 Jul;178:12-5. PMID: 24948048.

Oie S, Kamiya A. Microbial contamination of antiseptic-soaked cotton balls. Biol Pharm Bull. 1997 Jun;20(6):667-9. PMID: 9212987.

Tien KH. Intraamniotic injection of ethacridine for second-trimester induction of labor. Obstet Gynecol. 1983 Jun;61(6):733-6. PMID: 6843933.

" Xi Not dangerous goods.

LKT E7228 Ethacridine Lactate Monohydrate 100 g 237.8 Aromatic acridine derivative, DNA intercalator. 7-Ethoxy-3,9-acridinediamine lactate monohydrate Acrino; Rimaon; Rivano; Vucine; Acrolactine; Ethodin; Metifex 6402-23-9 ≥98% 361.39 C15H15N3O C3H6O3 H2O CCOC1=CC2=C(C3=C(C=C(C=C3)N)N=C2C=C1)N.CC(C(=O)O)O.O Ambient Ambient Partially soluble in 15 parts water. Soluble in 9 parts boiling water. "Mei Q, Li X, Liu H, et al. Effectiveness of mifepristone in combination with ethacridine lactate for second trimester pregnancy termination. Eur J Obstet Gynecol Reprod Biol. 2014 Jul;178:12-5. PMID: 24948048.

Oie S, Kamiya A. Microbial contamination of antiseptic-soaked cotton balls. Biol Pharm Bull. 1997 Jun;20(6):667-9. PMID: 9212987.

Tien KH. Intraamniotic injection of ethacridine for second-trimester induction of labor. Obstet Gynecol. 1983 Jun;61(6):733-6. PMID: 6843933.

" Xi Not dangerous goods.

LKT E7230 Ethambutol Dihydrochloride 25 g 99.8 Arabinosyl transferase inhibitor. 2,2'-(1,2-Ethanediyldiimino)bis-1-butanol (+)-2,2'-(ethylenediimino)di-1-butanol; EMB 1070-11-7 ≥98% 277.24 C10H24N2O2 CCC(CO)NCCNC(CC)CO.Cl.Cl Ambient Ambient Soluble in water. Sparingly soluble in ethanol. "Plinke C, Walter K, Aly S, et al. Mycobacterium tuberculosis embB codon 306 mutations confer moderately increased resistance to ethambutol in vitro and in vivo. Antimicrob Agents Chemother. 2011 Jun;55(6):2891-6. PMID: 21444710.

Kahana LM. Ethambutol in tuberculosis. Biomed Pharmacother. 1990;44(1):21-3. PMID: 1369688.

" T Not dangerous goods.

LKT E7230 Ethambutol Dihydrochloride 100 g 330.8 Arabinosyl transferase inhibitor. 2,2'-(1,2-Ethanediyldiimino)bis-1-butanol (+)-2,2'-(ethylenediimino)di-1-butanol; EMB 1070-11-7 ≥98% 277.24 C10H24N2O2 CCC(CO)NCCNC(CC)CO.Cl.Cl Ambient Ambient Soluble in water. Sparingly soluble in ethanol. "Plinke C, Walter K, Aly S, et al. Mycobacterium tuberculosis embB codon 306 mutations confer moderately increased resistance to ethambutol in vitro and in vivo. Antimicrob Agents Chemother. 2011 Jun;55(6):2891-6. PMID: 21444710.

Kahana LM. Ethambutol in tuberculosis. Biomed Pharmacother. 1990;44(1):21-3. PMID: 1369688.

" T Not dangerous goods.

LKT E7309 Esculetin 500 mg 50.3 Coumarin lactone found in chicory and other plant sources; β-catenin inhibitor. 6,7-Dihydroxy-2H-1-benzopyran-2-one 6,7-Dihydroxycoumarin; Cichorigenin 305-01-1 ≥98% 178.14 C9H6O4 C1=CC(=O)OC2=CC(=C(C=C21)O)O Ambient Ambient Soluble in dil alkalies, hot alcohol or glacial acetic acid. Insoluble in ether or boiling water. "Kim Y, Park Y, Namkoong S, et al. Esculetin inhibits the inflammatory response by inducing heme oxygenase-1 in cocultured macrophages and adipocytes. Food Funct. 2014 Aug 20;5(9):2371-7. PMID: 25088305.

