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Search Results for " aldosterone "

44

抑制剂 & 化合物

9

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T19185	Aldosterone-d8 醛固酮 D8,Aldosterone D8	Others	Others
	Aldosterone D8, a deuterium-labeled variant of Aldosterone produced in the adrenal zona glomerulosa, regulates blood pressure.
T36381	Aldosterone 21-sulfate (sodium salt)
	Aldosterone 21-sulfate is a metabolite of the steroid hormone aldosterone .1It reduces the sodium-to-potassium ratio in rat urine when administered at doses ranging from 10 to 100 μg, indicating mineralocorticoid activity that is less than 1% that of aldosterone.2 1.Grose, J.H., Nowaczynski, W., Kuchel, O., et al.Isolation of aldosterone urinary metabolites, glucuronides and sulfateJ. Steroid Biochem.4(6)551-566(1973) 2.Jowett, T.P., and Slater, J.D.H.Aldosterone 21-sulphate in manJ. Steroid. Bi...
T29852	Aldosterone-3-(O-carboxymethyl)oximino-(2-iodohistamine)
	Aldosterone-3-(O-carboxymethyl)oximino-(2-iodohistamine) is a biochemical.
T4316	ML365	Potassium Channel	Membrane transporter/Ion channel
	ML365 是有效的，选择性的双孔结构域钾通道TASK1/KCNK3抑制剂，IC50为 4 nM。它可用于检查 TASK1 通道的特定作用。
T1410	Torsemide AC-4464,JDL-464,托拉塞米,Torasemide	Na-K-Cl cotransporter	Membrane transporter/Ion channel
	Torsemide (AC-4464) 是具有口服活性的亨氏环利尿剂，也具有抗醛固酮和血管舒张活性。它可用于研究心力衰竭、肾脏疾病、肝硬化。
T0083	Eplerenone Epoxymexrenone,CGP 30083,依普利酮,SC-66110	Glucocorticoid Receptor	Endocrinology/Hormones
	Eplerenone (CGP 30083) 是一种竞争性的、选择性的、具有口服活性的醛固酮 (aldosterone) 拮抗剂，IC50=138 nM。它对孕酮，雄激素，雌激素和糖皮质激素受体的亲和力低，可用于研究高血压和心肌梗死后的心力衰竭。
T0293	Metyrapone 美替拉酮,甲吡酮,NSC-25265,Su-4885	Others; P450; Dehydrogenase; Autophagy	Autophagy; Metabolism; Others
	Metyrapone (NSC-25265) 是 STEROID 11-BETA-MONOOXYGENASE 酶抑制剂。它被用作库欣综合征诊断中下丘脑-垂体反馈机制的测试。
T4277	Osilodrostat LCI699	Glucocorticoid Receptor; Others; Hydroxylase	Endocrinology/Hormones; Metabolism; Others
	Osilodrostat (LCI699) 是一种有效的人11β-羟化酶和醛固酮合成酶抑制剂，IC50分别值为2.5 和0.7nM。
T13881	Dicirenone SC26304	ATPase; Glucocorticoid Receptor	Endocrinology/Hormones; Membrane transporter/Ion channel
	Dicirenone (SC26304) 对盐皮质激素受体（MR）有抑制作用，对醛固酮对尿 K+:Na+ 比例的调节和醛固酮与肾细胞质和核受体结合有抑制作用。
T0476	Spironolactone 安体舒通,螺内酯,SC9420,Abbolactone	Glucocorticoid Receptor; Androgen Receptor; Autophagy	Autophagy; Endocrinology/Hormones
	Spironolactone (SC9420) 是一种可口服的醛固酮盐皮质激素受体拮抗剂，IC50值为 24 nM。它也是雄激素受体拮抗剂，促进足细胞自噬，IC50值为 77 nM。
T71664	Mespirenone	Others	Others
	Mespirenone 是一种具有利尿作用的螺内酯衍生物和醛固酮拮抗剂。
T61373	Baxdrostat	Others	Others
	Baxdrostat 是一种醛固酮合成酶抑制剂。
T6262	Evacetrapib LY2484595	CETP	Metabolism
	Evacetrapib (LY2484595) 是 CETP 的选择性抑制剂，在人血浆中，抑制人重组 CETP 蛋白 (IC50:5.5 nM) 和 CETP (IC50:36 nM) 活性。
T3096	Canrenoate potassium 坎利酸钾,Potassium aldadiene,Canrenoic acid potassium salt,Potassium canrenoate,Soldactone	Glucocorticoid Receptor	Endocrinology/Hormones
	Canrenoate potassium (Soldactone) 是一种有效的竞争性盐皮质激素受体 (mineralocorticoid receptor) 拮抗剂，是一种释放 canrenone 的前药。它作为一种利尿剂，用于高血压的研究。
T1866	AT-56	Others; PGE Synthase	Immunology/Inflammation; Others
	AT56 是口服有活性的脂钙蛋白型前列腺素 D 合酶 (L-PGDS) 选择性抑制剂，其IC50=95 μM，Ki=75 μM。它能够特异性地抑制L-PGDS 催化的 PGD2介导的嗜睡或疼痛反应。
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。
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。
T69041	SC 11927
	SC 11927 is an aldosterone antagonist.
T26157	RU 752 RU-752,RU752
	RU 752 is an antagonist of mineralocorticoid receptor that inhibits aldosterone synthesis.
T70242	SC 8109
	SC 8109 is an aldosterone antagonist.
T34430	RU 24411 RU24411,RU-24411
	RU 24411是一种合成的19-nor 类固醇化合物。在没有葡萄糖的情况下，RU 24411 与醛固酮一样能够刺激钠的转运。
T69705	SC 19886
	SC 19886 is an antimineralocorticoid that acts as a potent inhibitor of aldosterone biosynthesis.
T76646	Acetyl-ACTH (7-24) (human, bovine, rat)
	Acetyl-ACTH (7-24) (human, bovine, rat) 可导致 ACTH 诱发的皮质酮和醛固酮释放显著减少。
T14664	BI 689648	Others	Others
	BI 689648 is a highly selective inhibitor of aldosterone synthase(CYP11B1 and CYP11B2 with IC50s of 310 and 2.1 nM, respectively).
