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T0805Quinapril hydrochloridePD-109452-2；Quinapril HCl；CI-906；盐酸喹那普利
Quinapril is an angiotensin-converting enzyme (ACE) inhibitor used in the therapy of hypertension and congestive heart failure. Quinapril is associated with a low rate of transient serum aminotransferase elevations, but has yet to be linked to instances o
价 格：￥电议型 号：T0805产 地：中国大陆
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T0682Lamivudine拉米夫定；GR109714X；BCH-189
Lamivudine is a reverse transcriptase inhibitor and ZALCITABINE analog in which a sulfur atom replaces the 3´ carbon of the pentose ring. It is used to treat HIV disease.
价 格：￥电议型 号：T0682产 地：中国大陆
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T0120Voriconazole伏立康唑；UK-109496
Voriconazole is a triazole antifungal agent that specifically inhibits STEROL 14-ALPHA-DEMETHYLASE and CYTOCHROME P-450 CYP3A.
价 格：￥电议型 号：T0120产 地：中国大陆
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T0115Idazoxan hydrochloride盐酸咪唑克生；RX 781094
Idazoxan hydrochloride is a benzodioxane-linked imidazole. It has alpha-2 adrenoceptor antagonist activity.
价 格：￥电议型 号：T0115产 地：中国大陆
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T0109Molsidomine吗多明；Morsydomine；SIN-10；Corvaton
Molsidomine is an orally active, long-acting vasodilating drug. It metabolizes in the liver to the active metabolite linsidomine, that releases nitric oxide (NO) upon decay as the actual vasodilating compound.
价 格：￥电议型 号：T0109产 地：中国大陆
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T0109MolsidomineMolsidomine,Morsydomine,SIN-10
Molsidomine is an orally active, long-acting vasodilating drug. It metabolizes in the liver to the active metabolite linsidomine, that releases nitric oxide (NO) upon decay as the actual vasodilating compound.
价 格：￥电议型 号：T0109产 地：美洲
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T0115Idazoxan hydrochlorideIdazoxan hydrochloride,RX 781094,
Idazoxan hydrochloride is a benzodioxane-linked imidazole. It has alpha-2 adrenoceptor antagonist activity.
价 格：￥电议型 号：T0115产 地：美洲
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T0120VoriconazoleVoriconazole,UK-109496,
Voriconazole is a triazole antifungal agent that specifically inhibits STEROL 14-ALPHA-DEMETHYLASE and CYTOCHROME P-450 CYP3A.
价 格：￥电议型 号：T0120产 地：美洲
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T0682LamivudineLamivudine,BCH-189,GR109714X
Lamivudine is a reverse transcriptase inhibitor and ZALCITABINE analog in which a sulfur atom replaces the 3´ carbon of the pentose ring. It is used to treat HIV disease.
价 格：￥电议型 号：T0682产 地：美洲
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T10480Bay 41-4109 (less active enantiomer)Bay 41-4109 (less active enantiomer)
Bay 41-4109 less active enantiomer shows less activity than Bay 41-4109. BAY 41-4109 is a potent HBV inhibitor (IC50: 53 nM).
价 格：￥电议型 号：T10480产 地：美洲
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T10480LBay 41-4109Bay 41-4109
BAY 41-4109 is a potent inhibitor of human hepatitis B virus (HBV)(IC50 : 53 nM).
价 格：￥电议型 号：T10480L产 地：美洲
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T1055IfosfamideIfosfamide,NSC109724,Isophosphamide
Ifosfamide alkylates and forms DNA crosslinks, thereby preventing DNA strand separation and DNA replication. Ifosfamide is a synthetic analog of the nitrogen mustard cyclophosphamide with antineoplastic activity. This agent is a prodrug that must be activ
价 格：￥电议型 号：T1055产 地：美洲
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T10566BMS-191095BMS-191095
BMS-191095 is mitochondrial ATP-sensitive potassium (mitoKATP) channel activator.
价 格：￥电议型 号：T10566产 地：美洲
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T1091ChlortalidoneChlortalidone,Chlorthalidone,
Chlorthalidone is a benzenesulfonamide-phthalimidine that tautomerizes to a BENZOPHENONES form. It is considered a thiazide-like diuretic.
价 格：￥电议型 号：T1091产 地：美洲
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T1092ZolmitriptanZolmitriptan,BW-311C90,311C90
Zolmitriptan selectively binds to and activates serotonin (5-HT) 1B receptors expressed in intracranial arteries and 5-HT 1D receptors located on peripheral trigeminal sensory nerve terminals in the meninges and central terminals in brainstem sensory nucl
价 格：￥电议型 号：T1092产 地：美洲
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T10920Cyclo(Arg-Gly-Asp-D-Phe-Val) TFACyclo(Arg-Gly-Asp-D-Phe-Val) TFA
Arg-Gly-Asp-D-Phe-Val (TFA) has anti-tumor activity and is an inhibitor of integrin αvβ3.
价 格：￥电议型 号：T10920产 地：美洲
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T10921CYM 9484CYM 9484
CYM 9484 is a selective and potent neuropeptide Y (NPY) Y2 receptor antagonist with IC50 value of 19 nM.
价 格：￥电议型 号：T10921产 地：美洲
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T10925Cysteine Protease inhibitorCysteine Protease inhibitor
Cysteine protease inhibitors are inhibitors of cysteine proteases. Target: Cysteine Protease
价 格：￥电议型 号：T10925产 地：美洲
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T10926CYT-1010CYT-1010
CYT-1010 is an mu-opioid receptor agonist extracted from patent WO2013173730A2. The EC50 for the inhibition of β-arrestin recruitment and cAMP production is 13.1 nM and 0.0053 nM, respectively.
价 格：￥电议型 号：T10926产 地：美洲
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T10929LD-3263 hydrochlorideD-3263 hydrochloride
D-3263 hydrochloride is enteric-coated, orally bioavailable (transient receptor potential melatonin member 8) TRPM8 agonist.
价 格：￥电议型 号：T10929L产 地：美洲