Rubio V, Calvi?o E, García-Pérez A, et al. Human acute promyelocytic leukemia NB4 cells are sensitive to esculetin through induction of an apoptotic mechanism. Chem Biol Interact. 2014 Jul 1;220C:129-139. PMID: 24995577.

Medina ME, Galano A, Alvarez-Idaboy JR. Theoretical study on the peroxyl radicals scavenging activity of esculetin and its regeneration in aqueous solution. Phys Chem Chem Phys. 2014 Jan 21;16(3):1197-207. PMID: 24292723.

Lee SY, Lim TG, Chen H, et al. Esculetin suppresses proliferation of human colon cancer cells by directly targeting β-catenin. Cancer Prev Res (Phila). 2013 Dec;6(12):1356-64. PMID: 24104353.

Karmase A, Birari R, Bhutani KK. Evaluation of anti-obesity effect of Aegle marmelos leaves. Phytomedicine. 2013 Jul 15;20(10):805-12. PMID: 23632084.

Subramaniam SR, Ellis EM. Neuroprotective effects of umbelliferone and esculetin in a mouse model of Parkinson's disease. J Neurosci Res. 2013 Mar;91(3):453-61. PMID: 23184853.

" Xi Not dangerous goods.

LKT E7309 Esculetin 1 g 84.9 Coumarin lactone found in chicory and other plant sources; β-catenin inhibitor. 6,7-Dihydroxy-2H-1-benzopyran-2-one 6,7-Dihydroxycoumarin; Cichorigenin 305-01-1 ≥98% 178.14 C9H6O4 C1=CC(=O)OC2=CC(=C(C=C21)O)O Ambient Ambient Soluble in dil alkalies, hot alcohol or glacial acetic acid. Insoluble in ether or boiling water. "Kim Y, Park Y, Namkoong S, et al. Esculetin inhibits the inflammatory response by inducing heme oxygenase-1 in cocultured macrophages and adipocytes. Food Funct. 2014 Aug 20;5(9):2371-7. PMID: 25088305.

Rubio V, Calvi?o E, García-Pérez A, et al. Human acute promyelocytic leukemia NB4 cells are sensitive to esculetin through induction of an apoptotic mechanism. Chem Biol Interact. 2014 Jul 1;220C:129-139. PMID: 24995577.

Medina ME, Galano A, Alvarez-Idaboy JR. Theoretical study on the peroxyl radicals scavenging activity of esculetin and its regeneration in aqueous solution. Phys Chem Chem Phys. 2014 Jan 21;16(3):1197-207. PMID: 24292723.

Lee SY, Lim TG, Chen H, et al. Esculetin suppresses proliferation of human colon cancer cells by directly targeting β-catenin. Cancer Prev Res (Phila). 2013 Dec;6(12):1356-64. PMID: 24104353.

Karmase A, Birari R, Bhutani KK. Evaluation of anti-obesity effect of Aegle marmelos leaves. Phytomedicine. 2013 Jul 15;20(10):805-12. PMID: 23632084.

Subramaniam SR, Ellis EM. Neuroprotective effects of umbelliferone and esculetin in a mouse model of Parkinson's disease. J Neurosci Res. 2013 Mar;91(3):453-61. PMID: 23184853.

" Xi Not dangerous goods.

LKT E7310 Esculin 5 g 70.4 Coumarin glucoside found in Aesculus, Daphne, and Bursaria. 6-(β-D-Glucopyranosyloxy)-7-hydroxy-2H-1- benzopyran-2-one Esculin hydrate; Esculoside; Bicolorin; Enallachrome; Polychrome; Escosyl 531-75-9 ≥97% 340.28 C15H16O9 C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O Ambient Ambient Slightly soluble in water. Soluble in methanol "Kang KS, Lee W, Jung Y, et al. Protective effect of esculin on streptozotocin-induced diabetic renal damage in mice. J Agric Food Chem. 2014 Mar 5;62(9):2069-76. PMID: 24484395.

