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Search Results for " angiotensin i "

46

抑制剂 & 化合物

4

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
TP1528	Angiotensin I/II (1-5) Angiotensin I/II 1-5	RAAS; Others	Endocrinology/Hormones; Others
	Angiotensin I/II (1-5) 是由血管紧张素 I/II 肽转化而来，有 1-5 个氨基酸组成的多肽。血管紧张素 I 是由肾素对血管紧张素原的作用形成的，血管紧张素 I 可产生血管紧张素 II 。血管紧张素 II 用于高血压、特发性膜性肾病和肾素-血管紧张素系统的研究。
TP1579	Angiotensin I/II (1-6) Angiotensin I/II 1-6	RAAS; Others	Endocrinology/Hormones; Others
	Angiotensin I/II (1-6) 是由血管紧张素 I/II 肽转化而来，含有 1-6 个氨基酸的多肽。血管紧张素 I 被血管紧张素转换酶水解，形成具有生物活性的血管紧张素 II。血管紧张素 II 用于高血压、特发性膜性肾病和肾素-血管紧张素系统的研究。
TP1295	Angiotensin I (human, mouse, rat) Angiotensin 1 Human,血管紧张素 1 (人)	Others	Others
	Angiotensin I (human, mouse, rat) 是血管紧张素Ⅱ的前体物质，在血管紧张素转化酶 (ACE) 的参与下裂解成血管紧张素Ⅱ。
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...
TP2447	Angiotensin I, asn(1)-val(5)-gly(9)-
	Angiotensin I, asn(1)-val(5)-gly(9)- is isolated from the plasma of American eel, Anquilla rostrata.
T7714	Temocapil	Tyrosinase	Proteases/Proteasome
	Temocapil 是一种酪氨酸激酶抑制剂。
T6340	Enalaprilat Dihydrate 依那普利拉二水合物,MK-422,MK-422 Dihydrate	RAAS; Autophagy	Autophagy; Endocrinology/Hormones
	Enalaprilat Dihydrate (MK-422 Dihydrate) 是一种有效的血管紧张素转化酶抑制剂，IC50为 1.94 nM。
T6698	Temocapril hydrochloride CS-622 HCl,Acecol,Temocapril HCl,CS-622,盐酸替莫普利	RAAS	Endocrinology/Hormones
	Temocapril hydrochloride (CS-622 HCl) 是血管紧张素转化酶 (ACE) 抑制剂。Temocapril HCl 能够用于充血性心力衰竭、急性心肌梗死、高血压、胰岛素抵抗和肾脏疾病的研究。
T19930	Nitrosoglutathione S-Nitrosoglutathione,S-亚硝基谷胱甘肽,SNOG,Glutathione thionitrite,GSNO	RAAS; NO Synthase	Endocrinology/Hormones; Immunology/Inflammation
	Nitrosoglutathione (GSNO) 是一种外源性的 NO 供体，是大鼠酒精脱氢酶III 类同工酶的底物，能够减少脑血管紧张素II 依赖性及非依赖型的 AT1 受体反应。
T7663L	Angiotensin 1/2 (1-9) TFA(34273-12-6(free base))	Others	Others
	Angiotensin 1/2 (1-9) TFA(34273-12-6(free base)) 含有从血管紧张素 I/II 肽转化而来的氨基酸 1-9。
T3281	Delapril hydrochloride indalapril,地拉普利盐酸盐,Alindapril Hydrochloride,Delapril Hydrochloride,盐酸地拉普利,CV 3317	RAAS	Endocrinology/Hormones
	Delapril hydrochloride (indalapril) 是一种血管紧张素转化酶抑制剂，能够用于心血管疾病的研究。
T1484L	Perindopril erbumine 培哚普利叔丁胺,培哚普利叔丁胺盐,S9490-3,Perindopril tert-butylamine salt	Apoptosis; RAAS; MRP	Apoptosis; Endocrinology/Hormones; Immunology/Inflammation
	Perindopril erbumine (S9490-3) 是一种长效血管紧张素转换酶抑制剂。
T0215	Losartan potassium DuP-753 potassium,洛沙坦钾,氯沙坦钾,MK 954,DuP 753	RAAS	Endocrinology/Hormones
	Losartan potassium (DuP-753 potassium) 是一种血管紧张素 II 受体 1 型(AT1)拮抗剂，能够与血管紧张素 II 与 AT1 的结合竞争,其 IC50=20 nM。
T7354	H-Val-Pro-Pro-OH	RAAS	Endocrinology/Hormones
	H-Val-Pro-Pro-OH 是一种血管紧张素 I 转化酶(ACE)的抑制剂(IC50:9 μM)。他是一种来源于牛奶的脯氨酸肽衍生物。
T5964	Olmesartan CS 088,奥美沙坦,RNH 6270	RAAS	Endocrinology/Hormones
	Olmesartan (RNH 6270) 是一种血管紧张素 II 受体 (AT1R) 拮抗剂，常用于研究高血压。
TP1682L	Abz-FR-K(Dnp)-P-OH acetate(500799-61-1 free base)	Others	Others
	Abz-FR-K(Dnp)-P-OH acetate(500799-61-1 free base) 是一种出色的血管紧张素 I 转换酶 (ACE) 底物，Km 值为 4.0 μM，kcat 值为 210s-1。
T1462	Captopril SQ 14225,甲巯丙脯酸,卡托普利,SQ-14534,SA333	RAAS	Endocrinology/Hormones
	Captopril (SA333) 是一种含巯基的，具有口服活性的血管紧张素转换酶(ACE)抑制剂，IC50=0.025 μM，广泛应用于高血压和充血性心力衰竭的研究。Captopril 也是NDM-1抑制剂，IC50=7.9 μM。
T25515	I5B2 I5 B2,I5-B2
	I5B2 is a novel phosphorus-containing angiotensin I converting enzyme inhibitor. Angiotensin I converting enzyme is produced by Actinomadura sp.
T3281L	Delapril Alindapril
	Delapril is an ACE inhibitor. It blocks the conversion of angiotensin I to angiotensin II.
T25094	Antibiotic K 4 I5B1,I5 B1,K-4,K4,I5-B1
	Antibiotic K 4 is an inhibitor of angiotensin I converting enzyme produced by Actinomadura spiculosospora.
