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19

抑制剂 & 化合物

2

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T0805	Quinapril hydrochloride CI-906,PD-109452-2,盐酸喹那普利,Quinapril HCl	RAAS	Endocrinology/Hormones
	Quinapril hydrochloride (PD-109452-2) 是一种血管紧张素转化酶(ACE) 抑制剂的原药。
T2486	IOWH-032 IOWH032,IOWH 032	CFTR; Autophagy	Autophagy; Membrane transporter/Ion channel
	IOWH-032 (IOWH032) 是一种合成 CFTR 抑制剂，可用于研究治疗霍乱、腹泻和分泌性腹泻，在T84和CHO-CFTR 细胞实验中IC50为1.01 uM。
T83602	(+)-Chloroquine
	(+)-Chloroquine是一种影响血管紧张素转换酶2（ACE-2）末端糖基化的氨基喹啉药物，其作用表现在体外。
T82500	Efmitermant alfa ACE083
	Efmitermant alfa (ACE-083)为一基于卵泡抑素的局部作用肌肉促进融合蛋白，主要应用于肌肉疾病研究领域。
T80099	Ovalbumin (154-159)	Angiotensin-converting Enzyme (ACE)	Metabolism
	Ovalbumin (154-159)为卵清蛋白片段，同时作为一种有效的血管紧张素转换酶 (ACE) 抑制剂，适用于高血压研究。
T70932	L6H9
	L6H9 is a novel inhibitor of myeloid differentiation factor 2 (MD2), suppressing HG-induced expression of ACE and AT1 receptor and Angiotensin II (AngII) production in renal NRK‐52E cells, resulting in the decrease in fibrosis markers such as TGF-β and collagen IV.
T73810	H-Ile-Pro-Pro-OH hydrochloride
	H-Ile-Pro-Pro-OH hydrochloride，一种源自乳制品的三肽，通过抑制血管紧张素转换酶 (ACE)，IC50为5 μM，展现出抗高血压效果。
T80100	Ovotransferrin (328-332)	Angiotensin-converting Enzyme (ACE)	Metabolism
	Ovotransferrin (328-332) 在控制血压方面具有保护效果，主要通过抑制血管紧张素转换酶 (ACE) 实现，其抗ACE活性的IC50为20μM。此外，Ovotransferrin (328-332) 片段还能够抑制乙酰胆碱酯酶 (ChE)，这是与阿尔茨海默病相关的特性。
T74109	Captopril EP Impurity B
	CaptoprilEPImpurity B 是一种 Captopril 的杂质。Captopril 是一种含巯基的口服活性血管紧张素转换酶(ACE)抑制剂 (IC50=0.025 μM)。
T77199	Methionylserine
	Methionylserine (H-MET-SER-OH) 是一种含有蛋氨酸和丝氨酸的二肽。Methionylserine 可与肠道二/三肽转运蛋白 1 (hPEPT1) 结合并易位，Km 值为 0.2 mM。Methionylserine 抑制ACE 酶的活性。Methionylserine 可用于高血压的研究。
T76613	H-Pro-Phe-OH
	H-Pro-Phe-OH 是一种含脯氨酸和苯丙氨酸的二肽，可作为脯氨酸酶的底物。H-Pro-Phe-OH 也能用于多肽的合成，其中苯丙氨酸是一种芳香族氨基酸，能抑制血管紧张素转换酶 (ACE) 的活性。
T21485	Perindopril
	Perindopril (S-9490) 是一种长效血管紧张素转换酶（ACE）抑制剂，用于治疗高血压、心力衰竭或稳定性冠状动脉疾病。
T37495	Angiotensin (1-7) (acetate)
	Angiotensin 1-7 (Ang-(1-7)) acetate 是RAS中的一种内源性七肽，具备心脏保护作用，主要表现为对心肌细胞的抗炎与抗纤维化活性。该化合物能抑制纯化的犬ACE活性（IC50=0.65 μM），通过降低ACE活性并促进一氧化氮释放，作为血管舒张调节的局部协同因子。此外，Angiotensin 1-7 acetate 可阻止血管紧张素Ⅱ诱发的平滑肌细胞增殖和肥大，同时对内皮细胞表现出抗血管生成和生长抑制作用。
T75752	N-Acetyl-Ser-Asp-Lys-Pro acetate
	N-Acetyl-Ser-Asp-Lys-Pro (Ac-SDKP) acetate 是血管紧张素转换酶 (ACE) N 端活性位点的特异性底物。N-Acetyl-Ser-Asp-Lys-Pro acetate 是多能干细胞增殖的天然抑制剂。N-Acetyl-Ser-Asp-Lys-Pro acetate 具有抗炎和抗纤维化特性。
T60383	Captopril hydrochloride
	Captopril (SQ 14225) hydrochloride 是一种含巯基的口服活性血管紧张素转换酶(ACE)抑制剂，IC50值为0.025 μM，已广泛应用于高血压和充血性心力衰竭的研究。Captopril hydrochloride 也是 NDM-1抑制剂，IC50值为 7.9 μM。
T35324	DX600
	DX600 是一种angiotensin-converting enzyme 2 (ACE2)的特异抑制剂，不会与ACE 发生交叉反应。
T68616	Pentoprilat
	Pentoprilat is a member of a series of l-glutarylindoline-2(S)-carboxylic acid derivatives. Pentopril was evaluated as an inhibitor of a cell-free preparation of angiotensin-converting enzyme (ACE) isolated from rabbit lung. Intravenous administration of incremental doses of pentopril to anesthetized normotensive rats produced a dose-related inhibition of angiotensin I (AI) pressor responses. The onset of inhibition of the A1 pressor response was rapid, and substantial inhibition occurred at 5 m...
T36622	Angiotensin I/II (1-6) (TFA)
	Angiotensin I/II (1-6) TFA is a chemical compound comprising amino acids 1-6. It is derived from the Angiotensin I/II peptide, which is formed by the cleavage of the precursor angiotensinogen by renin. The resulting Angiotensin I is then hydrolyzed by angiotensin-converting enzyme (ACE) to produce biologically active Angiotensin II. Angiotensin II has been extensively studied for its potential applications in the treatment of Hypertension, Renin Angiotensin System, and Idiopathic Membranous Neph...
T37496	Alamandine
	Alamandine can be formed from angiotensin A by action of ACE-2 or directly from angiotensin-(1-7) by decarboxylation of its aspartate residue. The angiotensin A analog produces effects resembling those of Ang II (1-7). However, it acts independently of the two known vasodilators receptors of the RAS (Mas and angiotensin II type 2). To produce its effects, alamandine binds to the Mas-related receptor, MrgD. A novel orally active formulation of alamandine produced a long-term antihypertensive effe...