Naaz F, Abdin MZ, Javed S. Protective effect of esculin against prooxidant aflatoxin B1-induced nephrotoxicity in mice. Mycotoxin Res. 2014 Feb;30(1):25-32. PMID: 24326591.

Raemy A, Meylan M, Casati S, et al. Phenotypic and genotypic identification of streptococci and related bacteria isolated from bovine intramammary infections. Acta Vet Scand. 2013 Jul 18;55:53. PMID: 23866930.

" None Not dangerous goods.

LKT E7310 Esculin 10 g 111.7 Coumarin glucoside found in Aesculus, Daphne, and Bursaria. 6-(β-D-Glucopyranosyloxy)-7-hydroxy-2H-1- benzopyran-2-one Esculin hydrate; Esculoside; Bicolorin; Enallachrome; Polychrome; Escosyl 531-75-9 ≥97% 340.28 C15H16O9 C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O Ambient Ambient Slightly soluble in water. Soluble in methanol "Kang KS, Lee W, Jung Y, et al. Protective effect of esculin on streptozotocin-induced diabetic renal damage in mice. J Agric Food Chem. 2014 Mar 5;62(9):2069-76. PMID: 24484395.

Naaz F, Abdin MZ, Javed S. Protective effect of esculin against prooxidant aflatoxin B1-induced nephrotoxicity in mice. Mycotoxin Res. 2014 Feb;30(1):25-32. PMID: 24326591.

Raemy A, Meylan M, Casati S, et al. Phenotypic and genotypic identification of streptococci and related bacteria isolated from bovine intramammary infections. Acta Vet Scand. 2013 Jul 18;55:53. PMID: 23866930.

" None Not dangerous goods.

LKT E7324 Ethisterone 1 g 33.9 Synthetic steroid hormone, contraceptive; PR agonist. 17α-Hydroxypregn-4-en-20-yn-3-one Lutocyclin; Ora-Lutin; Progestoral; Trosinone 434-03-7 ≥98% 312.45 C21H28O2 CC12CCC(=O)C=C1CCC3C2CCC4(C3CCC4(C#C)O)C Ambient Ambient Slightly soluble in alcohol, acetone, ether, and chloroform. Practically insoluble in water. "Levine PM, Imberg K, Garabedian MJ, et al. M*lent peptidomimetic conjugates: a versatile platform for modulating androgen receptor activity. J Am Chem Soc. 2012 Apr 25;134(16):6912-5. PMID: 22509763.

Forinash AB, Evans SL. New hormonal contraceptives: a comprehensive review of the literature. Pharmacotherapy. 2003 Dec;23(12):1573-91. PMID: 14695038.

" T Not dangerous goods.

LKT E7324 Ethisterone 5 g 67.9 Synthetic steroid hormone, contraceptive; PR agonist. 17α-Hydroxypregn-4-en-20-yn-3-one Lutocyclin; Ora-Lutin; Progestoral; Trosinone 434-03-7 ≥98% 312.45 C21H28O2 CC12CCC(=O)C=C1CCC3C2CCC4(C3CCC4(C#C)O)C Ambient Ambient Slightly soluble in alcohol, acetone, ether, and chloroform. Practically insoluble in water. "Levine PM, Imberg K, Garabedian MJ, et al. M*lent peptidomimetic conjugates: a versatile platform for modulating androgen receptor activity. J Am Chem Soc. 2012 Apr 25;134(16):6912-5. PMID: 22509763.

Forinash AB, Evans SL. New hormonal contraceptives: a comprehensive review of the literature. Pharmacotherapy. 2003 Dec;23(12):1573-91. PMID: 14695038.

" T Not dangerous goods.

