67
3
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T13920L |
Terlipressin Acetate
Terlipressin diacetate anhydrous,Terlipressin acetate anhydrous,醋酸特利加压素 |
Vasopressin Receptor | GPCR/G Protein |
Terlipressin Acetate 是一种高度选择性的加压素 V1 受体激动剂,对氧和葡萄糖剥夺/再氧合 (OGD/R) 诱导的肠上皮细胞损伤 (IEC-6) 具有抗炎和抗氧化作用,可用于肝肾综合征和耐去甲肾上腺素的败血性休克的研究。 | |||
T2568L |
Felypressin acetate
2-(L-Phenylalanine)-8-L-lysinevasopressin,醋酸苯赖加压素,PLV2. H-Cys-Phe-Phe-Gln-Asn-Cys-Pro-Lys-Gly-NH2 (Disulfide bond),PLV 2,PLV-2 |
Vasopressin Receptor | GPCR/G Protein |
Felypressin acetate (PLV-2) 是加压素 1 的激动剂,作用于所有精氨酸加压素受体 1AS。 Felypressin acetate 可用于牙科手术。 | |||
T2568 |
Felypressin
Octapressin,Felypressin Acetate,PLV-2,H-[Cys-Phe-Phe-Gln-Asn-Cys]-Pro-Lys-Gly-NH2,苯赖加压素 |
Vasopressin Receptor | GPCR/G Protein |
Felypressin (Octapressin) 是一种加压素 1 激动剂,也是血管收缩剂,可用于牙科手术中。 | |||
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。 | |||
TP2165 |
Urotensin II, mouse acetate (9047-55-6 free base)
Urotensin II, mouse acetate |
GPR | Endocrinology/Hormones; GPCR/G Protein |
Urotensin II, mouse acetate (9047-55-6 free base) 是孤儿 GPR14 或 SENR 的内源性配体。它是一种强效血管收缩剂。 | |||
TP1737L |
Urotensin II (114-124), human acetate
Urotensin II (114-124), human acetate(251293-28-4 free base) |
GPR | Endocrinology/Hormones; GPCR/G Protein |
Urotensin II (114-124), human acetate(251293-28-4 free base) 是一种 11 个氨基酸残基肽,是一种有效的血管收缩剂和孤儿受体 GPR14 的激动剂。 | |||
T0045 |
Heptaminol hydrochloride
盐酸庚胺醇,RP-2831 hydrochloride |
Others | Others |
Heptaminol hydrochloride (RP-2831 hydrochloride) 是一种血管收缩剂,有用于低血压(特别是体位性低血压)的研究潜力。 | |||
T12924 |
Sitaxsentan
TBC-11251,IPI 1040 |
Endothelin Receptor | GPCR/G Protein |
Sitaxsentan (TBC-11251) 是选择性内皮素A (ETA) 受体拮抗剂。内皮素是一种有效的血管收缩剂。Sitaxsentan 阻断内皮素与其受体的结合,从而消除内皮素的有害作用。 | |||
T19309L1 |
Endothelin 1 (swine, human) acetate
Endothelin 1 (swine, human) acetate(117399-94-7 free base) |
Endothelin Receptor | GPCR/G Protein |
Endothelin 1 (swine, human) acetate(117399-94-7 free base) 是一种合成肽,其序列为人和猪内皮素 1。它是一种有效的内源性血管收缩剂,通过两种类型的受体 ETA 和 ETB 起作用。 | |||
TP1049L |
Ornipressin Acetate(3397-23-7,free)
鸟氨酸加压素,Orpressin,POR-8 |
Others | Others |
Ornipressin Acetate (POR-8) 是一种有效的血管收缩剂、止血剂和肾脏剂。 | |||
T0446 |
Naphazoline hydrochloride
盐酸萘甲唑啉,Albalon,Rhinantin,Naphazoline HCl |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Naphazoline hydrochloride (Naphazoline HCl) 是一种咪唑啉衍生物,是一种眼血管收缩剂。 | |||
T7386 |
Bretylium tosylate
溴苄乙胺,托西溴苄铵 |
Others | Others |
Bretylium tosylate 是交感神经和肾上腺素神经的阻断剂,是血管收缩的神经递质突触前释放的抑制剂。 | |||
T21445 |
Naphazoline
AK-Con,Naphcon-a,Clear Eyes,All Clear,萘甲唑林 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Naphazoline (Naphcon-a) 是一种具有显着 α 肾上腺素能活性的拟交感神经化合物。 萘甲唑啉可用作血管收缩剂,当应用于粘膜时可快速减少肿胀。 | |||
T0948 |
Adrenalone hydrochloride
