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T26530ABT-472；化合物 T26530A-620223 (HCl salt)|||AKOS016845980|||DTXSID70670431；A-620223 (HCl salt)|||AKOS016
ABT-472 is a novel PARP inhibitor
价 格：￥电议型 号：T26530产 地：中国大陆
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T25894NVP-AAD777；化合物 T25894AAD-777|||NVP-AAD-777|||NVP AAD 777；AAD-777|||NVP-AAD-777|||NVP AAD 777
NVP-AAD777 is a specific VEGFR-2 inhibitor.
价 格：￥电议型 号：T25894产 地：中国大陆
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T25824ML400；化合物ML400ML 400|||CID-73050863|||ML-400|||CID73050863|||CID 73050863；ML 400|||CID-73050863|||ML
ML400 (CID73050863) is an allosteric inhibitor of LMPTP with an EC50 of 1μM. ML400 displays good cell-based activity and rodent pharmacokinetics.
价 格：￥电议型 号：T25824产 地：中国大陆
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T25252Cimoxatone；化合物 T25252MD-780515|||MD780515|||MD 780515；MD-780515|||MD780515|||MD 780515
Cimoxatone is used as a Monoamine Oxidase Inhibitor.
价 格：￥电议型 号：T25252产 地：中国大陆
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T24721Robalzotan；化合物 T24721NAD-299|||AZD 7371|||AZD7371|||NAD 299|||AZD-7371；NAD-299|||AZD 7371|||AZD7371|
Robalzotan is a selective 5-HT1A receptor antagonist.
价 格：￥电议型 号：T24721产 地：中国大陆
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T2458CID755673；化合物CID755673CID755673
CID755673 is an effective and specific cell-active inhibitor for PKD (IC50: 182 nM); exhibits selective PKD1 inhibition when compared with PLK1, AKT, CAMKIIα, CAK, and PKC isoforms.
价 格：￥电议型 号：T2458产 地：中国大陆
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T23971DDD00079282；化合物 T23971DDD79282|||DDD-79282|||DDD-00079282|||DDD 00079282|||DDD 79282；DDD79282|||DDD-
DDD00079282 is an inhibitor of IMPDH.
价 格：￥电议型 号：T23971产 地：中国大陆
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T2353BRD7116；化合物BRD7716BRD7716；BRD7716
BRD7116 competitively binds to bacterial DNA gyrase, with cell-non-autonomous anti-leukemia activity.
价 格：￥电议型 号：T2353产 地：中国大陆
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T19273Debutyldronedarone D7；化合物 T19273SR-35021 D7；SR-35021 D7
Debutyldronedarone D7 is deuterium-labeled Debutyldronedarone, which is the main circulating active metabolite of dronedarone in the body.
价 格：￥电议型 号：T19273产 地：中国大陆
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T17697BRD7-IN-1；化合物BRD7-IN-1BRD7-IN-1
BRD7-IN-1, a modified derivative of BI7273 (BRD7/9 inhibitor), forms PROTAC VZ185 through linkage to a VHL ligand, demonstrating potent activity against BRD7/9 with DC50 values of 4.5 and 1.8 nM, respectively [1].
价 格：￥电议型 号：T17697产 地：中国大陆
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T17696BRD7-IN-1 free base；化合物 T17696BRD7-IN-1 free base
BRD7-IN-1 free base, a modified derivative of BI7273 (BRD7/9 inhibitor), interacts with a VHL ligand through a linker, constituting the PROTAC VZ185 (targeting BRD7/9 with DC50 values of 4.5 and 1.8 nM, respectively)[1].
价 格：￥电议型 号：T17696产 地：中国大陆
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T17033Temanogrel；化合物TemanogrelAPD791；APD791
Temanogrel (APD791) is a highly selective antagonist of the 5-HT2A receptor (Ki: 4.9 nM).
价 格：￥电议型 号：T17033产 地：中国大陆
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T15045D77；化合物 T15045D77
D77 is anti-HIV-1 inhibitor. D77 inhibits HIV-1(IIIB) replication by EC50 value of 23.8 μg/ml in MT-4 cell (5.03 μg/ml for C8166 cells).
价 格：￥电议型 号：T15045产 地：中国大陆
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T14779BRD7389；化合物BRD7389BRD7389
BRD7389 is an inhibitor of RSK family kinase with IC50s of 1.5 μM, 2.4 μM, and 1.2 μM for RSK1, RSK2, and RSK3, respectively.
价 格：￥电议型 号：T14779产 地：中国大陆
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T14382AZD7687；化合物 T14382AZD7687
AZD7687 is a potent and selective DGAT1 inhibitor with an IC50 value of 80 nM (hDGAT1). IC50 value: 80 nM [1] Target: DGAT1 in vitro: Plasma AZD7687 exposure was measured repeatedly. AZD7687 markedly reduced postprandial TAG excursion with a steep concentration-effect relationship [2]. Postprandial serum TAG excursion was measured during 8 h after a standardized mixed meal with fat energy content of 60% (SMM 60%; five cohorts, 1-20 mg), before (baseline) and after dosing, to assess effects on gu
价 格：￥电议型 号：T14382产 地：中国大陆
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T14381AZD7624；化合物AZD7624AZD-7624；AZD-7624
AZD7624 is an p38 inhibitor. It has potent anti-inflammatory activity.
价 格：￥电议型 号：T14381产 地：中国大陆
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T14380AZD7507；化合物CS-2850AZD7507
AZD7507 is a CSF-1R inhibitor with an IC50 of 32 nM. AZD7507 has antitumor activity.
价 格：￥电议型 号：T14380产 地：中国大陆
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T14313Apricitabine；阿立他滨AVX754|||SPD754；AVX754|||SPD754
Apricitabine (SPD754) is a highly selective and orally active HIV-1 reverse transcriptase inhibitor (Ki=0.08 μM), the (-) enantiomer of 2′-deoxy-3′-oxy-4′-thiocytidine (dOTC) . Apricitabine inhibits DNA polymerase α, β and γ with Ki values of 300 μM, 12 μM and 112.25 μM, respectively. Apricitabine has shown good antiretroviral therapeutic efficacy in antiretroviral HIV-infected patients, with good tolerability and low selective resistance.
价 格：￥电议型 号：T14313产 地：中国大陆
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T13181Tolcapone D7；化合物 T13181Ro 40-7592 D7；Ro 40-7592 D7
Tolcapone D7 is a deuterium-labeled Tolcapone. Tolcapone is a selective and orally active inhibitor of COMT.
价 格：￥电议型 号：T13181产 地：中国大陆