T1615L	Irbesartan HCl Irbesartan hydrochloride,BMS186295,BMS 186295,BMS-186295
	Irbesartan is an angiotensin II receptor antagonist used mainly for the treatment of hypertension. It selectively and competitively blocks the binding of angiotensin II to the angiotensin I receptor.
T29702	AG 85-12 AG-85-12,AG85-12
	AG 85-12 is a mimic of the C-terminal portion of angiotensin I.
T7663	Angiotensin 1/2 (1-9)	Others	Others
	Angiotensin 1/2 (1-9) 含有从血管紧张素 I/II 肽转化而来的氨基酸 1-9。
T76169	Angiotensin-converting enzyme
	Angiotensin-converting enzyme (ACE)血管紧张素转换酶是一种二羧基肽酶，它将非活性的血管紧张素 I (Ang I) 转化为活性的 Ang II，并降解活性的缓激肽 (BK)。Angiotensin-converting enzyme 是一种有效的血管收缩剂，常用于生化研究。
T22575	Angiotensin Fragment 1-7 (acetate)	Others	Others
	Angiotensin Fragment 1-7 is a type 1 angiotensin II receptor agonist. In the renin-angiotensin system, angiotensin I is cleaved by the angiotensin-converting enzyme to form angiotensin II, which has effects on fluid and electrolyte, as well as homeostasis
T22572	Angiotensin 1/2 (1-7) amide	Others	Others
	Angiotensin I/II (1-7) amide is a peptide analog to angiotensin II that is used as a vasopressor in the treatment of certain types of shock and circulatory collapse. Angiotensin I/II amide is an amide derivative of angiotensin II that is a powerful vasoco
T28632	RXP-407 RXP407
	RXP 407 is a selective inhibitor of the N-domain of angiotensin I-converting enzyme. RXP 407 blocks the degradation of hemoregulatory peptide acetyl-Ser-Asp-Lys-Pro with no effect on angiotensin I hydrolysis in vivo.
T22573	Angiotensin 1/2 (2-7)	Others	Others
	Angiotensin I/II (2-7) is a peptide that contains the amino acids 2-7 and is converted from Angiotensin I/II peptide. Angiotensin is a peptide hormone that causes vasoconstriction and a subsequent increase in blood pressure. Angiotensin also stimulates th
T25238	Chlorambucyl-proline
	Chlorambucyl-proline is a chlorambucil derivative of L-proline. It is an inhibitor of bovine lung angiotensin I-converting enzyme.
T71787	Deserpidine hydrochloride
	Deserpidine hydrochloride is the salf form of Deserpidine (free base), which is an antihypertensive drug related to reserpine which occurs naturally in Rauwolfia canescens. Deserpidine is a competitive inhibitor of the angiotensin converting enzyme (ACE). By competing with angiotensin I for ACE, deserpidine blocks the conversion of angiotensin I to angiotensin II, which is a potent vasoconstrictor. Reduced level of serum angiotensin II causes a decrease in blood pressure. Deserpidine also decrea...
TP1842	Angiotensinogen (1-14), human
	Angiotensinogen is a serum globulin formed by the liver that is cleaved by renin to form angiotensin I. Angiotensinogen is also called angiotensin precursor.
T19631	PD 109488 PD-109488,Quinapril Diketopiperazine,PD109488
	PD 109488 is a metabolite of quinapril and is a derivative of Quinapril that acts as an ACE inhibitor. Inhibition of ACE prevents the conversion of signaling peptide angiotensin I into angiotensin II, which acts as a potent vasoconstrictor. Reduced levels of angiotensin II also reduces the amount of aldosterone that is expressed due to RAAS signaling.
TP1682	Abz-FR-K(Dnp)-P-OH
	Excellent angiotensin I-converting enzyme (ACE) substrate with a Km value of 4.0 μM and a kcat value of 210s-1.
T72318	Trandolaprilate hydrate Trandolaprilat hydrate ; RU 44403 hydrate,RU 44403 hydrate,Trandolaprilat hydrate
	Trandolaprilate hydrate 是一种有效的血管紧张素转换酶 (ACE) 抑制剂。Trandolaprilate hydrate 可部分抑制血管紧张素 I 介导的c-fos 诱导。Trandolaprilate hydrate 是 Trandolapril 的主要生物活性代谢物。Trandolaprilate hydrate 具有较高的亲脂性。