化合物

Quinapril hydrochloride

Cat.No: T0805

Synonym: CI-906,PD-109452-2,盐酸喹那普利,Quinapril HCl

Target: RAAS

Cat.No: T2486

Synonym: IOWH032,IOWH 032

Target: CFTR, Autophagy

(+)-Chloroquine

Cat.No: T83602

Efmitermant alfa

Cat.No: T82500

Synonym: ACE083

Ovalbumin (154-159)

Cat.No: T80099

Target: Angiotensin-converting Enzyme (ACE)

Cat.No: T70932

H-Ile-Pro-Pro-OH hydrochloride

Cat.No: T73810

Ovotransferrin (328-332)

Cat.No: T80100

Target: Angiotensin-converting Enzyme (ACE)

Captopril EP Impurity B

Cat.No: T74109

Methionylserine

Cat.No: T77199

Cat.No: T76613

Cat.No: T21485

Angiotensin (1-7) (acetate)

Cat.No: T37495

N-Acetyl-Ser-Asp-Lys-Pro acetate

Cat.No: T75752

Captopril hydrochloride

Cat.No: T60383

Cat.No: T35324

Cat.No: T68616

Angiotensin I/II (1-6) (TFA)

Cat.No: T36622

Cat.No: T37496

Cat. No.	Product Name	Target	Signaling Pathways
T3851	Vicenin 2 Vicenin -2,维采宁 2,新西兰牡荆苷	RAAS	Endocrinology/Hormones
	Vicenin 2 来源于广金钱草 (Desmodium styracifolium) 的地上部分。Vicenin 2 是一种血管紧张素转换酶 (ACE) 抑制剂，IC50=43.83 μM。
TN4860	Pueroside B	COX; PPAR	DNA Damage/DNA Repair; Immunology/Inflammation; Metabolism; Neuroscience
	Pueroside B may can treat coronary heart disease, it can interact with two or more targets[peroxisome proliferator activated receptor γ (PPAR-γ), angiotensin-converting enzyme (ACE), hydroxymethylglutaryl coenzyme A receptor (HMGR), cyclooxygenase-2 (COX2

天然产物

Cat.No: T3851

Synonym: Vicenin -2,维采宁 2,新西兰牡荆苷

Target: RAAS

Cat.No: TN4860

Target: COX, PPAR

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