Adrenalone HCl,肾上腺酮盐酸盐,盐酸肾上腺酮 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Adrenalone hydrochloride (Adrenalone HCl) 是一种多巴胺β氧化酶 (dopamine β oxidase) 抑制剂,结构与去甲肾上腺素转运蛋白 (NET) 配体相似,IC50=36.9 μM。它是一种肾上腺素能 (adrenergic) 激动剂,用作局部血管收缩剂和止血剂。 | |||
T0279 |
Metaraminol tartrate
重酒石酸间羟胺,Metaradrine tartrate,Metaraminol bitartrate |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Metaraminol tartrate (Metaradrine tartrate) 是一种 α-肾上腺素能 (α-adrenergic) 激动剂,是一种直接或间接影响肾上腺素受体的拟交感神经胺,其中 α 效应占主导地位,可作为血管加压剂。 | |||
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。 | |||
T14021 |
20-HETE
20-hydroxy Arachidonic Acid |
Others | Others |
20-HETE (20-hydroxy Arachidonic Acid) is a CYP450 metabolite and a potent vasoconstrictor and it is an endogenous inhibitor of the large-conductance Ca2+-activated K+ channel in renal arterioles. 20-HETE increases NADPH oxidase, ROS, and NF-κB activity, a | |||
T8560 |
Angiotensin II human acetate
Ang II acetate,DRVYIHPF acetate,Angiotensin II acetate,血管紧张素II |
Apoptosis; RAAS | Apoptosis; Endocrinology/Hormones |
Angiotensin II human acetate (DRVYIHPF acetate) 是血管收缩剂,是肾素/血管紧张素系统的主要生物活性肽,在调节人类血压中起着核心作用。它刺激交感神经刺激,增加醛固酮生物合成和肾脏活动。它诱导血管平滑肌细胞生长,也诱导细胞凋亡。它通过 LOX-1 依赖的氧化还原敏感途径诱导内皮细胞毛细血管形成。 | |||
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。 | |||
TP1345 |
Kisspeptin-10, human (TFA)(374675-21-5,FREE)
|
GPR; Kisspeptin | Endocrinology/Hormones; GPCR/G Protein |
Kisspeptin-10, human (TFA)(374675-21-5,FREE) 是一种有效的血管收缩剂和血管生成抑制剂。 Kisspeptin-10,人类 TFA 通过其受体 GPR54 充当肿瘤转移抑制因子。 Kisspeptin-10-GPR54系统在胚胎肾发育中发挥重要作用。 Kisspeptin-10/GPR54 信号通过 NFATc4 介导的 BMP2 表达诱导成骨细胞分化 | |||
T6264 |
Bosentan
Actelion,波生坦,Ro 47-0203,Benzenesulfonamide |
Endothelin Receptor | GPCR/G Protein |
Bosentan (Benzenesulfonamide) 是 endothelin-1 (ET)拮抗剂,在人的 SMC 细胞中,它能够作用于 ETA 受体(Ki:4.7 nM)和 ETB 受体(Ki:95 nM)。 | |||
T6529 |
Halobetasol propionate
卤贝他索丙酸酯,Halobetasol Propionate,Ulobetasol propionate,BMY-30056,卤倍他索丙酸酯,CGP-14458 |
Phospholipase | Metabolism |
Halobetasol propionate (BMY-30056) 是一种在皮肤外使用的合成类固醇,具有抗炎,止痒和收缩血管的活性。 | |||
T0871 |
Noradrenaline bitartrate
|
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Noradrenaline bitartrate 直接作用于 α 和 β 肾上腺素能受体。它是去甲肾上腺素的酒石酸氢盐,去甲肾上腺素是一种合成苯乙胺,可模拟内源性去甲肾上腺素的拟交感神经作用。临床上,去甲肾上腺素用作外周血管收缩剂,通过其α-肾上腺素能作用导致动脉和静脉床收缩。它还被用作通过其 β-1 肾上腺素能作用介导的强效正性肌力和变时性心脏刺激剂。 | |||
T70216 |
Clonazoline
|
||
Clonazoline is a coronary vasodilator that is an imidazoline sympathomimetic, an alpha-adrenoreceptor agonist. It was used as a nasal decongestant and vasoconstrictor. | |||
T24603 |
PD-34799-SA
PD 34799-SA,PD34799-SA |
||
PD-34799-SA is an effective inhibitor of vasoconstrictor responses to sympathetic nerve stimulation. | |||
T24541 |
Norbormide
Mcneil 1025,S 6999,MCN 1025,Shoxin,Raticate |
||
