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T10895CSN5i-3；化合物CSN5i-3CSN5i-3
CSN5i-3 is a novel potent oral and selective CSN5/Jab1 inhibitor that inhibits CSN-catalyzed Cul1 deneddylation with an IC50 value of 5.8 nM.CSN5i-3 exhibits anticancer activity, inhibits cell proliferation and induces apoptosis in human breast cancer cells.
价 格：￥电议型 号：T10895产 地：中国大陆
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T1084Apramycin sulfate；硫酸安普霉素Nebramycin II|||Ai3-29795；Nebramycin II|||Ai3-29795|||硫酸安普霉素|||硫酸阿布拉霉素
Apramycin sulfate (Nebramycin II) is an aminoglycoside antibiotic.
价 格：￥电议型 号：T1084产 地：中国大陆
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T10795Chlordantoin；氯登妥因Clodantoin；Clodantoin|||氯登妥因
Chlordantoin is an antifungal agent with the potential for vaginal candidiasis treatment.
价 格：￥电议型 号：T10795产 地：中国大陆
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T10784CH6953755；化合物CH6953755CH6953755
CH6953755 is an orally active, potent and selective YES1 kinase inhibitor (IC50:1.8 nM).CH6953755 has anticancer activity and inhibits cancer cell proliferation by inhibiting YES1 kinase.
价 格：￥电议型 号：T10784产 地：中国大陆
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T10759CEP-28122 mesylate salt (1022958-60-6 free base)；化合物CEP-28122 mesylate saltCEP-28122 mesylate salt；C
CEP-28122 mesylate salt (1022958-60-6 free base) is a highly selective orally active ALK inhibitor (IC50: 1.9 nM in an enzyme-based TRF assay).
价 格：￥电议型 号：T10759产 地：中国大陆
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T10699L2CBB1007 trihydrochloride (1379573-92-8 free base)；化合物 T10699L2CBB1007 trihydrochloride；CBB1007 trihy
CBB1007 trihydrochloride is a selective, reversible, and substrate competitive LSD1 inhibitor (IC50: 5.27 μM for hLSD1).
价 格：￥电议型 号：T10699L2产 地：中国大陆
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T10699CBB1007 hydrochloride (1379573-92-8 free base)；化合物 T10699CBB1007 hydrochloride；CBB1007 hydrochloride
CBB1007 Hcl is a selective, reversible, and substrate competitive LSD1 inhibitor (IC50: 5.27 μM for hLSD1).
价 格：￥电议型 号：T10699产 地：中国大陆
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T10698LCBB1003 hydrochloride (1379573-88-2 free base)；化合物 T10698LCBB1003 hydrochloride；CBB1003 hydrochlorid
CBB1003 hydrochloride is a new inhibitor of histone demethylase LSD1 (IC50: 10.54 μM).
价 格：￥电议型 号：T10698L产 地：中国大陆
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T10695CB1151；化合物 T10695CB1151
CB1151 is a 20-epi analogue of 1,25 dihydroxyvitamin D3 with anti-tumor effects. It inhibits MCF-7 cell growth (IC50: 0.82 nM).
价 格：￥电议型 号：T10695产 地：中国大陆
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T10692CB-1158 dihydrochloride (2095732-06-0 free base)；化合物 T10692INCB01158 dihydrochloride|||CB-1158 dihyd
CB-1158 dihydrochloride is an effective and orally active inhibitor of arginase (IC50s: 86 nM and 296 nM for recombinant human arginase 1 and 2).
价 格：￥电议型 号：T10692产 地：中国大陆
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T10691CAY10595；化合物CAY10595CAY10595
CAY10595 is an antagonist of the CRTh2 (DP2) receptor with a Ki of 10 nM.
价 格：￥电议型 号：T10691产 地：中国大陆
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T10595LBQ-788 sodium salt；化合物 T10595LBQ-788 sodium salt
BQ-788 sodium salt is a potent and selective antagonist of ETB receptor(ETB receptors with an IC50 of 1.2 nM in human Girrardi heart cells).
价 格：￥电议型 号：T10595L产 地：中国大陆
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T10595BQ-788；化合物BQ-788BQ788；BQ788
BQ-788 is a selective and potent ETB receptor antagonist with potential hypertensive activity.BQ-788 inhibits ET-1 binding to ETB receptors and inhibits exogenous ET-1-induced elevation of coronary artery perfusion pressure.
价 格：￥电议型 号：T10595产 地：中国大陆
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T10577BM 957；化合物 T10577BM 957
BM 957 is an effective Bcl-2 and Bcl-xL inhibitor (Kis: 1.2 and <1 nM; IC50s: 5.4 and 6.0 nM).
价 格：￥电议型 号：T10577产 地：中国大陆
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T10566BMS-191095；化合物BMS-191095BMS-191095
BMS-191095 is mitochondrial ATP-sensitive potassium (mitoKATP) channel activator.
价 格：￥电议型 号：T10566产 地：中国大陆
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T10495LBefiradol化合物 T10495LNLX-112|||F13640
Befiradol (NLX-112) is an agonist of 5-HT1A receptor.
价 格：￥电议型 号：T10495L产 地：中国大陆
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T10468Elimusertib hydrochloride(1876467-74-1 free base)；化合物 Elimusertib hydrochlorideBAY-1895344 hydrochlo
Elimusertib hydrochloride(1876467-74-1 free base) (BAY-1895344 hydrochloride) is a effective, orally available and selective ATR inhibitor with anti-tumor activity.
价 格：￥电议型 号：T10468产 地：中国大陆
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T10395LATM-3507化合物 ATM-3507ATM3507|||ATM 3507
ATM-3507 is a protomyosin inhibitor with anticancer activity that inhibits human melanoma and can be used to study ovarian cancer.
价 格：￥电议型 号：T10395L产 地：中国大陆
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T10395ATM-3507 trihydrochloride (1861449-70-8 free base)；化合物 T10395ATM-3507 trihydrochloride；ATM-3507 trih
ATM-3507 trihydrochloride is a potent tropomyosin inhibitor (IC50s: 3.83-6.84 μM in human melanoma cell lines).
价 格：￥电议型 号：T10395产 地：中国大陆
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T10338Antisauvagine-30 TFA (220673-95-0 free base)；化合物 T10338Antisauvagine-30 TFA|||aSvg-30 TFA；Antisauvag
Antisauvagine-30 TFA (aSvg-30 TFA) is a highly selective and competitive antagonist of CRF2 receptor peptidic. It shows a Kd of 1.4 nM and 150 nM for mCRFR2β and CRFR1, respectively.
价 格：￥电议型 号：T10338产 地：中国大陆