T62005	Imidapril
	Imidapril (TA-6366 free base) 是口服有效的血管紧张素转换酶（ACE）和MMP-9抑制剂。Imidapril 通过抑制血管紧张素 I 向血管紧张素 II 转化从而降低总外周阻力和血压。Imidapril 在高血压、1 型糖尿病、肾病和慢性心力衰竭中有研究价值。
T76246	NH2-AKK-COOH
	NH2-AKK-COOH，一种合成三肽，是 ACE 抑制剂，当 FAPGG，HHL 和血管紧张素-I 用作底物时的 IC50值分别为 0.090 μM，0.178 μM 和 420.89 μM。
T68435	Cilazapril HCl
	Cilazapril, also known as Ro 31 2848, is a potent ACE inhibitor used for hypertension. Cilazapril is a prodrug that is hydrolyzed after absorption to its main metabolite cilazaprilat. Cilazapril is a monoethyl ester, which acts as an angiotensin-converting enzyme (ACE) inhibitor. The inhibitor functions by inhibiting the ability of ACE to cleave bonds of angiotensin I and Hip-His-Leu. It is known that the diacid form of Cilazapril is more potent that enalapril at inhibiting ACE.
T76610	Hippuryl-His-Leu-OH
	Hippuryl-His-Leu-OH 是一种血管紧张素 I 转换酶的活性检测底物。Hippuryl-His-Leu-OH 释放的 His-Leu 能与邻苯二甲醛或荧光胺 (Fluorescamine) 反应，用于荧光检测。
T71065	Quinapril-d5
	Quinapril-d5 is intended for use as an internal standard for the quantification of quinapril by GC- or LC-MS. Quinapril is a prodrug form of the angiotensin converting enzyme (ACE) inhibitor quinaprilat. In vivo, quinapril reduces mean arterial pressure in renal hypertensive and spontaneously hypertensive rats. It inhibits angiotensin I-induced pressor responses in normotensive rats and dogs. Quinapril prevents left ventricular heart failure in CHF 14.6 cardiomyopathic hamsters. Formulations con...
T75733	Saralasin TFA
	Saralasin ([Sar1,Ala8] Angiotensin II) TFA，血管紧张素 II (angiotensin II) 的八肽衍生物，作为竞争性血管紧张素 II 受体 (angiotensin II receptor) 拮抗剂，其Ki值达0.32 nM（涵盖74%的结合位点），显示出部分激动剂特性。适应于肾血管性高血压、肾素依赖性（血管紧张素原性）高血压的研究。
T62297	H-Val-Pro-Pro-OH TFA
	H-Val-Pro-Pro-OH (TFA) 是一种血管紧张素 I 转化酶(ACE)的抑制剂 (IC50: 9 μM)。H-Val-Pro-Pro-OH (TFA) 是一种来源于牛奶的脯氨酸肽衍生物。
T71205	Fosinopril-d7 sodium salt
	Fosinopril-d7 is intended for use as an internal standard for the quantification of fosinopril by GC- or LC-MS. Fosinopril is a prodrug form of the angiotensin-converting enzyme inhibitor fosinoprilat. Oral administration of fosinopril inhibits angiotensin I-induced pressor responses in normotensive rats, dogs, and monkeys when administered at doses of 15, 15, and 10 µmol/kg, respectively. Fosinopril reduces fractional shortening and decreases left ventricular size in a porcine model of congesti...
T74142	Angiotensin II human TFA
	Angiotensin II human (Angiotensin II) TFA 作为肾素/血管紧张素系统中关键的生物活性肽，扮演着血管收缩剂的角色并在调节人体血压中发挥中心作用。其主要通过与 G 蛋白偶联受体 (GPCRs)、血管紧张素 II 1型受体 (AT1R) 和血管紧张素 II 2型受体 (AT2R) 的相互作用来介导效应，包括刺激交感神经系统、增加醛固酮的生物合成和肾脏功能。此外，Angiotensin II human TFA 促进血管平滑肌细胞的生长和 I 型及 III 型胶原在成纤维细胞中的合成，导致血管壁与心肌增厚及纤维化，并诱导细胞凋亡。还通过LOX-1依赖的氧化还原敏感路径诱导内皮细胞中的毛细血管形成。
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...
T63425	Spirapril hydrochloride
	Spirapril (SCH 33844) hydrochloride 是血管紧张素转换酶 (ACE) 的有效抑制剂，是一种口服具有活力的螺普利拉前药。Spirapril hydrochloride 能够竞争性地与 ACE 结合，阻断血管紧张素I 向血管紧张素 II 的转化，表现出降压活性。Spirapril hydrochloride 能够用于研究高血压、充血性心力衰竭。
T83768	Zofenoprilat Zofenopril-SH,SQ 26,333
	Zofenoprilat是一种血管紧张素转换酶(ACE; IC50 = 8 nM for the rabbit lung enzyme)的抑制剂，同时也是前体药zofenopril的活性代谢产物。它能够抑制分离的豚鼠小肠中由血管紧张素I或缓激肽诱导的收缩(EC50s = 3 and 1 nM, respectively)。在人类脐静脉内皮细胞(HUVECs)中，Zofenoprilat (10 nM)降低基础内皮素-1分泌和一氧化氮(NO)生成，并阻止TNF-α诱导的活性氧种(ROS)增加以及谷胱甘肽(GSH)水平降低。Zofenoprilat (10 µM)保护初级人类心脏微血管内皮细胞免受多柔比星诱导的细胞毒性。此外，Zofenoprilat (10 µM)还能增加HUVECs中的硫化氢(H2S)生成，以及细胞的黏着、迁移和增殖。在以400 µM浓度使用时，它可以减少Langendorff分离的大鼠心脏灌流缺血再灌注损伤模型中的舒张末压和乳酸脱氢酶(LDH)释放。