LKT E7324 Ethisterone 25 g 212.3 Synthetic steroid hormone, contraceptive; PR agonist. 17α-Hydroxypregn-4-en-20-yn-3-one Lutocyclin; Ora-Lutin; Progestoral; Trosinone 434-03-7 ≥98% 312.45 C21H28O2 CC12CCC(=O)C=C1CCC3C2CCC4(C3CCC4(C#C)O)C Ambient Ambient Slightly soluble in alcohol, acetone, ether, and chloroform. Practically insoluble in water. "Levine PM, Imberg K, Garabedian MJ, et al. M*lent peptidomimetic conjugates: a versatile platform for modulating androgen receptor activity. J Am Chem Soc. 2012 Apr 25;134(16):6912-5. PMID: 22509763.

Forinash AB, Evans SL. New hormonal contraceptives: a comprehensive review of the literature. Pharmacotherapy. 2003 Dec;23(12):1573-91. PMID: 14695038.

" T Not dangerous goods.

LKT E7324 Ethisterone 100 g 679.5 Synthetic steroid hormone, contraceptive; PR agonist. 17α-Hydroxypregn-4-en-20-yn-3-one Lutocyclin; Ora-Lutin; Progestoral; Trosinone 434-03-7 ≥98% 312.45 C21H28O2 CC12CCC(=O)C=C1CCC3C2CCC4(C3CCC4(C#C)O)C Ambient Ambient Slightly soluble in alcohol, acetone, ether, and chloroform. Practically insoluble in water. "Levine PM, Imberg K, Garabedian MJ, et al. M*lent peptidomimetic conjugates: a versatile platform for modulating androgen receptor activity. J Am Chem Soc. 2012 Apr 25;134(16):6912-5. PMID: 22509763.

Forinash AB, Evans SL. New hormonal contraceptives: a comprehensive review of the literature. Pharmacotherapy. 2003 Dec;23(12):1573-91. PMID: 14695038.

" T Not dangerous goods.

LKT E7329 Ethoxyquin 100 g 80.4 Quinoline, food preservative; HSP90 inhibitor. 6-Ethoxy-1,2-dihydro-2,2,4-trimethylquinoline EMQ; Santoflex; Santoquin 91-53-2 ≥75% 217.31 C14H19NO CCOC1=CC2=C(C=C1)NC(C=C2C)(C)C Ambient 4°C Soluble in ethanol. "Sadikot T, Swink M, Eskew JD, et al. Development of a high-throughput screening cancer cell-based luciferase refolding assay for identifying Hsp90 inhibitors. Assay Drug Dev Technol. 2013 Oct;11(8):478-88. PMID: 24127661.

?rnsrud R, Arukwe A, Bohne V, et al. Investigations on the metabolism and potentially adverse effects of ethoxyquin dimer, a major metabolite of the synthetic antioxidant ethoxyquin in salmon muscle. J Food Prot. 2011 Sep;74(9):1574-80. PMID: 21902931.

Kumar S, Engman L, Valgimigli L, et al. Antioxidant profile of ethoxyquin and some of its S, Se, and Te analogues. J Org Chem. 2007 Aug 3;72(16):6046-55. PMID: 17602530.

" Xn Not dangerous goods.

LKT E7329 Ethoxyquin 250 g 174.7 Quinoline, food preservative; HSP90 inhibitor. 6-Ethoxy-1,2-dihydro-2,2,4-trimethylquinoline EMQ; Santoflex; Santoquin 91-53-2 ≥75% 217.31 C14H19NO CCOC1=CC2=C(C=C1)NC(C=C2C)(C)C Ambient 4°C Soluble in ethanol. "Sadikot T, Swink M, Eskew JD, et al. Development of a high-throughput screening cancer cell-based luciferase refolding assay for identifying Hsp90 inhibitors. Assay Drug Dev Technol. 2013 Oct;11(8):478-88. PMID: 24127661.

?rnsrud R, Arukwe A, Bohne V, et al. Investigations on the metabolism and potentially adverse effects of ethoxyquin dimer, a major metabolite of the synthetic antioxidant ethoxyquin in salmon muscle. J Food Prot. 2011 Sep;74(9):1574-80. PMID: 21902931.