Norbormide is a toxic compound used as a rodenticide. It has several mechanisms of action, acting as a vasoconstrictor and calcium channel blocker. | |||
TP1175 |
Endothelin-3, human, mouse, rabbit, rat
Endothelin 3 (Rat,Human) |
||
Endothelin-3, human, mouse, rabbit, rat , is a cyclic 21 amino acid peptide. It is an endogenous neuropeptide and potent vasoconstrictor. | |||
T81652 |
Nordefrin
(±)-Cobefri |
||
Nordefrin ((±)-Cobefri)为Norepinephrine的衍生物,具有血管收缩作用。 | |||
TP1522 |
Angiotensin II (5-8), human
|
||
Angiotensin II (5-8) is an endogenous C-terminal fragment of the peptide vasoconstrictor angiotensin II | |||
T69670 | Clonazoline HCl | ||
Clonazoline HCl is the salt form of Clonazoline, a coronary vasodilator that is an imidazoline sympathomimetic, an alpha-adrenoreceptor agonist. It was used as a nasal decongestant and vasoconstrictor. | |||
TP1737 |
Urotensin II (114-124), human
|
||
Urotensin II (114-124), human, is an 11-amino acid residue peptide that exhibits strong vasoconstrictor activity and acts as an agonist for the orphan receptor GPR14. | |||
T76564L |
Endothelin-1 (1-31) (Human) acetate
|
||
Endothelin-1 (1-31) (Human) acetate,源自于chymase对大ET-1的选择性水解,是一种有效的血管收缩剂和血压升高剂。 | |||
T13920 |
Terlipressin
|
Others | Others |
Terlipressin is a potent vasoconstrictor that acts via V1 receptors on arteriolar smooth muscle cells. | |||
T19309 |
Endothelin 1 (swine, human)
|
Others | Others |
Endothelin 1 (swine, human), a synthetic peptide mirroring the sequence of both human and swine Endothelin 1, functions as a robust endogenous vasoconstrictor by interacting with two receptor types, ETA and ETB. | |||
TP1661 |
Angiotensin II (1-4), human TFA
|
||
Angiotensin II is a potent direct vasoconstrictor, causing arteries and veins to constrict, so leading to an increase in blood pressure. | |||
T25199 |
Cafaminol
Cafaminolum,G1,G-1,G 1 |
||
Cafaminol (methylcoffanolamine) is a vasoconstrictor and anticatarrhal of the methylxanthine family related to caffeine which is used as a nasal decongestant. | |||
TP1049 |
Ornipressin
POR-8,鸟氨酸加压素 |
||
Ornipressin is a vasoconstrictor, haemostatic and renal agent. | |||
TP1396 |
Kisspeptin-10, human
|
||
Kisspeptin-10, human is an effective vasoconstrictor and inhibitor of angiogenesis. | |||
T0279L2 |
Metaraminol hydrochloride
Metaraminol HCl |
||
Metaraminol hydrochloride, used primarily as a vasoconstrictor in the treatment of HYPOTENSION, is a sympathomimetic agent that acts predominantly at alpha-1 adrenergic receptors. | |||
T78063 |
Endothelin-1 (1-31) (Human) TFA
|
ERK | MAPK |
Endothelin-1 (1-31) (Human) TFA 是源自chymase对大ET-1选择性水解的一种有效血管收缩剂和血压升高剂。 | |||
T37227 |
(±)8(9)-DiHET
|
||
