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T16154MS417GTPL7512
MS417 is an inhibitor of BET-specific BRD4(BRD4-BD1 and BRD4-BD2 with IC50s of 30, 46 nM and Kds of 36.1, 25.4 nM, respectively), with weak selectivity at CBP BRD with IC50 of 32.7 μM.
价 格：￥电议型 号：T16154产 地：中国大陆
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T1549Raloxifene hydrochloride盐酸雷洛昔芬；Keoxifene hydrochloride；Raloxifene HCl；LY139481 hydrochloride；LY15675
Raloxifene hydrochloride is a second generation selective estrogen receptor modulator (SERM) used to prevent osteoporosis in postmenopausal women. It has estrogen agonist effects on bone and cholesterol metabolism but behaves as a complete estrogen antago
价 格：￥电议型 号：T1549产 地：中国大陆
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T15486HLM006474
HLM006474 is a pan inhibitor of E2F. This inhibits E2F4 DNA-binding (IC50: 29.8 μM in A375 cells).
价 格：￥电议型 号：T15486产 地：中国大陆
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T15485HJC0197
HJC0197 selectively blocks cAMP-induced Epac activation. HJC0197 is an effective exchange protein. Which straightly activated by cAMP (Epac) antagonist (IC50=5.9 μM for Epac2).
价 格：￥电议型 号：T15485产 地：中国大陆
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T15481HI-TOPK-032
HI-TOPK-032 is an effective and specific inhibitor of TOPK.
价 格：￥电议型 号：T15481产 地：中国大陆
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T15477Hexaminolevulinate hydrochloride5-氨基酮戊酸己酯盐酸盐；5-Aminolevulinic acid hexyl ester hydrochloride；P-1206；
Hexaminolevulinate hydrochloride has approved for cystoscopic detection of papillary bladder cancer and it also is a fluorescent agent.
价 格：￥电议型 号：T15477产 地：中国大陆
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T1547L-Cysteine methyl ester hydrochlorideL-半胱氨酸甲酯盐酸盐；L-Cysteine methyl ester hydrochloride(Acdrile)
Mecysteine hydrochloride is an antitussive and an expectorant agent, used to relieve breathing difficulties caused by mucus.
价 格：￥电议型 号：T1547产 地：中国大陆
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T15464HBX 19818
HBX 19818 is a specific ubiquitin-specific protease 7 (USP7) inhibitor (IC50: 28.1 μM).
价 格：￥电议型 号：T15464产 地：中国大陆
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T1546Nitazoxanide硝唑尼特；NSC 697855
Nitazoxanide is a synthetic benzamide with antiprotozoal activity. Nitazoxanide exerts its antiprotozoal activity by interfering with the pyruvate ferredoxin/flavodoxin oxidoreductase dependent electron transfer reaction.
价 格：￥电议型 号：T1546产 地：中国大陆
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T15454GW843682XGW843682
GW843682X is a selective and ATP-competitive inhibitor of PLK1 and PLK3 (IC50s: 2.2 nM and 9.1 nM, respectively). It is also >100-fold selective against ～30 other kinases.
价 格：￥电议型 号：T15454产 地：中国大陆
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T15453GW76472-[[4-[2-[[环己基氨基)羰基](4-环己基丁基)氨基]乙基]苯基]硫基]-2-甲基丙酸
GW7647 is a potent agonist of PPARα (EC50s: 6 nM, 1.1 μM, and 6.2 μM for human PPARα, PPARγ, and PPARδ, respectively).
价 格：￥电议型 号：T15453产 地：中国大陆
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T15451GW-870086
GW-870086 is an effective anti-inflammatory agent. GW-870086 also plays a role in a glucocorticoid receptor agonist (pIC50: 10.1 in A549 cells expressing NF-κB).
价 格：￥电议型 号：T15451产 地：中国大陆
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T1545LevamlodipineS-amlodipine；(S)-Amlodipine；左旋氨氯地平
Levamlodipine belongs to the dihydropyridine group of calcium channel blockers. Levamlodipine, also known as S-amlodipine, is a pharmacologically active enantiomer of amlodipine, an antihypertensive and anti-anginal medication. The names S-amlodipine and
价 格：￥电议型 号：T1545产 地：中国大陆
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T15447Guacetisal
Guacetisal is extracted from the esterification reaction of acetylsalicylic acid with guaiacol which can be used for research on the treatment of chronic bronchitis.
价 格：￥电议型 号：T15447产 地：中国大陆
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T15445ProxalutamideGT0918
Proxalutamide is a potent antagonist of the androgen receptor (AR).
价 格：￥电议型 号：T15445产 地：中国大陆
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T1544Olsalazine disodium奥沙拉秦钠；Olsalazine Sodium；Dipentum
Olsalazine sodium is bioconverted to 5-aminosalicylic acid (5-ASA) in the colon and has anti-inflammatory activity in ulcerative colitis.
价 格：￥电议型 号：T1544产 地：中国大陆
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T15437GSK3145095
GSK3145095 is an orally active inhibitor of RIPK1 with IC50 of 5 nM, with potential immunomodulatory activities and antineoplastic.
价 格：￥电议型 号：T15437产 地：中国大陆
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T15436GSK2838232
GSK2838232 inhibit HIV reverse transcriptase activity across a broad panel of HIV-1 isolates,GSK2838232 is novel human immune virus (HIV) maturation inhibitor.
价 格：￥电议型 号：T15436产 地：中国大陆
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T15435GSK2837808A
GSK2837808A is a potent and selective inhibitor of lactate dehydrogenase A (LDHA) (IC50s: 1.9 and 14 nM for LDHA and LDHB, respectively).
价 格：￥电议型 号：T15435产 地：中国大陆
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T15433GSK2795039
GSK2795039 inhibits reactive oxygen species (ROS) production and NADPH consumption. GSK2795039 decreases apoptosis. GSK2795039 is an inhibitor of NADPH oxidase 2 (NOX2) (pIC50: 6 in different cell-free assays).
价 格：￥电议型 号：T15433产 地：中国大陆
