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T3235Rebaudioside A瑞鲍迪甙 A；莱苞迪甙 A；Stevioside A3；Glycoside A3；Reb A；Reb-A 97
Rebaudioside A is a novel agent of glycoside clathration of pharmacons, acts as α-glucosidase inhibitor.
价 格：￥电议型 号：T3235产 地：中国大陆
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T26235SulfaperinIsosulfamerazine；Methylsulfadiazin；Anastaf；Chemiopen；Archisulfa；Demosulfan；磺胺培林
Sulfaperin is a sulfonamide antibacterial agent.
价 格：￥电议型 号：T26235产 地：中国大陆
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T2511Plinabulin普那布林；NPI-2358
Plinabulin (NPI-2358) is a vascular disrupting agent (VDA) against tubulin-depolymerizing tumor cells ( IC50: 9.8-18 nM). Plinabulin selectively targets and binds to the colchicine-binding site of tubulin, thereby interrupting equilibrium of microtubule d
价 格：￥电议型 号：T2511产 地：中国大陆
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T2359ANA-12ANA12；ANA 12
ANA-12 is a potent and selective TrkB antagonist with anxiolytic and antidepressant activity in mice.
价 格：￥电议型 号：T2359产 地：中国大陆
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T2356Ro-3306Ro 3306
RO-3306 is a selectivity ATP-competitive CDK1 inhibitor (Ki: 20 nM). The selectivity of RO-3306 for CDK1 is >15-fold higher than a diverse panel of human kinases.
价 格：￥电议型 号：T2356产 地：中国大陆
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T23552YZ9
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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T23550YM-750YM 750
YM-750 is a potent acyl-CoA:cholesterol acyltransferase (ACAT) inhibitor (IC50=0.18 μM). ACAT catalyzes the formation of cholesteryl esters from cholesterol and long-chain fatty-acyl-coenzyme A.
价 格：￥电议型 号：T23550产 地：中国大陆
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T2355CFTR(inh)-172CFTR Inhibitor-172；CFTRinh172；CFTRinh-172；CFTRinh 172
CFTRinh-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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T2353BRD7116BRD7716
BRD7116 competitively binds to bacterial DNA gyrase, with cell-non-autonomous anti-leukemia activity.
价 格：￥电议型 号：T2353产 地：中国大陆
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T23524W-84 dibromideHDMPPA
W-84 dibromide is a M2-receptor selective modulator.
价 格：￥电议型 号：T23524产 地：中国大陆
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T23521VULM 1457
VULM 1457 is a potent ACAT inhibitor. VULM 1457 has remarkable hypolipidaemic activity and improves the overall myocardial ischaemia-reperfusion injury outcomes. VULM1457 significantly reduces production and secretion of adrenomedullin (AM) and down-regul
价 格：￥电议型 号：T23521产 地：中国大陆
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T2352AMI-1AMI 1；AMI1
AMI-1 is an effective and selective Histone Methyltransferase (HMT) inhibitor (IC50: 3.0/8.8 μM, for yeast Hmt1p, and human PRMT1).
价 格：￥电议型 号：T2352产 地：中国大陆
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T23515VU-29VU 29
VU-29 is a positive allosteric mGlu5 receptor modulator with EC50=9 nM and Ki=244 nM for rmGluR5. It is selective for mGluR5 relative to other mGluR subtypes (EC50: rmGluR1/rmGluR2=557 nM/1.5 μM; hmGluR4=154 nM).
价 格：￥电议型 号：T23515产 地：中国大陆
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T23513VU10010VU 10010
VU 10010 is allosteric potentiator of M4 acetylcholine receptors.
价 格：￥电议型 号：T23513产 地：中国大陆
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T2351FasiglifamTAK875
TAK875 is a potent, selective and orally bioavailable GPR40 agonist.
价 格：￥电议型 号：T2351产 地：中国大陆
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T23508VU 0255035
VU 0255035 is a highly selective, competitive and brain penetrant muscarinic M1 receptor antagonist with an IC50 of 130 nM. It reduces pilocarpine-induced seizures in mice. It is used to examine the role of the M1 receptor in diverse situations.
价 格：￥电议型 号：T23508产 地：中国大陆
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T2350MALT1 inhibitor MI-2MI 2 (MALT1 inhibitor)；MALT1 inhibitor；MI 2
MI-2 (MALT1 inhibitor) is an irreversible MALT1 inhibitor.
价 格：￥电议型 号：T2350产 地：中国大陆
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T22359MDL 100009
MDL 100009, the S-enantiomer of MDL 100151 and the opposite enantiomer of MDL 100907, is a selective antagonist of 5-HT2A.
价 格：￥电议型 号：T22359产 地：中国大陆
