clh

BAY-298 是一种口服有效且选择性的促黄体生成激素受体(LH-R)拮抗剂，分别针对hLH(人LH)、rLH(大鼠LH)和cLH(食蟹猴LH)展现出96 nM、23 nM和78 nM的IC50。作为一种纳摩尔级别的hLH-R拮抗剂，BAY-298 能够有效降低体内性激素水平。

(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(1H-imidazol-4-yl)propanoic acid 是一种组氨酸衍生物。

Boc-His-OH（Boc-组氨酸）是一种受保护的氨基酸衍生物，广泛用于肽合成和生物化学研究。N-Boc-L-Histidine在肽合成中作为中间体，用于构建多肽链，具有良好的化学稳定性和溶解性。

Capmatinib 2HCl.H2O (NVP-INC280 2HCl.H2O) 是一种具有潜在抗肿瘤活性的原癌基因 c-Met (HGFR) 的口服生物可利用抑制剂。

GSK3532795（亦称BMS-955176）是一种具有高效性的口服第二代HIV-1成熟抑制剂（MI），已进展至Ⅱb期临床试验。此化合物对多态病毒（EC50 <15 nM，涵盖代表96.5% HIV-1亚型B病毒的常见多态性）具有广泛的覆盖能力，并在临床前物种中展现了良好的药代动力学特性。

desensitising AMPA receptor agonist

DX-9065A is a factor Xa inhibitor. DX-9065a inhibits proinflammatory events induced by factor Xa and gingipains. DX-9065a is a competitive inhibitor of the Spectrozyme FXa (SpFXa) cleavage by both fXa and prothrombinase with similar K(i) values of approxi

BMS 433771 is an effective RSV replication inhibitor in vitro.

Trimetoquinol hydrochloride possesses differential and selective beta-adrenergic properties.

NH2-PEG5-C6-Cl hydrochloride is a polyethylene glycol (PEG)-based linker compound, commonly employed in the synthesis of proteolysis targeting chimeras (PROTACs).

NH2-PEG2-C6-Cl hydrochloride 是一种属于 PEG 类的 PROTAC 连接体，可用于合成 PROTAC 分子。

Talniflumate (Somalgen) 是一种钙激活氯离子通道 (hCLCA1 mCLCA3) 阻滞剂，可减少动物模型和细胞培养中的粘蛋白合成和释放。它通过抑制环氧合酶，并抑制 Cl- HCO3- 交换活性，具有抗炎作用。它还增加了远端肠梗阻综合征囊性纤维化小鼠模型的存活率。

Fmoc-L-HoLys(Boc)-OH 是一种有用的有机化合物，可用于生命科学领域的相关研究。其产品编号为 T65197，CAS号为 194718-17-7。

Fmoc-L-β-HoLeu-OH 是一种有用的有机化合物，可用于生命科学领域的相关研究。其产品编号为 T65828，CAS号为 193887-44-4。

Boc-L-Homoserine 是一种有用的有机化合物，可用于生命科学领域的相关研究。其产品编号为 T67363，CAS号为 41088-86-2。

Temiverine hydrochloride monohydrate is an anticholinergic drug with calcium antagonistic activity.

Zimeldine hydrochloride hydrate is a serotonin uptake inhibitor that was formerly used for depression but was withdrawn worldwide in September 1983 because of the risk of Guillain-Barre Syndrome associated with its use.

Y27632 is a selective ROCK inhibitor, which inhibits ET-1-induced increases in natriuretic peptide production, cell size, protein synthesis, and myofibrillar organization. Y27632 prevents dimethylnitrosamine-induced hepatic fibrosis in rats, increases apoptosis and disrupts the actin cortical mat in embryonic avian corneal epithelium, affects initial heart myofibrillogenesis in cultured chick blastoderm, promotes the proliferation and cell cycle progression of cultured astrocyte from spinal cord.

Dapivirine HCl is the salt form of Dapivirine, also known as TMC120, a non-nucleoside inhibitor for HIV reverse transcriptase with IC50 of 24 nM. The HIV-1 replication inhibitor dapivirine (DPV) is one of the most promising drug candidates being used in topical microbicide products for prevention of HIV-1 sexual transmission.

SB1-B-57 is an USP14 inhibitor.

Cgs 26303 is a potent non-peptidic inhibitor of neutral endopeptidase capable of protecting atrial natriuretic peptide from enzymatic degradation.

Filgotinib hydrochloride hydrate is a potent and selective JAK1 inhibitor under investigation for the treatment of rheumatoid arthritis (RA) and Crohn's disease.

KT172 是一种 DAGLβ抑制剂，IC50值为 11 nM。KT172 可用于代谢和炎症的研究。

Copanlisib Dihydrochloride is a novel phosphoinositide 3-kinase (pi3k) inhibitor, inhibiting the activation of the pi3k signaling pathway, resulting in inhibition of tumor cell growth and survival in susceptible tumor cell populations