化合物

Angiotensin I/II (1-5)

Cat.No: TP1528

Synonym: Angiotensin I/II 1-5

Target: RAAS, Others

Angiotensin I/II (1-6)

Cat.No: TP1579

Synonym: Angiotensin I/II 1-6

Target: RAAS, Others

Angiotensin I (human, mouse, rat)

Cat.No: TP1295

Synonym: Angiotensin 1 Human,血管紧张素 1 (人)

Target: Others

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

Cat.No: T36622

Angiotensin I, asn(1)-val(5)-gly(9)-

Cat.No: TP2447

Cat.No: T7714

Target: Tyrosinase

Enalaprilat Dihydrate

Cat.No: T6340

Synonym: 依那普利拉二水合物,MK-422,MK-422 Dihydrate

Target: RAAS, Autophagy

Temocapril hydrochloride

Cat.No: T6698

Synonym: CS-622 HCl,Acecol,Temocapril HCl,CS-622,盐酸替莫普利

Target: RAAS

Nitrosoglutathione

Cat.No: T19930

Synonym: S-Nitrosoglutathione,S-亚硝基谷胱甘肽,SNOG,Glutathione thionitrite,GSNO

Target: RAAS, NO Synthase

Angiotensin 1/2 (1-9) TFA(34273-12-6(free base))

Cat.No: T7663L

Target: Others

Delapril hydrochloride

Cat.No: T3281

Synonym: indalapril,地拉普利盐酸盐,Alindapril Hydrochloride,Delapril Hydrochloride,盐酸地拉普利,CV 3317

