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。 | |||
T36622 |
Angiotensin I/II (1-6) (TFA)
|
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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... | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
T3281L |
Delapril
Alindapril |
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Delapril is an ACE inhibitor. It blocks the conversion of angiotensin I to angiotensin II. | |||
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. | |||
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 | |||
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 | |||
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
|
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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。 | |||
T71787 |
Deserpidine hydrochloride
|
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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... | |||
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 | |||
T19631 |
PD 109488
PD-109488,Quinapril Diketopiperazine,PD109488 |
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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. | |||
T75733 |
Saralasin TFA
|
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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。 | |||
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。 | |||
T74142 |
Angiotensin II human TFA
|
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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。 | |||
T63425 |
Spirapril hydrochloride
|
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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。 |