Epoxide hydrolases convert the EETs into vicinal diols, with the concurrent loss of much of their biological activity. The 8(S),9(R)-EET isomer is metabolized by platelet COX to form 8(S),9(R),11(R)-THETA, a trihydroxy fatty acid which may act as a renal vasoconstrictor. | |||
T76564 |
Endothelin-1 (1-31) (Human)
|
||
Endothelin-1 (1-31) (Human) 是源于chymase对大ET-1选择性水解而来的有效血管收缩剂和血压升高剂。 | |||
TP1415 |
Urotensin II (114-124), human TFA
|
||
Urotensin II (114-124), human TFA, is an 11-amino acid residue peptide with a strong vasoconstrictor effect. This compound acts as an agonist for the orphan receptor GPR14. | |||
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. | |||
TP2166 |
Urotensin II, mouse TFA (9047-55-6 free base)
Urotensin II, mouse TFA |
GPR | Endocrinology/Hormones; GPCR/G Protein |
Urotensin II, mouse TFA is an endogenous ligand for the orphan GPR14 or SENR. It is a potent vasoconstrictor. | |||
T75962 |
Urotensin II, mouse acetate
|
||
Urotensin II, mouse acetate,是孤儿G蛋白偶联受体(GPR14或SENR)的一种内源性配体,具有显著的血管收缩活性并在中枢神经系统中发挥重要功能。 | |||
T68825 |
Doxazosin HCl
|
||
Doxazosin HCl is the salt form of Doxazosin Free Base which acts by inhibiting the postsynaptic alpha(1)-adrenoceptors on vascular smooth muscle. This inhibits the vasoconstrictor effect of circulating and locally released catecholamines (epinephrine and norepinephrine), resulting in peripheral vasodilation. | |||
T36479 |
Big Endothelin-1 (1-38), human
|
||
Human Big ET-1 comprises residues 53-90 of the endothelin precursor (preproendothelin). Compared to the mature endothelin-1 (hET-1), the peptide show less vasoconstrictor activity in vitro, but similar pressor effects in vivo. Former CAS-number 121014-53-7. | |||
T76081 |
Endothelin 1 (swine, human), Alexa Fluor 488-labeled
|
||
Endothelin 1 (swine, human), Alexa Fluor 488-labeled 是标记了488 荧光的 Endothelin 1 合成肽。Endothelin 1 (swine, human) 是具有人和猪内皮素 1 序列的合成肽,是有效的内源性血管收缩剂。Endothelin 1 通过两种类型受体 ETA 和 ETB 发挥作用。 | |||
T75961 |
Urotensin II, mouse TFA
|
||
Urotensin II, mouse TFA 为孤儿G蛋白偶联受体GPR14或SENR的内源性配体,具有强效血管收缩作用,并在中枢神经系统中发挥重要角色。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T1287 |
Synephrine
辛弗林,Oxedrine |
Endogenous Metabolite; Adrenergic Receptor | GPCR/G Protein; Metabolism; Neuroscience |
Synephrine (Oxedrine) 是来自 Citrus aurantium 的α-adrenergic 和β-adrenergic 激动剂,是一种生物碱。它也是一种拟交感神经化合物,能够用于减肥。 | |||
T7040 |
Angiotensin II human
DRVYIHPF,Angiotensin II,Hypertensin II,血管紧张素Ⅱ,Ang II,血管紧张素II |
Apoptosis; RAAS | Apoptosis; Endocrinology/Hormones |
Angiotensin II human (Ang II) 是一种生物活性肽,一种血管收缩剂。Angiotensin II 可以与 AT1R 和 AT2R 相互作用,调节人类血压,刺激交感神经,增加醛固酮生物合成和肾脏活动。 | |||
TN6575 | Pilosidine | ||
Pilosidine has vasoconstrictor activity, it showed facilitating effect on adrenaline evoked contractions in rabbit aorta isolated preparations. |