T62747	Lorundrostat
	Lorundrostat 是一种醛固酮合酶 (aldosterone synthase) 抑制剂。
T69273	Mexrenoate potassium
	Mexrenoate potassium is a steroidal aldosterone antagonist and antihypertensive.
T68699	Oxprenoate Free Base
	Oxprenoate Free Base is a mineralocorticoid receptor (MR) antagonist, inhibiting aldosterone production and secretion.
T61372	(S)-Baxdrostat
	(S)-Baxdrostat is an S-enantiomer of Baxdrostat, which functions as an inhibitor of aldosterone synthase [1].
T69284	SC 23133
	SC 23133 is an antimineralocorticoid that is known to induce a marked but reversible inhibition of aldosterone biosynthesis.
T38424	(R)-Fadrozole FAD286,(R)-CGS 16949A free base,(R)-Fadrozole
	(R)-Fadrozole ((R)-CGS 16949A; FAD286) is a potent nonsteroidal inhibitor. (R)-Fadrozole also inhibits human placental aromatase (pIC 50 = 6.17) and aldosterone biosynthesis. (R)-Fadrozole reverses cardiac fibrosis in spontaneously hypertensive heart failure rats..
T68009	prorenoate
	Prorenoate 是一种甾体醛固酮拮抗剂，具有保钾利尿作用。Prorenoate 可拮抗醛固酮在肾元中盐皮质激素受体的活性，从而阻止钠的重吸收。这会干扰钠/钾交换器，导致钠和水排泄，同时减少钾排泄。
T83495	[D-Pro4,D-Trp7,9] Substance P (4-11)
	[D-Pro4,D-Trp7,9]Substance P(4-11)为高效Substance P 拮抗剂，可降低血浆醛固酮(ALDO)浓度。
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.
T80687	γ3-MSH
	γ3-MSH 源于 pro-opiomelanocortin (POMC) 的 N 端，能够激活人肾上腺肿瘤细胞分泌醛固酮。
TP1209	BNP (1-32), rat TFA (133448-20-1 free base) Brain Natriuretic Peptide (BNP) (1-32), rat TFA,BNP (1-32), rat TFA
	Acts as a cardiac hormone with a variety of biological actions including natriuresis, diuresis, vasorelaxation, and inhibition of renin and aldosterone secretion. It is thought to play a key role in cardiovascular homeostasis. Helps restore the body\'s sa
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...
T76334	Cenderitide
	Cenderitide 是一种有效的颗粒鸟酰基环化酶受体 (pGC) 激动剂。Cenderitide 是一种由 C 型利钠肽 (CNP) 与石斛利钠肽 (DNP) 的 C 端融合而成的利钠肽 (NP) 。Cenderitide 可激活 pGC-A 和 pGC-B，激活第二信使 cGMP，抑制醛固酮 (aldosterone)，在不降低血压的情况下保持 GFR 。Cenderitide 可用于心力衰竭的研究。
T68808	11-Dehydrocorticosterone
	11-Dehydrocorticosterone is an endogenous mineralocorticoid. It increases Na+/K+-ATPase mRNA expression in vascular smooth muscle cells and inhibits aldosterone action in B. marinus toad bladder tissue in a concentration-dependent manner. 11-Dehydrocorticosterone decreases the sodium/creatine ratio and increases the potassium/creatine ratio in rat urine in a dose-dependent manner in a model of 11β-hydroxysteroid dehydrogenase inhibition induced by carbenoxolone. Chronic administration 11-dehydro...
T83501	[Deamino-Pen1,Val4,D-Arg8]-vasopressin	Vasopressin Receptor	GPCR/G Protein
	"[Deamino-Pen1,Val4,D-Arg8]-vasopressin (AVP-A)是一种作用于精氨酸血管加压素(AVP)的拮抗剂，它能有效地降低大鼠血浆中的醛固酮浓度。本化合物主要应用于研究大鼠肾上腺球状带的生长及其类固醇生成作用。"
T31845	Forasartan SC52458,SC 52458,SC-52458
	Forasartan is a non - peptide angiotensin II receptor antagonist with antihypertensive activity. Forasartan and angiotensin II compete to bind AT1 receptor subtypes in vascular smooth muscle, thereby blocking angiotensin II-mediated vasoconstriction, lead
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
T73896	Glucose-6-phosphate dehydrogenase
	Glucose-6-phosphate dehydrogenase 是戊糖磷酸途径的限速酶。Glucose-6-phosphate dehydrogenase 是抗氧化途径、一氧化氮合酶、NADPH 氧化酶、细胞色素 p450 等系统中 NADPH 的主要来源。Glucose-6-phosphate dehydrogenase 可用于糖尿病、醛固酮诱导的内皮功能障碍和癌症的研究。
T68765	Spirorenone
	Spirorenone is an androstadienone derivative as a highly effective aldosterone antagonist. Spirorenone is 8.6 times as potent as spironolactone, but showed a lower affinity for the mineralocorticoid receptors. In phase I clinical trials Spirorenone was absorbed with a half-life of 20-30 min, achieving maximum concentrations of about 100 ng/ml (10 mg) and 260 ng/ml (40 mg) after 1-2 h. Disposition of the parent drug was biphasic with half-lives of 50-60 min (distribution) and 5-6 h (elimination)....
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。

