关于 "Reverse Transcriptase" 的结果13 个结果

Censavudine (OBP-601; BMS-986001)，一种核苷类似物，是一种核苷逆转录酶 (nucleoside reverse transcriptase) 抑制剂。Censavudine 是一种有效的 HIV 抑制剂，对 HIV-2 和 HIV-1 的 EC50 范围分别为 30-81 nM 和 450-890 nM。

Foscarnet sodium (Trisodium phosphonoformate) 是一种病毒 DNA 聚合酶活性抑制剂，可导致病毒复制的可逆抑制。

Zidovudine是一种合成核苷类似物，通过抑制逆转录酶阻断人类免疫缺陷病毒（HIV）的复制。

阿巴卡韦是一种具有口服活性和竞争性的核苷类逆转录酶抑制剂。

A reversible inhibitor of CK1

2',3'-Dideoxyadenosine 5'-triphosphate (2',3'-Dideoxyadenosine 5'-triphosphate), an active metabolite of 2',3'-dideoxyinosine, is a chain-elongating inhibitor of DNA polymerase.

4'-Methoxychalcone, found in citrus, is chalcone derivative that has shown diverse pharmacological properties, including anti-tumor and anti-inflammatory activities. 4'-Methoxychalcone significantly enhanced adipocyte differentiation, in part, by its potent effects on PPARγ activation and by its reverse effect on TNF-α.

Trilaciclib (G1T28, G1T28-1) is a highly potent, selective and reversible cyclin-dependent kinase 4 and 6 (CDK4/6) inhibitor. Trilaciclib inhibits CDK4/cyclin D1 and CDK6/cyclin D3 with IC50 of 1 nM and 4 nM, respectively.

A-3 hydrochloride, a potent, cell-permeable, reversible, ATP-competitive non-selective antagonist of various kinases, againsts cAMP-dependent protein kinase (PKA) (Ki=4.3 ?M), casein kinase II (CK2) (Ki=5.1 ?M) and myosin light chain kinase (MLCK) (Ki=7.4 ?M), also inhibits Protein Kinase C (PKC) and casein kinase I (CK1) with Ki values of 47 ?M and 80 ?M, respectively.

An ATM kinase inhibitor

LDN 57444是一种小分子抑制剂，可阻断UCHL1的去泛素化酶活性（K i =0.40μM；IC 50 =0.88μM），抑制UCHL3的IC 50 值为25μM。

阿非迪霉素是真核DNA复制的可逆抑制剂，可阻断前S期的细胞周期。

Brefeldin A（BFA）是一种真菌大环内酯，能够有效、可逆地抑制内质网和高尔基体之间的蛋白质运输和囊泡形成。