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T25282CYM 50358 hydrochloride (1314212-39-9 free base)；化合物 T25282CYM50358 hydrochloride|||CYM 50358 hydroc
CYM50358 HCl is an S1P4 antagonist.
价 格：￥电议型 号：T25282产 地：中国大陆
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T25269Colistin A；化合物 T25269Polymixin E1|||Polymyxin E1|||Colistin IV；Polymixin E1|||Polymyxin E1|||Colisti
Colistin A is an antibiotic generated by certain strains of the bacteria Paenibacillus polymyxa. Colistin is a mixture of the cyclic polypeptides colistin A and B and belongs to the class of polypeptide antibiotics known as polymyxins. Colistin is effective against most Gram-negative bacilli.
价 格：￥电议型 号：T25269产 地：中国大陆
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T24881Thymectacin；化合物 T24881NB 1011|||NB-1011|||NB1011；NB 1011|||NB-1011|||NB1011
Thymectacin is a small molecule phosphoramidite derivative of (E)-5-(2-bromovinyl)-2´-deoxyuridine with potential antineoplastic activity.
价 格：￥电议型 号：T24881产 地：中国大陆
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T24663YM928；化合物 T24663YM-928|||YM 928；YM-928|||YM 928
YM928 is an orally active antagonist of the AMPA receptor.
价 格：￥电议型 号：T24663产 地：中国大陆
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T24662YM 114；化合物 T24662YM-114|||Kae 393；YM-114|||Kae 393
YM 114 is an anatagonist of 5-HT(3) receptor.
价 格：￥电议型 号：T24662产 地：中国大陆
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T2445FG-2216；化合物FG-2216YM-311|||FG2216|||FG 2216；YM-311|||FG2216|||FG 2216
FG-2216 (YM-311) is a potent HIF-prolyl hydroxylase inhibitor for the PDH2 enzyme (IC50: 3.9 uM); orally bioavailable and induced reversible and significant Epo induction in vivo.
价 格：￥电议型 号：T2445产 地：中国大陆
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T24116GSM-1；化合物 T24116gamma Secretase modulator 1|||GSM 1 (enzyme modulator)|||J2.559.799K；gamma Secretase
GSM-1 is a modulator of γ-Secretase.
价 格：￥电议型 号：T24116产 地：中国大陆
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T23911CPS-11；化合物CPS-11CPS11|||CPS 11|||N-(Hydroxymethyl)thalidomide；CPS11|||CPS 11|||N-(Hydroxymethyl)thal
CPS-11 (N-(Hydroxymethyl)thalidomide) is a Thalidomide analogue that has significant antitumor activity and exhibits a wider range of activity and highly potent effects on the MM (multiple myeloma) cell line.
价 格：￥电议型 号：T23911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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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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T23544YM 202074化合物 T23544YM 202074
metabotropic glutamate receptor type 1 (mGlu1) antagonist
价 格：￥电议型 号：T23544产 地：中国大陆
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T2319Acotiamide monohydrochloride trihydrate盐酸阿考替胺Acotiamide hydrochloride|||YM-443 HCl|||盐酸阿考替胺|||Z-338
Acotiamide monohydrochloride trihydrate (Z-338 HCl) is the hydrochloride salt form of acotiamide, a prokinetic agent with gastrointestinal (GI) motility-enhancing activity. Although the exact mechanism by which acotiamide exerts its effect has yet to be fully elucidated, this agent appears to inhibit acetylcholinesterase (AchE), an enzyme responsible for the breakdown of acetylcholine (Ach). Increased Ach concentrations lead to an improvement of gastric emptying and GI motility and eventually to
价 格：￥电议型 号：T2319产 地：中国大陆
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T22718Desmethyl-YM 298198；化合物 T22718Desmethyl-YM 298198
mGlu1-selective antagonist
价 格：￥电议型 号：T22718产 地：中国大陆
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T22703CYM-5520；化合物CYM 5520CYM 5520；CYM 5520
CYM-5520 is a noncompetitive allosteric agonist of S1P2
价 格：￥电议型 号：T22703产 地：中国大陆
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T22702CYM 50769；化合物CYM 50769CYM 50769
CYM 50769 is a neuropeptide W/B receptor 1 (NPBWR1, GPR7) antagonist(IC50 = 0.12 μM). CYM 50769 inhibited NPW activation of NPBWR1 with a submicromolar IC50, and displayed high selectivity against a broad array of off-targets with pharmaceutical relevance.
价 格：￥电议型 号：T22702产 地：中国大陆
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T22526BML-111；化合物 T225265(S),6(R)-7-trihydroxymethyl Heptanoate；5(S),6(R)-7-trihydroxymethyl Heptanoate
inhibits leukotriene B4 (LTB4)-induced polymorphonuclear neutrophils (PMN) chemotaxis
价 格：￥电议型 号：T22526产 地：中国大陆
