tadalafil

Tadalafil (IC-351) 是一种PDE5抑制剂，IC50为 1.8 nM。

ent-Tadalafil (ent-IC-351), compound (6S,12aS), is a inactive cis-enantiomer of compound (6R,12aS).

N-Ethyl tadalafil (NEthyl tadalafil) 是一种 CGMP 特异性 3'，5'-环磷酸二酯酶（PDE）抑制剂，可用于研究心绞痛、高血压和肺动脉高压等心血管疾病。

cis-Tadalafil (cis-IC-351) 是一种有效的 PDE5 抑制剂 ，IC50 值为 0.09 μM，可用于研究动脉高压。

Tadalafil hydroxypiperidone is an impurity of Tadalafil -- a phosphodiesterase 5-inhibitor used for the treatment of erectile dysfunction.

Desmethylene Tadalafil is a phosphodiesterase 5 inhibitor.

Tadalafil-d3 是 Tadalafil 的氘代化合物。Tadalafil 的 CAS 号为 171596-29-5。Tadalafil 是一种PDE5抑制剂，IC50为 1.8 nM。

Nortadalafil (Demethyl Tadalafil) 是 demethyl Tadalafil，是一种 PDE5 抑制剂。

Amino Tadalafil 是一种 Tadalafil 的类似物，是一种磷酸二酯酶 5 抑制剂，可用于多种疾病，如勃起功能障碍，肺动脉高压和下尿路功能障碍。

cis-ent-Tadalafil (cis-ent-IC-351) 是一种具有高效和选择性的 PDE5 抑制剂，可降低血压。

Tadalafil-13C-d3 是 Tadalafil 的 13C 和氘代化合物。Tadalafil 的 CAS 号为 171596-29-5。Tadalafil 是一种PDE5抑制剂，IC50为 1.8 nM。

Apricoxib, also known as Benzenesulfonamide 42(4ethoxyphenyl)4methyl1Hpyrrol1yl, is an orally bioavailable nonsteroidal anti-inflammatory agent (NSAID) with potential antiangiogenic and antineoplastic activities. Apricoxib binds to and inhibits the enzyme cyclooxygenase-2 (COX-2), thereby inhibiting the conversion of arachidonic acid into prostaglandins. Apricoxib-mediated inhibition of COX-2 may induce tumor cell apoptosis and inhibit tumor cell proliferation and tumor angiogenesis. COX-related metabolic pathways may represent crucial regulators of cellular proliferation and angiogenesis.

Acetaminotadalafil is a new analogue of Tadalafil used for the treatment of erectile dysfunction. It acts as a phosphodiesterase 5 inhibitor.

Acetaminotadalafil (Standard) is the standard substance of Acetaminotadalafil, and it is applicable for quantitative analysis, quality control, and related research in biochemical experiments. Acetaminotadalafil is a new analogue of Tadalafil used for the treatment of erectile dysfunction. It acts as a phosphodiesterase 5 inhibitor.