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T6619Desmethyl Erlotinib hydrochloride；去甲厄洛替尼OSI420|||OSI-420|||DesMethyl Erlotinib (CP-473420) HCl|||CP-
Desmethyl Erlotinib hydrochloride (OSI 420) is an active metabolite of erlotinib which is an orally active EGFR tyrosin kinase inhibitor with IC50 of 2 and 20 nM for human EGFR and EGFR autophosphorylation in tumor cells.
价 格：￥电议型 号：T6619产 地：中国大陆
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T6549Isepamicin sulfate；硫酸异帕米星Isepamicine (Isepamycin|||Isepamicin Sulphate|||Isepacin|||sch21420) Sulpha
Isepamicin sulfate (sch21420) Sulphate) , an aminoglycoside antibacterial with good activity against strains producing type I 6-acetyltransferase, inhibits bacterial protein synthesis by targeting the bacterial 30S ribosomal subunit.
价 格：￥电议型 号：T6549产 地：中国大陆
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T65420Z-Lys(Z)-OH；化合物 Z-Lys(Z)-OHZ-Lys(Z)-OH
Z-Lys(Z)-OH is a useful organic compound for research related to life sciences. The catalog number is T65420 and the CAS number is 405-39-0.
价 格：￥电议型 号：T65420产 地：中国大陆
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T64420Chloro(crotyl)[di-tert-butyl(4-dimethylaminophenyl)phosphine]palladium(II)；化合物 Chloro(crotyl)[di-ter
Chloro(crotyl)[di-tert-butyl(4-dimethylaminophenyl)phosphine]palladium(II) is a useful organic compound for research related to life sciences and the catalog number is T64420.
价 格：￥电议型 号：T64420产 地：中国大陆
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T64209Anticancer agent 55；化合物 Anticancer agent 55Anticancer agent 55
Anticancer Agent is a potent anti-cancer agent that exhibits anti-cancer effects by inhibiting cell viability and cell migration in a dose-dependent manner and inducing apoptosis.Anticancer Agent has potential for prostate and breast cancer research.
价 格：￥电议型 号：T64209产 地：中国大陆
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T64208EZH2-IN-9；化合物 EZH2-IN-9EZH2-IN-9
EZH2-IN-9 is a potent inhibitor of EZH2, whose overexpression or mutations in the SET region (Y641F, Y641N, A687V, A677G point mutations) cause abnormal elevations in H3K27me3 and contribute to the growth and development of many tumours (e.g. breast cancer, prostate cancer, leukaemia, etc.). EZH2-IN-9 has shown potential for cancer research.
价 格：￥电议型 号：T64208产 地：中国大陆
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T64207FAK-IN-6；化合物 FAK-IN-6FAK-IN-6
FAK-IN-6 is a potent inhibitor of FAK (IC50: 1.415 nM). FAK-IN-6 exhibits anti-proliferative effects on certain cancer cell lines and can be used to study pancreatic cancer.
价 格：￥电议型 号：T64207产 地：中国大陆
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T64206VGD071；化合物 VGD071VGD071
VGD071, a compound that targets sortilin, presents a promising avenue for forthcoming research utilizing mouse models of breast cancer.
价 格：￥电议型 号：T64206产 地：中国大陆
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T64205HAMI 3379；化合物 HAMI 3379HAMI 3379
HAMI 3379 is a potent and selective CysLT2 receptor antagonist. HAMI 3379 exhibits protective effects against acute and subacute ischaemic brain injury and reduces microglia-associated inflammation.
价 格：￥电议型 号：T64205产 地：中国大陆
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T64204NU5455；化合物 NU5455NU5455
NU5455 is a selective, potent, orally active inhibitor of DNA-PKcs. NU5455 enhances the efficacy of locally released doxorubicin in liver tumour xenografts without causing any adverse effects. nU5455 enhances the efficacy and toxicity of topoisomerase inhibitors administered parenterally.
