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Search Results for " angiotensin 1/2 "

45

抑制剂 & 化合物

4

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T21708L	Angiotensin 1/2 + A (2 - 8) Acetate Angiotensin 1/2 + A (2 - 8) Acetate (51833-76-2 Free base)	Others	Others
	Angiotensin 1/2 + A (2 - 8) Acetate 是一种血管收缩剂。
T22574L	Angiotensin 1/2 (5-7) acetate	RAAS	Endocrinology/Hormones
	Angiotensin 1/2 (5-7) acetate 是一种具有 H2N-Ile-His-Pro-OH 序列的肽。血管紧张素是一种寡肽，是一种激素和一种强大的双肽原。它来源于前体分子血管紧张素原，一种在肝脏中产生的血清球蛋白。它在肾素-血管紧张素系统中起重要作用。
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。
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。
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
T22574	Angiotensin 1/2 (5-7)	Others	Others
	Angiotensin 1/2 (5-7) is a peptide with the sequence H2N-Ile-His-Pro-OH. Angiotensin is an oligopeptide and is a hormone and a powerful dipsogen. It is derived from the precursor molecule angiotensinogen, a serum globulin produced in the liver. It plays a
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
TP2220	Angiotensin 1/2 (1-8) amide	Others	Others
	Angiotensin 1/2 (1-8) amide (H2N-Asp-Arg-Val-Tyr-Ile-His-Pro-Phe-amide) is a peptide analog to angiotensin II that is used as a vasopressor agent in the treatment of certain types of shock and circulatory collapse. It is a potent vasoconstrictor and is us
TP1224	[Sar1, Ile8]-Angiotensin II TFA Angiotensin 2 TFA,AngiotensinII TFA
	[Sar1, Ile8]-Angiotensin II (TFA) is a peptide compound that exerts various effects on vascular smooth muscle. These effects include the contraction of normal arteries as well as the hypertrophy or hyperplasia of cultured cells or diseased vessels.
T1615	Irbesartan 厄贝沙坦,SR-47436,BMS-186295	Apoptosis; RAAS	Apoptosis; Endocrinology/Hormones
	Irbesartan (SR-47436) 是一种 1 型血管紧张素 II 受体拮抗剂，IC50为1.3 nM。
T1570	Telmisartan BIBR 277,替米沙坦	RAAS; Autophagy	Autophagy; Endocrinology/Hormones
	Telmisartan (BIBR 277) 是一种血管紧张素II 1型受体拮抗剂，能够抑制其活性，IC50值为 9.2 nM。
T1057	Azilsartan TAK-536,阿齐沙坦	RAAS	Endocrinology/Hormones
	Azilsartan (TAK-536) 是一种高活性的血管紧张素Ⅱ1型受体特异性拮抗剂(IC50:2.6 nM)。
T28482	Firibastat QGC 001,QGC-001,RB-150,RB150,QGC001,RB 150	Aminopeptidase	Metabolism
	Firibastat (RB150) 是一种具有口服活性的 EC33 前体药物。Firibastat 是一种首创的脑氨基肽酶 A(APA) 抑制剂 (Ki=200 nM)，选择性地抑制高血压大鼠脑血管紧张素 II 转化为血管紧张素 III，降低血压。
T37496L	Alamandine TFA	RAAS	Endocrinology/Hormones
	Alamandine TFA 是肾素-血管紧张素系统 (RAS) 的成员，是一种血管活性肽，是 G 蛋白偶联受体 MrgD 的内源性配体。它通过抗高血压作用来保护肾脏和心脏。
T76605	Abz-Ser-Pro-3-nitro-Tyr
	Abz-Ser-Pro-3-nitro-Tyr 是 ACE2 (angiotensin-converting enzyme-2) 的底物。
T35830	Dehydro Olmesartan
	Dehydro Olmesartan, deriving from Olmesartan, acts as an angiotensin II receptor (AT1R) antagonist and exhibits potential for the study of high blood pressure [1][2].
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...
