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货号 产品名 纯度
A570430 现货 5,7-Diacetoxy-8-methoxyflavone

5,7-Diacetoxy-8-methoxyflavone is a natural product isolated and purified from the roots of Scutellaria baicalensis.

98%+
A1216753 现货 Lirimilast

Lirimilast是一种有效且选择性的口服磷酸二酯酶 4 (PDE4) 抑制剂,IC50 为 49 nM,主要用于研究哮喘和慢性阻塞性肺疾病 (COPD),具有显著的抗炎活性【183】。

98%
A111758 现货 N-Methylbenzamide/N-甲基苯甲酰胺

N-Methylbenzamide is a potent phosphodiesterase 10A (PDE10A) inhibitor. N-Methylbenzamide has anti-cancer activity.

97%
A982733 现货 (E/Z)-Ensifentrine

Ensifentrine is an inhaled first-in-class dual inhibitor of phosphodiesterase 3 (PDE3) and PDE4 with IC50s of 0.4 nM and 1479 nM, respectively.

99%+
A304814 现货 MY-5445

MY-5445 is a specific inhibitor of cyclic GMP phosphodiesterase 5 with IC50 of 0.5 μM.

98%
A1327292 现货 DSR-141562

DSR-141562 is a novel orally available and brain-penetrant PDE 1 inhibitor. It has preferential selectivity for predominantly brain-expressed PDE1B over other PDE1 family members, and high selectivity for the PDE1 family over other PDE families and 65 other tested biologic targets.

99%+
A726292 现货 ITI-214

ITI-214 is a picomolar PDE1 inhibitor with excellent selectivity against other PDE family members and against a panel of enzymes, receptors, transporters, and ion channels, exhibits potent PDE1 inhibitory activity (Ki = 58 pM).

99%+
A859609 现货 OR-1896

OR-1896 是 Levosimendan 的活性代谢产物,作为一种高选择性的磷酸二酯酶 (PDE III) 抑制剂,同时是一种强效血管扩张剂,能够打开 ATP 敏感的 K+ 通道,并具有钙敏感作用,可减轻心肌细胞凋亡、心脏重塑和心肌炎症。

98+%
A985435 现货 (S)-C33

(S)-C33 is a potent PDE9 inhibitor with IC50 of 11 nM.

99%+
A723969 现货 CP671305

CP-671,305 is a potent and selective PDE4D inhibitor.

99%+
A122751 现货 ICI-63197

ICI 63197 is a potent phosphodiesterase (PDE) 4 inhibitor with antidepressant effects.

95%
A860292 现货 3-O-Methylquercetin/3-O-甲基槲皮素

3-O-Methylquercetin, a natural product isolated and purified from the herbs of Croton cascarilloides with antiviral, anti-inflammatory and bronchodilating effects, is a selective and competitive PDE3/PDE4 inhibitor, and inhibits PDE3 than PDE4 with a low K(m) value. 3-O-Methylquercetin also inhibits total cAMP- and cGMP-phosphodiesterase (PDE) of guinea pig trachealis at low concentrations.

98%
A1537879 现货 FEN1-IN-SC13

SC13 specifically inhibits FEN1 activity. It suppresses cancer cell proliferation and induces chromosome instability and cytotoxicity in cells, as well as sensitizes cancer cells to DNA damage-inducing therapeutic modalities and impedes cancer progression in a mouse model.

99%+
A122816 现货 Edelinontrine

PF-04447943 is a potent, selective brain penetrant PDE9 inhibitor (Ki of 2.8, 4.5 and 18 nM) for human, rhesus and rat recombinant PDE9 respectively and high selectivity for PDE9 versus PDEs1-8 and 10-11.

98%
A1177318 现货 NSP-805

NSP-805是一种高效、选择性的磷酸二酯酶 3 (PDE3) 抑制剂,具有强心和血管扩张作用,适用于心血管疾病的研究,特别是在治疗心力衰竭和血液循环不良方面有广泛应用。

99%+
A1217781 现货 PDE5-IN-9

PDE5-IN-9是一种 PDE5 抑制剂 (IC50: 11.2 μM),与 Gln 817、Tyr 612 和 Ala 767 氨基酸残基相互作用,可用于心血管疾病的研究。

99%+
A1251838 现货 HA155

HA155是一种高效、选择性的 ATX (自噬酰基转移酶) 抑制剂,其 IC50 为 5.7 nM,适用于肿瘤和纤维化等疾病的研究,尤其是在涉及 ATX 信号通路时具有重要的治疗潜力。

98%
A1280080 现货 Dasantafil

Dasantafil是一种小分子磷酸二酯酶 5A (PDE5A) 抑制剂,主要用于研究泌尿生殖系统疾病,特别是勃起功能障碍的治疗。

98%
A1340223 现货 (E/Z)-HA155

(E/Z)-HA155是一种强效的自分泌运动因子 autotaxin (ATX) I 型抑制剂,能够抑制 ATX-LPA 信号通路,具有研究癌症、纤维化、炎症和疼痛的潜力。

98%
A1445357 现货 PF-00489791

PF-00489791是一种选择性磷酸二酯酶 5A (PDE5A) 抑制剂,IC50 为 1.5 nM,能够通过增强肾脏血管的松弛来降低血压并改善肾功能,特别适用于高血压和糖尿病肾病的治疗研究。

99%+
产品名 PDE PDE1 PDE10A PDE2 PDE3 PDE4 PDE5 PDE6 其他靶点 纯度
Doxofylline 99+%
Deltarasin +++

PDEδ , Kd: 38 nM

99+%
7-(2,3-Dihydroxypropyl)theophylline 98%
Aminophylline +

PDE, IC50: 0.12 mM

98+%
Anagrelide HCl 99%+
Irsogladine AChR,mAChR 98%
PF-8380 +++

Autotaxin, IC50: 2.8 nM

99%+
Dipyridamole 98%
Balipodect ++++

PDE10A, IC50: 0.3 nM

99%+
PF-2545920 ++++

PDE10A, IC50: 0.37 nM

97%
Luteolin +

PDE1, Ki: 15.0 μM

++

PDE2, Ki: 6.4 μM

+

PDE3, Ki: 13.9 μM

+

PDE4, Ki: 11.1 μM

+

PDE5, Ki: 9.5 μM

98%
Milrinone ++

PDE2, IC50: 5.2 μM

++

PDE3, IC50: 2.1 μM

ATPase 98%
Pimobendan ++

PDE3, IC50: 0.32 μM

98%
Cilostazol ++

PDE3, IC50: 0.2 μM

98%
Fenspiride HCl +

PDE3, pIC50: 3.44

+

PDE4, pIC50: 4.16

98%
(S)-(+)-Rolipram ++

PDE4, IC50: 0.75 μM

98%
Apremilast +++

PDE4, IC50: 74 nM

98%
GSK256066 ++++

PDE4B, IC50: 3.2 pM

98+%
Roflumilast ++++

PDE4A4, IC50: 4.3 nM

PDE4A1, IC50: 0.7 nM

99%
Rolipram +++

PDE4B, IC50: 130 nM

99%+
Cilomilast +++

HPDE4, IC50: 120 nM

LPDE4, IC50: 100 nM

98+%
Avanafil ++++

PDE5, IC50: 1 nM

98%
Vardenafil HCl Trihydrate ++++

PDE5, IC50: 0.7 nM

98%
Tadalafil ++++

PDE5, IC50: 1.8 nM

98%
Icariin ++

PDE5, IC50: 0.432 μM

98%
Sildenafil +++

PDE6, IC50: 33 nM

98%
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。
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