价 格：￥电议型 号：T64204产 地：中国大陆
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T64203T-Type calcium channel inhibitor 2；化合物 T-Type calcium channel inhibitor 2T-Type calcium channel inhi
T-Type calcium channel inhibitor 2 (compound 6g) is a potent inhibitor of the T-type calcium channel, acting on Cav3.1 (α1G) (IC50: 31.0 μM), Cav3.2 (α1H) (IC50: 83.1 μM), Cav3.3 (α1I) (α1H) ( T-Type calcium channel inhibitor 2 exhibited cytotoxicity against A549 and HCT-116 cells with IC50s of 5.0 and 6.4 μM, respectively.
价 格：￥电议型 号：T64203产 地：中国大陆
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T64202HCV-IN-40；化合物 HCV-IN-40HCV-IN-40
HCV-IN-39 (Compound 18a) is a potent, orally active nucleoside inhibitor of hepatitis C virus (HCV) that acts on the GT1a replicon (EC50: 0.259 μM), GT1b replicon (EC50: 0.434 μM) and GT1b CES1 replicon (EC50. 0.069 μM).
价 格：￥电议型 号：T64202产 地：中国大陆
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T64201Antibacterial agent 70；化合物 Antibacterial agent 70Antibacterial agent 70
Antibacterial agent 70 is a new dihydropyrimidinone-imidazole hybrid antimicrobial agent (MIC: 0.5 μg/ml).
价 格：￥电议型 号：T64201产 地：中国大陆
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T64200C5aR-IN-2；化合物 C5aR-IN-2C5aR-IN-2
C5aR-IN-2 is a potent inhibitor of C5aR. C5aR-IN-2 has shown potential for the study of inflammatory diseases.
价 格：￥电议型 号：T64200产 地：中国大陆
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T6420BMS-707035化合物BMS707035N-[(4-氟苯基)甲基1,6-二氢-5-羟基-1-甲基-6-氧代-2-(四氢-1,1-二氧-2H-1,2-噻嗪-2-基)-4-嘧啶甲酰胺
BMS-707035 is a specific HIV-I integrase (IN) inhibitor with IC50 of 15 nM. Phase 2.
价 格：￥电议型 号：T6420产 地：中国大陆
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T63444UNC4203；化合物 UNC4203UNC4203
UNC4203 is a potent, highly selective, orally active MERTK inhibitor that acts on MERTK (IC50: 1.2 nM), AXL (IC50: 140 nM), TYRO3 (IC50: 42 nM) and FLT3 (IC50: 90 nM).
价 格：￥电议型 号：T63444产 地：中国大陆
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T63420Antimycobacterial agent-2；化合物 Antimycobacterial agent-2Antimycobacterial agent-2
Antimycobacterial agent-2 is an effective anti-mycobacterial agent with a MIC99 of 0.8 μM against Mycobacterium tuberculosis (M.tb) H37Rv. Antimycobacterial agent-2 is cytotoxic, acting on CHO cells (IC50: 48.1 μM).
价 格：￥电议型 号：T63420产 地：中国大陆
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T6328Desmethyl Erlotinib；化合物Desmethyl ErlotinibOSI-420|||CP-473420|||O-Desmethyl Erlotinib；OSI-420|||CP-4
Desmethyl Erlotinib (CP-473420) is the active metabolite of Erlotinib (EGFR inhibitor with IC50 of 2 nM).
价 格：￥电议型 号：T6328产 地：中国大陆
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T6283Wortmannin；渥曼青霉素SL-2052|||KY-12420；SL-2052|||渥曼青霉素|||KY-12420
Wortmannin (SL-2052) is a PI3K inhibitor (IC50=3 nM) that is covalent and irreversible. Wortmannin is also an inhibitor of PlK1 and PlK3 (IC50=5.8/48 nM) that blocks autophagy.
价 格：￥电议型 号：T6283产 地：中国大陆
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T62420P2Y2R/GPR17 antagonist 1；P2Y2R/GPR17拮抗剂1P2Y2R/GPR17 antagonist 1
P2Y2R/GPR17 antagonist 1 (Compound 14m) is a dual P2Y2R (IC50: 3.17 μM) and GPR17 (IC50: 1.67 μM) antagonist.
价 格：￥电议型 号：T62420产 地：中国大陆
