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T23563ZM 226600；化合物ZM 226600ZM 226600
ZM 226600 is an ATP-sensitive potassium channel opener with an EC50 value of 500 nM. ZM226600 has an inhibitory effect on spontaneous bladder activity.
价 格：￥电议型 号：T23563产 地：中国大陆
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T23562ZK 93426 hydrochloride；化合物 T23562ZK 93426 hydrochloride
benzodiazepine receptor antagonist,competitive
价 格：￥电议型 号：T23562产 地：中国大陆
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T23560Zimelidine dihydrochloride；化合物 T23560Zimelidine dihydrochloride
5-HT re-uptake inhibitor
价 格：￥电议型 号：T23560产 地：中国大陆
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T2356Ro-3306；化合物Ro 3306Ro-3306
Ro 3306 is a CDK1 inhibitor that inhibits CDK1, CDK1/cyclin B1, and CDK2/cyclin E (Ki=20/35/340 nM) selectively and ATP-competitively. Ro-3306 exhibits antitumor activity, inhibits cell cycle arrest, and induces apoptosis.
价 格：￥电议型 号：T2356产 地：中国大陆
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T23559ZD-9379；化合物 T23559ZD 9379；ZD 9379
ZD-9379 is a NMDA receptor antagonist.
价 格：￥电议型 号：T23559产 地：中国大陆
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T23558ZD 7114 hydrochloride；化合物 T23558ZD 7114 hydrochloride
β3-adrenoceptor agonist
价 格：￥电议型 号：T23558产 地：中国大陆
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T23557Talibegron hydrochloride；Talibegron盐酸盐ZD2079 hydrochloride|||ZD 2079；ZD2079 hydrochloride|||ZD 2079
Talibegron hydrochloride (ZD2079 hydrochloride) is an β3 adrenergic receptor agonist with a pD2 of 3.72 on phenylephrine-preconstricted rat mesenteric artery. Relaxes rat mesenteric artery and isolated aorta in vitro. Inhibits ob gene expression and circulating leptin levels in lean mice in vivo.
价 格：￥电议型 号：T23557产 地：中国大陆
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T23555Z-VEID-FMK；化合物 T23555Z-VEID-FMK
When compared to other caspase inhibitors, Z-DRHD-FMK inhibited caspase 6 activity more effectively than the general caspase inhibitor of Z-Val-Ala-Asp (OMe)-fluoromethy ketone (Z-VAD-FMK) or the caspase 6 inhibitor Z-Val-Glu(Ome)-Ile-Asp(OMe)-fluoromethyl ketone.However, it was less effective in inhibiting TNFα-induced apoptosis than Z-VAD-FMK or Z-VEID-FMK, presumably.
价 格：￥电议型 号：T23555产 地：中国大陆
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T23554(Z)-FeCP-oxindole；化合物(Z)-FeCP-oxindole(Z)-FeCP-oxindole
(Z)-FeCP-oxindole is a selective inhibitor of VEGFR2 with an IC50 of 200 nM for human. (Z)-FeCP-oxindole shows anticancer activity.
价 格：￥电议型 号：T23554产 地：中国大陆
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T23552YZ9；化合物YZ9YZ9
Y29 is a potent PFKFB3 inhibitor with an IC50 of 0.183 ?M, and acts as a competitive inhibitor against Fru-6-P with a Ki of 0.094 ?M[1].
价 格：￥电议型 号：T23552产 地：中国大陆
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T23551YS-035 hydrochloride化合物 T23551YS 035 hydrochloride|||YS035 hydrochloride
inhibitor of outward K+ currents
价 格：￥电议型 号：T23551产 地：中国大陆
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T23550YM-750；化合物YM 750YM 750；YM 750
YM-750 is a potent inhibitor of acyl-CoA:cholesterol acyltransferase (ACAT), with an IC50 value of 0.18 μM. ACAT is an enzyme that catalyzes the conversion of cholesterol and long-chain fatty-acyl-coenzyme A into cholesteryl esters.
价 格：￥电议型 号：T23550产 地：中国大陆
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T2355CFTR(inh)-172；化合物CFTRinh-172CFTRinh 172|||CFTR Inhibitor-172|||CFTRinh-172|||CFTRinh172；CFTRinh 172|
CFTR(inh)-172 (CFTR Inhibitor-172) is a voltage-independent, selective CFTR inhibitor.
价 格：￥电议型 号：T2355产 地：中国大陆
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T23549YM 511；化合物YM 511YM 511
YM 511 is a highly specific non-steroidal aromatase inhibitor. YM 511 inhibits aromatase activities in microsomes from rat ovary and human placenta competitively (IC50s of 0.4 and 0.12 nM, respectively). YM 511 slightly inhibits production of other steroid hormones. YM 511 has the potential for suppressing estrogen-dependent action research without affecting serum levels of other steroid hormones.
价 格：￥电议型 号：T23549产 地：中国大陆
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T23548YM-298198 hydrochloride化合物 T23548YM 298198 hydrochloride
mGlu1 receptor antagonist
价 格：￥电议型 号：T23548产 地：中国大陆
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T23547YM 26734；化合物 T23547YM 26734
Competitive inhibitor of secretory phospholipase A2 (sPLA2)
价 格：￥电议型 号：T23547产 地：中国大陆
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T23546YM 244769 hydrochloride；化合物 T23546YM 244769 hydrochloride
inhibitor of the reverse mode of Na+/Ca2+ exchange (NCX)
价 格：￥电议型 号：T23546产 地：中国大陆
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