T80048	Mca-YVADAP-Lys(Dnp)-OH TFA
	Mca-YVADAP-Lys(Dnp)-OH TFA为Caspase-1及血管紧张素转换酶2(ACE2)特异性的荧光底物。
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...
T70256	L-163491
	L-163491 is a drug which acts as a partial agonist of angiotensin II receptor type 1, and with lower affinity as an agonist of angiotensin II receptor type 2, mimicking the action of angiotensin II. Its practical applications to date have been limited to scientific research into the function of the angiotensin receptor system, but it has been suggested as a potential therapeutic agent for the treatment of inflammation of the lungs associated with certain viral diseases such as COVID-19.
T76090	Mca-YVADAP-Lys(Dnp)-OH
	Mca-YVADAP-Lys(Dnp)-OH 是caspase-1和血管紧张素转换酶 2 (ACE2) 的荧光底物。
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。
T76200	STIEEQAKTFLDKFNHEAEDLFYQSSLASWN
	STIEEQAKTFLDKFNHEAEDLFYQSSLASWN 是与血管紧张素转换酶 2 (ACE2) 相关的肽，适用于研究 ACE2 功能。
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。
T79266	Antihypertensive agent 2
	Antihypertensive agent 2 (Compound 4g) 为一种有效的血管紧张素 II 受体 1 拮抗剂，其降血压效能可与Losartan媲美或更胜一筹。
T35873	C19 Ceramide (d18:1/19:0) C19 Ceramide (d18:1/19:0)
	C19 Ceramide is a naturally occurring ceramide that has been found in J. juncea extracts as well as rat brain and mouse heart.[1],[2],[3] It is elevated in adult and decreased in juvenile whole rat brain extracts by 114 and 37%, respectively, following chronic ethanol exposure.[2] C19 Ceramide is also increased in mouse hearts following administration of angiotensin II.[3]
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。
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。
T35967	N-methyl-2-HOBA (hydrochloride)
	N-methyl-2-HOBA is a methylated form of the isoketal scavenger 2-HOBA .1It has low reactivity with isoketals and has no effect on hypertension induced by angiotensin II . N-methyl-2-HOBA has been used as a negative control for the activity of 2-HOBA in a mouse model of hypertension. 1.Kirabo, A., Fontana, V., de Faria, A.P.C., et al.DC isoketal-modified proteins activate T cells and promote hypertensionJ. Clin. Invest.124(10)4642-4656(2014)
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。
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。
T80587	Alunacedase alfa HrsACE2,GSK 2586881	SARS-CoV	Microbiology/Virology
	Alunacedase alfa (HrsACE2; GSK 2586881) 是一种人源重组的可溶性血管紧张素转化酶 2（hrsACE2）。作为转基因可溶性形态的 ACE2，Alunacedase alfa 能够减少 SARS-CoV-2 与细胞膜结合 ACE2 的竞争性进入，因此具有研究 SARS-CoV-2 的可能性。
T35847	16(R)-HETE
	Electrolyte and fluid transport in the kidney are regulated in part by arachidonic acid and its metabolites. 16-HETE is a minor CYP450 metabolite of arachidonic acid released by the kidney upon angiotensin II stimulation that demonstrates stereospecific biological activity. Electrolyte and fluid transport in the kidney are regulated in part by arachidonic acid and its metabolites. 16-HETE is a minor CYP450 metabolite of arachidonic acid released by the kidney upon angiotensin II stimulation that...
