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T23776BBMP；化合物 T23776BBMP
BBMP is an inhibitor of mitochondrial permeability transition pore.
价 格：￥电议型 号：T23776产 地：中国大陆
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T23686AHR-activator-1023；化合物 T23686Branching Morphogenesis Modulator 1023|||Cpd 1023|||Compound 1023|||BMM
AHR-activator-1023 is the aryl hydrocarbon receptor activator. It is also a specific FGF2-induced branching morphogenesis modulator.
价 格：￥电议型 号：T23686产 地：中国大陆
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T2349BMS-754807；化合物BMS-754807BMS-754807
Dual IGF-1R/InsR Inhibitor BMS-754807 is an oral small molecule inhibitor of insulin-like growth factor 1 receptor (IGF-1R) and insulin receptor (InsR) tyrosine kinases with potential antineoplastic activity.
价 格：￥电议型 号：T2349产 地：中国大陆
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T2337BMS-303141；化合物BMS-303141BMS 303141；BMS 303141
BMS-303141 is a potent ATP-citrate lyase (ACL) inhibitor (IC50: 0.13 uM, human recombinant ACL).
价 格：￥电议型 号：T2337产 地：中国大陆
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T2299BMS-833923；化合物BMS-833923XL-139；XL-139
BMS-833923 (XL-139), an orally bioavailable Smoothened antagonist, inhibits BODIPY cyclopamine binding to SMO in a dose-dependent manner (IC50: 21 nM).
价 格：￥电议型 号：T2299产 地：中国大陆
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T22911β-N-methylamino-L-alanine hydrochloride化合物L-BMAA hydrochlorideL-BMAA hydrochloride
β-N-methylamino-L-alanine hydrochloride (L-BMAA hydrochloride) is a neurotoxin produced by cyanobacteria. L-BMAA hydrochloride could cause amyotrophic lateral sclerosis (ALS) and possibly other neurodegenerative diseases.
价 格：￥电议型 号：T22911产 地：中国大陆
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T22710DBM 1285 dihydrochloride；化合物 T22710DBM 1285 dihydrochloride
DBM 1285 dihydrochloride is a p38 MAPK inhibitor.
价 格：￥电议型 号：T22710产 地：中国大陆
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T22612BMY-14802 hydrochloride；化合物BMY-14802盐酸盐BMS 181100 hydrochloride|||BMY-14802-1|||BMY 14802 hydrochlor
BMY-14802 hydrochloride (BMS 181100 hydrochloride) is a selective antagonist of σ receptor (IC50 = 112 nM) with antipsychotic effects. BMY-14802 hydrochloride is an agonist of the α1-adrenergic receptor and 5-HT1A.
价 格：￥电议型 号：T22612产 地：中国大陆
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T22611BMS 961；化合物 T22611BMS 961
BMS961 is a potent and selective retinoic acid receptor gamma (RARγ) agonist (IC50: 30 nM).
价 格：￥电议型 号：T22611产 地：中国大陆
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T22609BMS-378806；化合物 T22609BMS-378806
BMS-378806 is a novel attachment inhibitor of HIV (EC50: 2.68±1.64nM, 26.5±3.5nM, 2.94±2.01nM,15.5±6.8nM, 3.46±0.81nM, 1.47±0.63nM and 0.85±0.13nM for LAI(T), SF-2(T),NL4-3(T), Bal(M), SF-162(M), JRFL(M) and TLAV(dual), respectively).
价 格：￥电议型 号：T22609产 地：中国大陆
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T22608BMS 193885；化合物BMS193885BMS193885；BMS193885
BMS 193885 is a selective and competitive neuropeptide Y(1) receptor antagonist with affinity of 3.3 nM.
价 格：￥电议型 号：T22608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
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T2241Alisertib；化合物AlisertibMLN 8237；MLN 8237|||4-[[9-氯-7-(2-氟-6-甲氧基苯基)-5H-嘧啶并[5,4-D][2]苯并氮杂卓-2-基]氨基]-2-甲氧
Alisertib (MLN 8237) is an Aurora A kinase inhibitor (IC50=1.2 nM) with oral activity and selectivity. Alisertib has antitumor activity, induces apoptosis and autophagy, and induces cell cycle arrest.
价 格：￥电议型 号：T2241产 地：中国大陆
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T22303Dasatinib hydrochloride；达沙替尼盐酸盐BMS-354825 HCl；BMS-354825 HCl
Dasatinib hydrochloride (BMS-354825 HCl) (BMS-354825) hydrochloride is a highly potent, ATP competitive, orally active dual Src/Bcr-Abl inhibitor with potent antitumor activity. The Kis are 16 pM and 30 pM for Src and Bcr-Abl, respectively. Dasatinib hydrochloride hydrochloride inhibits Bcr-Abl and Src with IC50s of <1.0 nM and 0.5 nM, respectively. Dasatinib hydrochloride hydrochloride also induces Apoptosis and Autophagy.
价 格：￥电议型 号：T22303产 地：中国大陆
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T22277BMS-P5；化合物BMS-P5BMS-P5
BMS-P5 is a specific and orally active Peptidylarginine Deiminase 4 (PAD4) inhibitor.
价 格：￥电议型 号：T22277产 地：中国大陆
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T22276Bis(maltolato)oxovanadium(IV)；双(麦芽醇)氧钒(IV)BMOV|||Bis maltolato oxovanadium,Bis(maltolato)oxovanadium
Bis(maltolato)oxovanadium(IV) (BMOV) is a potent, reversible, competitive and orally active pan-PTP (protein tyrosine phosphatases)inhibitor with insulin-mimicking effects and anti-diabetic properties. BMOV is a potent insulin sensitize. BMOV is shown to improve cardiac dysfunctions in diabetic models. BMOV inhibits HCPTPA, PTP1B, HPTPβ and SHP2 with IC50s of 126 nM, 109 nM, 26 nM and 201 nM, respectivelyr[1][2].
价 格：￥电议型 号：T22276产 地：中国大陆
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T22192BMS 195614；化合物BMS 195614BMS614；BMS614
BMS 195614 (BMS614) is a selective RARα antagonist. BMS 195614 can bind to the RARα subunit.
价 格：￥电议型 号：T22192产 地：中国大陆
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T22049BMS 753；化合物BMS 753BMS 753
BMS 753 is an agonist of isotype-selective retinoic acid receptor α (RARα, Ki= 2 nM).
价 格：￥电议型 号：T22049产 地：中国大陆
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T21790BMS 182874 hydrochloride；化合物BMS 182874 hydrochlorideBMS 182874 hydrochloride
BMS 182874 hydrochloride is a nonpeptide endothelin (El) receptor antagonist.
价 格：￥电议型 号：T21790产 地：中国大陆
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T21714BMS453化合物BMS 453BMS 453|||BMS-189453
BMS453 (BMS-189453), a synthetic retinoid, is a potent and selective agonist of RARβ and a potent testicular toxin. BMS453 inhibits breast cell growth predominantly through the induction of active TGFβ.
价 格：￥电议型 号：T21714产 地：中国大陆