Target: RAAS

Perindopril erbumine

Cat.No: T1484L

Synonym: 培哚普利叔丁胺,培哚普利叔丁胺盐,S9490-3,Perindopril tert-butylamine salt

Target: Apoptosis, RAAS, MRP

Losartan potassium

Cat.No: T0215

Synonym: DuP-753 potassium,洛沙坦钾,氯沙坦钾,MK 954,DuP 753

Target: RAAS

H-Val-Pro-Pro-OH

Cat.No: T7354

Target: RAAS

Cat.No: T5964

Synonym: CS 088,奥美沙坦,RNH 6270

Target: RAAS

Abz-FR-K(Dnp)-P-OH acetate(500799-61-1 free base)

Cat.No: TP1682L

Target: Others

Cat.No: T1462

Synonym: SQ 14225,甲巯丙脯酸,卡托普利,SQ-14534,SA333

Target: RAAS

Cat.No: T25515

Synonym: I5 B2,I5-B2

Cat.No: T3281L

Synonym: Alindapril

Cat.No: T25094

Synonym: I5B1,I5 B1,K-4,K4,I5-B1

Cat.No: T1615L

Synonym: Irbesartan hydrochloride,BMS186295,BMS 186295,BMS-186295

Cat.No: T29702

Synonym: AG-85-12,AG85-12

Angiotensin 1/2 (1-9)

Cat.No: T7663

Target: Others

Angiotensin-converting enzyme

Cat.No: T76169

Angiotensin Fragment 1-7 (acetate)

Cat.No: T22575

Target: Others

Angiotensin 1/2 (1-7) amide

Cat.No: T22572

Target: Others

Cat.No: T28632

Synonym: RXP407

Angiotensin 1/2 (2-7)

Cat.No: T22573

Target: Others

Chlorambucyl-proline

Cat.No: T25238

Deserpidine hydrochloride

Cat.No: T71787

Angiotensinogen (1-14), human

Cat.No: TP1842

Cat.No: T19631

Synonym: PD-109488,Quinapril Diketopiperazine,PD109488

Abz-FR-K(Dnp)-P-OH

Cat.No: TP1682

Trandolaprilate hydrate

Cat.No: T72318

Synonym: Trandolaprilat hydrate ; RU 44403 hydrate,RU 44403 hydrate,Trandolaprilat hydrate

Cat.No: T62005

Cat.No: T76246

Cat.No: T68435

Hippuryl-His-Leu-OH

Cat.No: T76610

Cat.No: T71065

Cat.No: T75733

H-Val-Pro-Pro-OH TFA

Cat.No: T62297

Fosinopril-d7 sodium salt

Cat.No: T71205

Angiotensin II human TFA

Cat.No: T74142

Cat.No: T68616

Spirapril hydrochloride

Cat.No: T63425

Cat.No: T83768

Synonym: Zofenopril-SH,SQ 26,333

Cat. No.	Product Name	Target	Signaling Pathways
T5796	Plantainoside D Isoplantamajoside,车前草苷D	RAAS; PKC	Chromatin/Epigenetic; Cytoskeletal Signaling; Endocrinology/Hormones
	Plantainoside D (Isoplantamajoside) 可以抑制 ACE ，IC50=2.17 mM。Plantainoside D 也是IKK-β抑制剂。
TCS1704	Artemitin 艾黄素,Artemetin,Artemisetin,Erianthin	Antioxidant	oxidation-reduction
	Artemitin (Erianthin) 是一种存在于翼齿六棱菊中的天然黄酮，具有抗氧化、抗炎、抗病毒活性。
T5S0106	Peimisine 贝母辛,Ebeiensine	RAAS; AChR	Endocrinology/Hormones; Neuroscience
	Peimisine (Ebeiensine) 非竞争性拮抗气管平滑肌 M 受体，抑制 Ach 引起的平滑肌收缩。它兴奋 β 受体和拮抗内钙释放，促进一氧化氮释放，可舒张气管平滑肌，有平喘作用。
TN2487	1,3,5,6-Tetrahydroxyxanthone	Others	Others
	1,3,5,6-Tetrahydroxyxanthone shows moderate hepatoprotective activity with EC(50) values of 160.2 +/- 0.6 microM against tacrine-induced cytotoxicity in HepG2 cells. It can inhibit angiotensin-I-converting-enzyme activity in a dose-dependent manner.

天然产物

Plantainoside D

Cat.No: T5796

Synonym: Isoplantamajoside,车前草苷D

Target: RAAS, PKC

Cat.No: TCS1704

Synonym: 艾黄素,Artemetin,Artemisetin,Erianthin

Target: Antioxidant

Cat.No: T5S0106

Synonym: 贝母辛,Ebeiensine

Target: RAAS, AChR

1,3,5,6-Tetrahydroxyxanthone

Cat.No: TN2487

Target: Others

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