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T26370(25S)-delta7-Dafachronic acid；化合物 T26370(25S)-delta7-Dafachronic acid
(25S)-delta7-Dafachronic acid, an orphan nuclear receptor DAF-12 ligand, inhibits the dauer-promoting activity of DAF-12.
价 格：￥电议型 号：T26370产 地：中国大陆
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T26363LNapitane；萘吡坦A75200|||A-75200|||A 75200|||ABT 200；A75200|||A-75200|||A 75200|||ABT 200
napitane (A 75200) is a novel catecholamine uptake inhibitor with inhibitory effects on α-adrenergic receptors and potential antidepressant activity for the study of depression.
价 格：￥电议型 号：T26363L产 地：中国大陆
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T23947DA-7867；化合物 T23947UNII-491MT9GU8K|||DA 7867|||DA7867；UNII-491MT9GU8K|||DA 7867|||DA7867
DA-7867 is a novel oxazolidinone. DA-7867 had the lowest MIC for 90% of the aerobic gram-positive bacterial strains tested (≤0.25 μg/ml) and it was more potent than linezolid. DA-7867 was the most active drug with a MIC(90) of 0.125 μg/ml.
价 格：￥电议型 号：T23947产 地：中国大陆
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T21782A 77636 hydrochloride；盐酸A77636A77636 hydrochloride；盐酸A77636|||A77636 hydrochloride
A 77636 hydrochloride is a potent, orally active, selective and long acting dopamine D1 receptor agonist (pKi=7.40; Ki=39.8 nM). A 77636 hydrochloride shows antiparkinsonian activity. A 77636 hydrochloride is functionally inactive at dopamine D2 receptor.
价 格：￥电议型 号：T21782产 地：中国大陆
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T21422Methylnaltrexone bromide；溴化甲基纳曲酮Relistor|||MOA-728|||MOA 728|||Methylnaltrexone|||MOA728；Relistor|||
Methylnaltrexone bromide (MOA-728) is one of the newer agents of peripherally-acting μ-opioid antagonists. Methylnaltrexone bromide acts to reverse some of the side effects of opioid drugs such as constipation without affecting analgesia or precipitating withdrawals.
价 格：￥电议型 号：T21422产 地：中国大陆
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T2113PHA-793887；化合物PHA-793887PHA 793887|||PHA793887；PHA 793887|||PHA793887
PHA-793887 has been used in trials studying the treatment of Advanced/Metastatic Solid Tumors.
价 格：￥电议型 号：T2113产 地：中国大陆
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T2098A 77-01；化合物A77-01A77-01；A77-01
A 77-01 is a potent inhibitor of TGF-(beta) type I receptor superfamily activin-like kinase ALK5 with IC50 of 25 nM.
价 格：￥电议型 号：T2098产 地：中国大陆
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T20580Picolinamidoxime；化合物 T20580RA7|||RA-7|||RA 7|||Picolinamide oxime；RA7|||RA-7|||RA 7|||Picolinamide o
Picolinamidoxime is a biochemical substance.
价 格：￥电议型 号：T20580产 地：中国大陆
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T1782LCanagliflozin hemihydrate；卡格列净半水合物JNJ28431754|||TA 7284|||TA7284|||TA-7284|||JNJ 28431754|||JNJ-2843
Canagliflozin hemihydrate (TA 7284) is a drug of the gliflozin class or subtype 2 sodium-glucose transport inhibitors used for the treatment of type 2 diabetes. SGLT2 is responsible for at least 90% of renal glucose reabsorption (SGLT1 being responsible for the remaining 10%). Blocking this transporter causes up to 119 grams of blood glucose per day to be eliminated through the urine, corresponding to 476 kilocalories.
价 格：￥电议型 号：T1782L产 地：中国大陆
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T13284LVapendavir；化合物 T13284LBTA798；BTA798
Vapendavir is a potent enteroviral capsid binder. Vapendavir has an effective antiviral activity for enterovirus 71 replication (EC50: 0.5-1.4 μM in different EV71 strains).
价 格：￥电议型 号：T13284L产 地：中国大陆
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T13284Vapendavir diphosphate；化合物 T13284BTA798 diphosphate；BTA798 diphosphate
Vapendavir diphosphate is a potent enteroviral capsid binder (CB) and has a potent antiviral activity for enterovirus 71 (EV71) replication (EC50: 0.5-1.4 μM in different EV71 strains).
价 格：￥电议型 号：T13284产 地：中国大陆
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T12827SA72；化合物 T12827SA72
SA72 is a highly selective inhibitor of fatty acid amide hydrolase (FAAH).
价 格：￥电议型 号：T12827产 地：中国大陆
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T125439Calystegine A7；化合物 Calystegine A7Calystegine A7
Calystegine A7 is a useful organic compound for research related to life sciences and the catalog number is T125439.
价 格：￥电议型 号：T125439产 地：中国大陆
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T1245147-Dehydrobrefeldin A；化合物 7-Dehydrobrefeldin A7-Dehydrobrefeldin A
产品可用于生物细胞实验
价 格：￥电议型 号：T124514产 地：中国大陆
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T10214A7132；化合物A7132A7132
A7132 is an antibacterial agent and possesses broad and potent antibacterial activity.
价 格：￥电议型 号：T10214产 地：中国大陆
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T101907-BIA；化合物7-BIA7-BIA
7-BIA is a receptor-type protein tyrosine phosphatase D (PTPRD) inhibitor with anti-addictive properties and can be used in the study of neuropathic pain.
价 格：￥电议型 号：T10190产 地：中国大陆
