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T60742HIV-1 integrase inhibitor 8
HIV-1 integrase inhibitor 8 is an inhibitor of HIV-1 integrase. Integration is a required step in HIV replication [1].
价 格：￥电议型 号：T60742产 地：中国大陆
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T8989NCGC 607inhibit,Glucosidase,NCGC-607,NCGC 607,Inhibitor
NCGC607 is a a noninhibitory chaperone of glucocerebrosidase (GCase).
价 格：￥电议型 号：T8989产 地：中国大陆
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TP1993LM617 acetateM617 acetate,M-617 acetate(860790-38-1 Free base )
M617 acetate is a selective agonist of galanin receptor 1 (GAL1). M617 acetate acts through central GAL1, promotes GLUT4 expression, and enhances GLUT4 content in the cardiac muscle of type 2 diabetic rats. The Ki values are 0.23 and 5.71 nM for GAL1 and GAL2, respectively.
价 格：￥电议型 号：TP1993L产 地：中国大陆
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T60757SB-216
SB-216 is able to be used for the research of cancer which is a potent inhibitor of tubulin polymerization. SB-216 exhibits strong antiproliferative potency in a panel of human cancer cell lines, including melanoma, breast cancer, and lung cancer [1].
价 格：￥电议型 号：T60757产 地：中国大陆
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T6607Nitenpyraminhibit,nAChR,Inhibitor,Nicotinic acetylcholine receptors,Nitenpyram
Nitenpyram is a nicotinic acetylcholine receptor (AchR) agonist, used as veterinary medicine to treat parasites of livestock and pets.
价 格：￥电议型 号：T6607产 地：中国大陆
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T8607NSC 139486NSC 139486
M-084 hydrochloride is a blocker of TRPC4/5 channel, with antidepressant and anxiolytic effects.
价 格：￥电议型 号：T8607产 地：中国大陆
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T67845ARUK2001607
ARUK2001607 is a selective inhibitor of phosphatidylinositol 5-phosphate 4-kinase γ (PI5P4Kγ, Kd= 7.1 nM). ARUK2001607 exhibits high selectivity over other >150 kinases.
价 格：￥电议型 号：T67845产 地：中国大陆
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TP1112LLH-RH, salmon acetate(86073-88-3 free base)LHRH, salmon acetate(86073883 free base),LH RH, salmon ac
Luteinizing Hormone Releasing Hormone (LH-RH) acetateis a pituitary Hormone synthesized in the hypothalamus and plays a crucial role in the control of reproductive function.
价 格：￥电议型 号：TP1112L产 地：中国大陆
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T6079NVP-ADW742GSK 552602A；ADW；ADW742
NVP-ADW742 is an IGF-1R inhibitor with IC50 of 0.17 μM, >16-fold more potent against IGF-1R than InsR; little activity to HER2, PDGFR, VEGFR-2, Bcr-Abl and c-Kit.
价 格：￥电议型 号：T6079产 地：中国大陆
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T6078SaracatinibAZD0530；塞卡替尼
Saracatinib (AZD0530) is an effective Src inhibitor (IC50: 2.7 nM), and effective to Lck, Fyn, Lyn, Blk, Fgr and c-Yes.
价 格：￥电议型 号：T6078产 地：中国大陆
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T6077ZM-447439ZM 447439
ZM 447439 is a selective and ATP-competitive inhibitor for Aurora A and Aurora B with IC50 of 110 nM and 130 nM, respectively. It is more than 8-fold selective for Aurora A/B than MEK1, Src, Lck and has little effect against CDK1/2/4, Plk1, Chk1, etc.
价 格：￥电议型 号：T6077产 地：中国大陆
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T6076EPZ015666GSK3235025
EPZ015666 is an orally available inhibitor of PRMT5 enzymatic activity.
价 格：￥电议型 号：T6076产 地：中国大陆
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T6075Epothilone B帕妥匹隆；EPO 906；Patupilone
Epothilone B is a compound isolated from the myxobacterium Sorangium cellulosum. Similar to paclitaxel, patupilone induces microtubule polymerization and stabilizes microtubules against depolymerization conditions. In addition to promoting tubulin polymer
价 格：￥电议型 号：T6075产 地：中国大陆
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T6074KPT276KPT-276；KPT 276
KPT-276 is an orally bioavailable selective inhibitor of nuclear export (SINE) that irreversibly bind to CRM1 and block the function of CRM1.
价 格：￥电议型 号：T6074产 地：中国大陆
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T6073OG-L002
OG-L002 is an effective and selective LSD1 inhibitor (IC50: 20 nM), showing 69- and 36-fold selectivity over MAO-A and MAO-B, respectively.
价 格：￥电议型 号：T6073产 地：中国大陆
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T6072LBGT226BGT226 free base；NVP-BGT226
Bgt226 is a novel dual PI3K / mTOR inhibitor, it acts on PI3K α/β/γ with IC50 of 4 nM / 63 nM / 38 nM, respectively.
价 格：￥电议型 号：T6072L产 地：中国大陆
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T6072BGT226 maleateNVP-BGT226 (maleate)；NVP-BGT226；BGT226
BGT226 (NVP-BGT226) is a class I PI3K/mTOR inhibitor for PI3Kα/β/γ (IC50: 4/63/38 nM) .
价 格：￥电议型 号：T6072产 地：中国大陆
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T6071ParbendazoleSKF 29044；帕苯咪唑
Parbendazole is a potent inhibitor of microtubule assembly(EC50 : 8.79 nM).Parbendazole is a carbamate ester-amine. It finds applications in control or treatment of nematode infestations.
价 格：￥电议型 号：T6071产 地：中国大陆
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T6070ON-01910N-[2-甲氧基-5-[[[2-(2,4,6-三甲氧基苯基)乙烯基]磺酰]甲基]苯基]甘氨酸钠盐
ON-01910 is a non-ATP-competitive PLK1 inhibitor(IC50 of 9 nM, in a cell-free assay). It shows 30-fold greater selectivity against Plk2 and no activity to Plk3. Rigosertib inhibits PI3K/Akt pathway and activates oxidative stress signals. Rigosertib induce
价 格：￥电议型 号：T6070产 地：中国大陆