Kumar S, Engman L, Valgimigli L, et al. Antioxidant profile of ethoxyquin and some of its S, Se, and Te analogues. J Org Chem. 2007 Aug 3;72(16):6046-55. PMID: 17602530.

" Xn Not dangerous goods.

LKT E7329 Ethoxyquin 1 kg 567.6 Quinoline, food preservative; HSP90 inhibitor. 6-Ethoxy-1,2-dihydro-2,2,4-trimethylquinoline EMQ; Santoflex; Santoquin 91-53-2 ≥75% 217.31 C14H19NO CCOC1=CC2=C(C=C1)NC(C=C2C)(C)C Ambient 4°C Soluble in ethanol. "Sadikot T, Swink M, Eskew JD, et al. Development of a high-throughput screening cancer cell-based luciferase refolding assay for identifying Hsp90 inhibitors. Assay Drug Dev Technol. 2013 Oct;11(8):478-88. PMID: 24127661.

?rnsrud R, Arukwe A, Bohne V, et al. Investigations on the metabolism and potentially adverse effects of ethoxyquin dimer, a major metabolite of the synthetic antioxidant ethoxyquin in salmon muscle. J Food Prot. 2011 Sep;74(9):1574-80. PMID: 21902931.

Kumar S, Engman L, Valgimigli L, et al. Antioxidant profile of ethoxyquin and some of its S, Se, and Te analogues. J Org Chem. 2007 Aug 3;72(16):6046-55. PMID: 17602530.

" Xn Not dangerous goods.

LKT E7357 Esomeprazole Potassium 25 mg 111 (S) isomer of omeprazole; H+/K+ ATPase and MAO-A/B inhibitor. 6-methoxy-2-[(4-methoxy-3,5-dimethylpyridin-2-yl)methylsulfinyl]-1H-benzimidazole Omeprazole potassium 161796-84-5 ≥98% 383.51 C17H18N3O3S K _{CC1=CN=C(C(=C1OC)C)CS(=O)C2=NC3=C([N-]2)C=CC(=C3)OC.[K+] Ambient Ambient "Sugano K, Choi MG, Lin JT, et al. Multinational, double-blind, randomised, placebo-controlled, prospective study of esomeprazole in the prevention of recurrent peptic ulcer in low-dose acetylsalicylic acid users: the LAVENDER study. Gut. 2013 Dec 10. [Epub ahead of print]. PMID: 24326741.}

Costa-Rodrigues J, Reis S, Teixeira S, et al. Dose-dependent inhibitory effects of proton pump inhibitors on human osteoclastic and osteoblastic cell activity. FEBS J. 2013 Oct;280(20):5052-64. PMID: 23937530.

Petzer A, Pienaar A, Petzer JP. The inhibition of monoamine oxidase by esomeprazole. Drug Res (Stuttg). 2013 Sep;63(9):462-7. PMID: 23677700.

Marino ML, Fais S, Djavaheri-Mergny M, et al. Proton pump inhibition induces autophagy as a survival mechanism following oxidative stress in human melanoma cells. Cell Death Dis. 2010 Oct 21;1:e87. PMID: 21368860.

Saccar CL. The pharmacology of esomeprazole and its role in gastric acid related diseases. Expert Opin Drug Metab Toxicol. 2009 Sep;5(9):1113-24. PMID: 19606942.

" Not dangerous goods.

LKT E7357 Esomeprazole Potassium 100 mg 312.3 (S) isomer of omeprazole; H+/K+ ATPase and MAO-A/B inhibitor. 6-methoxy-2-[(4-methoxy-3,5-dimethylpyridin-2-yl)methylsulfinyl]-1H-benzimidazole Omeprazole potassium 161796-84-5 ≥98% 383.51 C17H18N3O3S K _{CC1=CN=C(C(=C1OC)C)CS(=O)C2=NC3=C([N-]2)C=CC(=C3)OC.[K+] Ambient Ambient "Sugano K, Choi MG, Lin JT, et al. Multinational, double-blind, randomised, placebo-controlled, prospective study of esomeprazole in the prevention of recurrent peptic ulcer in low-dose acetylsalicylic acid users: the LAVENDER study. Gut. 2013 Dec 10. [Epub ahead of print]. PMID: 24326741.}

Costa-Rodrigues J, Reis S, Teixeira S, et al. Dose-dependent inhibitory effects of proton pump inhibitors on human osteoclastic and osteoblastic cell activity. FEBS J. 2013 Oct;280(20):5052-64. PMID: 23937530.