T36006	Olmesartan medoxomil impurity C
	Olmesartan medoxomil impurity C is an Olmesartan medoxomil impurity. Olmesartan medoxomil is a potent and selective angiotensin AT1 receptor inhibitor with IC50 of 66.2 μM. [1]. Senda A, et al. Effects of Angiotensin II Receptor Blockers on Metabolism of Arachidonic Acid via CYP2C8. Biol Pharm Bull. 2015;38(12):1975-9. [2]. Shah S, et al. Simultaneous Quantitative Analysis of Olmesartan Medoxomil and Amlodipine Besylate in Plasma by High-performance Liquid Chromatography Technique. J Young Phar...
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)。
T64011	GSK1820795A
	GSK1820795A 作为替米沙坦类似物是hGPR132a 的选择性拮抗剂。GSK1820795A 阻断了 N-acylamides 对表达hGPR132a 的酵母细胞的活化。GSK1820795A 也是血管紧张素 II 拮抗剂和部分PPARγ激动剂 (compound 38) 。
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。
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。
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。
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。
T36942	SSAA09E1 SSAA09E1
	SSAA09E1 is an inhibitor of severe acute respiratory syndrome coronavirus (SARS-CoV) viral entry.1It reduces infection of HEK293T cells transiently transfected with angiotensin-converting enzyme 2 (ACE2) by an HIV-based virus system pseudotyped with SARS-CoV surface glycoprotein (EC50= 6.7 μM). SSAA09E1 also inhibits the proteolytic activity of cathepsin L (IC50= 5.33 μM) but not cathepsin B when used at a concentration of 20 μM. 1.()
T83742	SBP1 TFA Spike Binding Peptide 1
	Spike binding peptide 1 (SBP1) 为对应于血管紧张素转换酶2 (ACE2) 的第21至43位氨基酸的肽。已将脂质纳米粒子 (LNPs) 包裹的抗病毒化合物奥司他韦磷酸盐与SBP1结合并通过体外研究评估其控制释放奥司他韦磷酸盐的长期潜力。SBP1 (2%) 固定于交联的羟基丙烯酸酯和乙基黄原酸乙酯网络，提高了对严重急性呼吸系统冠状病毒2(SARS-CoV-2)刺突糖蛋白，亦称表面糖蛋白，的网络捕获效率。
T75238	YS-49 monohydrate
	YS-49 (单水合物) 作为PI3K/Akt（RhoA的下游靶点）的激活剂，有效降低3-甲基胆碱处理的细胞中RhoA/PTEN的活性。此外，YS-49通过促进血红素加氧酶（HO-1）的表达，抑制血管紧张素II（Ang II）诱导的血管平滑肌细胞（VSMC）增殖。作为一种异喹啉化合物生物碱，YS-49因激活心脏β-adrenoceptors而显示出显著的正性肌力效应。
T60935	H-Tyr-Phe-OH
	H-Tyr-Phe-OH (L-Tyrosyl-L-phenylalanine) 可用作区分良性甲状腺结节和甲状腺癌的生物标志物。H-Tyr-Phe-OH 是一种口服活性的血管紧张素转换酶抑制剂，在50 μM 时抑制率为 48%。H-Tyr-Phe-OH 具有黄嘌呤氧化酶抑制活性 (降低尿酸) ，可调节中性粒细胞样细胞中 IL-8 的产生。
T35855	AAA
	AAA is an antagonist of G protein-coupled receptor 75 (GPR75).1It increases basal GPR75 protein levels and inhibits 20-HETE-induced reductions in GPR75 protein levels in PC3 cells. AAA (5 and 10 μM) also reduces 20-HETE-induced phosphorylation of EGFR, NF-κB, and Akt in, and cell migration of, PC3 cells.In vivo, AAA (10 mg/kg per day) reduces systolic blood pressure, albuminuria, renal angiotensin II levels, and cardiac hypertrophy in a Cyp1a1-Ren-2 transgenic rat model of malignant hypertension...