Petzer A, Pienaar A, Petzer JP. The inhibition of monoamine oxidase by esomeprazole. Drug Res (Stuttg). 2013 Sep;63(9):462-7. PMID: 23677700.

Marino ML, Fais S, Djavaheri-Mergny M, et al. Proton pump inhibition induces autophagy as a survival mechanism following oxidative stress in human melanoma cells. Cell Death Dis. 2010 Oct 21;1:e87. PMID: 21368860.

Saccar CL. The pharmacology of esomeprazole and its role in gastric acid related diseases. Expert Opin Drug Metab Toxicol. 2009 Sep;5(9):1113-24. PMID: 19606942.

" Not dangerous goods.

LKT E7357 Esomeprazole Potassium 500 mg 1270.7 (S) isomer of omeprazole; H+/K+ ATPase and MAO-A/B inhibitor. 6-methoxy-2-[(4-methoxy-3,5-dimethylpyridin-2-yl)methylsulfinyl]-1H-benzimidazole Omeprazole potassium 161796-84-5 ≥98% 383.51 C17H18N3O3S K _{CC1=CN=C(C(=C1OC)C)CS(=O)C2=NC3=C([N-]2)C=CC(=C3)OC.[K+] Ambient Ambient "Sugano K, Choi MG, Lin JT, et al. Multinational, double-blind, randomised, placebo-controlled, prospective study of esomeprazole in the prevention of recurrent peptic ulcer in low-dose acetylsalicylic acid users: the LAVENDER study. Gut. 2013 Dec 10. [Epub ahead of print]. PMID: 24326741.}

Costa-Rodrigues J, Reis S, Teixeira S, et al. Dose-dependent inhibitory effects of proton pump inhibitors on human osteoclastic and osteoblastic cell activity. FEBS J. 2013 Oct;280(20):5052-64. PMID: 23937530.

Petzer A, Pienaar A, Petzer JP. The inhibition of monoamine oxidase by esomeprazole. Drug Res (Stuttg). 2013 Sep;63(9):462-7. PMID: 23677700.

Marino ML, Fais S, Djavaheri-Mergny M, et al. Proton pump inhibition induces autophagy as a survival mechanism following oxidative stress in human melanoma cells. Cell Death Dis. 2010 Oct 21;1:e87. PMID: 21368860.

Saccar CL. The pharmacology of esomeprazole and its role in gastric acid related diseases. Expert Opin Drug Metab Toxicol. 2009 Sep;5(9):1113-24. PMID: 19606942.

" Not dangerous goods.

LKT E7376 Estradiol 1 g 51.1 Endogenous steroid hormone, involved in regulation of menstrual cycle and growth of reproductive organs, used in HRT; ER agonist. (17β)-Estra-1,3,5(10)-triene-3,17-diol Dimenformon; Estrace; Estraderm; Evorel; Macrodiol; Menorest; Profoliol B; Systen; Vagifem; Zumenon 50-28-2 ≥97% 272.38 C18H24O2 CC12CCC3C(C1CCC2O)CCC4=C3C=CC(=C4)O Ambient Ambient Soluble in alcohol (35 mg/mL), acetone, dioxane, and other organic solvent. Insoluble in water. "Pentik?inen V, Erkkil? K, Suomalainen L, et al. Estradiol acts as a germ cell survival factor in the human testis in vitro. J Clin Endocrinol Metab. 2000 May;85(5):2057-67. PMID: 10843196.

Behl C, Widmann M, Trapp T, et al. 17-beta estradiol protects neurons from oxidative stress-induced cell death in vitro. Biochem Biophys Res Commun. 1995 Nov 13;216(2):473-82. PMID: 7488136.