化合物

Angiotensin 1/2 + A (2 - 8) Acetate

Cat.No: T21708L

Synonym: Angiotensin 1/2 + A (2 - 8) Acetate (51833-76-2 Free base)

Target: Others

Angiotensin 1/2 (5-7) acetate

Cat.No: T22574L

Target: RAAS

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

Cat.No: T7663L

Target: Others

Angiotensin 1/2 (1-9)

Cat.No: T7663

Target: Others

Angiotensin 1/2 (2-7)

Cat.No: T22573

Target: Others

Angiotensin 1/2 (5-7)

Cat.No: T22574

Target: Others

Angiotensin 1/2 (1-7) amide

Cat.No: T22572

Target: Others

Angiotensin 1/2 (1-8) amide

Cat.No: TP2220

Target: Others

[Sar1, Ile8]-Angiotensin II TFA

Cat.No: TP1224

Synonym: Angiotensin 2 TFA,AngiotensinII TFA

Cat.No: T1615

Synonym: 厄贝沙坦,SR-47436,BMS-186295

Target: Apoptosis, RAAS

Cat.No: T1570

Synonym: BIBR 277,替米沙坦

Target: RAAS, Autophagy

Cat.No: T1057

Synonym: TAK-536,阿齐沙坦

Target: RAAS

Cat.No: T28482

Synonym: QGC 001,QGC-001,RB-150,RB150,QGC001,RB 150

Target: Aminopeptidase

Cat.No: T37496L

Target: RAAS

Abz-Ser-Pro-3-nitro-Tyr

Cat.No: T76605

Dehydro Olmesartan

Cat.No: T35830

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

Cat.No: T36622

Mca-YVADAP-Lys(Dnp)-OH TFA

Cat.No: T80048

Cat.No: T37496

Cat.No: T70256

Mca-YVADAP-Lys(Dnp)-OH

Cat.No: T76090

(+)-Chloroquine

Cat.No: T83602

STIEEQAKTFLDKFNHEAEDLFYQSSLASWN

Cat.No: T76200

Angiotensin II human TFA

Cat.No: T74142

Antihypertensive agent 2

Cat.No: T79266

C19 Ceramide (d18:1/19:0)

Cat.No: T35873

Synonym: C19 Ceramide (d18:1/19:0)

Ovalbumin (154-159)

Cat.No: T80099

Target: Angiotensin-converting Enzyme (ACE)

H-Ile-Pro-Pro-OH hydrochloride

Cat.No: T73810

N-methyl-2-HOBA (hydrochloride)

Cat.No: T35967

Angiotensin (1-7) (acetate)

Cat.No: T37495

Hippuryl-His-Leu-OH

Cat.No: T76610

Alunacedase alfa

Cat.No: T80587

Synonym: HrsACE2,GSK 2586881

Target: SARS-CoV

Cat.No: T35847

Olmesartan medoxomil impurity C

Cat.No: T36006

Captopril EP Impurity B

Cat.No: T74109

Cat.No: T64011

Captopril hydrochloride

Cat.No: T60383

Cat.No: T76613

Ovotransferrin (328-332)

Cat.No: T80100

Target: Angiotensin-converting Enzyme (ACE)

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

Cat.No: T75752

Cat.No: T36942

Synonym: SSAA09E1

Cat.No: T83742

Synonym: Spike Binding Peptide 1

YS-49 monohydrate

Cat.No: T75238

Cat.No: T60935

Cat.No: T35855

Cat. No.	Product Name	Target	Signaling Pathways
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。
T81229	Safflor yellow B
	Safflor yellow B 通过抑制血管紧张素 II 介导的人脐静脉细胞损伤，调节 Bcl-2/p22 (phox) 表达，展现出神经保护作用。
T75697	1-Methyl-2-[(4Z,7Z)-4,7-tridecadienyl]-4(1H)-quinolone
	1-Methyl-2-[(4Z,7Z)-4,7-tridecadienyl]-4(1H)-quinolone，为喹诺酮类生物碱，作用为二酰基甘油酰基转移酶抑制剂与血管紧张素II受体阻断剂，其IC50值依次为20.1 μM与34.1 μM。此化合物亦展现对幽门螺杆菌的有效抗活性，MIC值达10 μg/mL。

天然产物

Cat.No: TCS1704

Synonym: 艾黄素,Artemetin,Artemisetin,Erianthin

Target: Antioxidant

Cat.No: T5S0106

Synonym: 贝母辛,Ebeiensine

Target: RAAS, AChR

Safflor yellow B

Cat.No: T81229

1-Methyl-2-[(4Z,7Z)-4,7-tridecadienyl]-4(1H)-quinolone

Cat.No: T75697

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