化合物

Aldosterone-d8

Cat.No: T19185

Synonym: 醛固酮 D8,Aldosterone D8

Target: Others

Aldosterone 21-sulfate (sodium salt)

Cat.No: T36381

Aldosterone-3-(O-carboxymethyl)oximino-(2-iodohistamine)

Cat.No: T29852

Cat.No: T4316

Target: Potassium Channel

Cat.No: T1410

Synonym: AC-4464,JDL-464,托拉塞米,Torasemide

Target: Na-K-Cl cotransporter

Cat.No: T0083

Synonym: Epoxymexrenone,CGP 30083,依普利酮,SC-66110

Target: Glucocorticoid Receptor

Cat.No: T0293

Synonym: 美替拉酮,甲吡酮,NSC-25265,Su-4885

Target: Others, P450, Dehydrogenase, Autophagy

Cat.No: T4277

Synonym: LCI699

Target: Glucocorticoid Receptor, Others, Hydroxylase

Cat.No: T13881

Synonym: SC26304

Target: ATPase, Glucocorticoid Receptor

Cat.No: T0476

Synonym: 安体舒通,螺内酯,SC9420,Abbolactone

Target: Glucocorticoid Receptor, Androgen Receptor, Autophagy

Cat.No: T71664

Target: Others

Cat.No: T61373

Target: Others

Cat.No: T6262

Synonym: LY2484595

Target: CETP

Canrenoate potassium

Cat.No: T3096

Synonym: 坎利酸钾,Potassium aldadiene,Canrenoic acid potassium salt,Potassium canrenoate,Soldactone

Target: Glucocorticoid Receptor

Cat.No: T1866

Target: Others, PGE Synthase

Angiotensin I (human, mouse, rat)

Cat.No: TP1295

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

Target: Others

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

Cat.No: T69041

Cat.No: T26157

Synonym: RU-752,RU752

Cat.No: T70242

Cat.No: T34430

Synonym: RU24411,RU-24411

Cat.No: T69705

Acetyl-ACTH (7-24) (human, bovine, rat)

Cat.No: T76646

Cat.No: T14664

Target: Others

Cat.No: T62747

Mexrenoate potassium

Cat.No: T69273

Oxprenoate Free Base

Cat.No: T68699

Cat.No: T61372

Cat.No: T69284

Cat.No: T38424

Synonym: FAD286,(R)-CGS 16949A free base,(R)-Fadrozole

Cat.No: T68009

[D-Pro4,D-Trp7,9] Substance P (4-11)

Cat.No: T83495

Cat.No: T19631

Synonym: PD-109488,Quinapril Diketopiperazine,PD109488

Cat.No: T80687

BNP (1-32), rat TFA (133448-20-1 free base)

Cat.No: TP1209

Synonym: Brain Natriuretic Peptide (BNP) (1-32), rat TFA,BNP (1-32), rat TFA

Deserpidine hydrochloride

Cat.No: T71787

Cat.No: T76334

11-Dehydrocorticosterone

Cat.No: T68808

[Deamino-Pen1,Val4,D-Arg8]-vasopressin

Cat.No: T83501

Target: Vasopressin Receptor

Cat.No: T31845

Synonym: SC52458,SC 52458,SC-52458

Angiotensin 1/2 (2-7)

Cat.No: T22573

Target: Others

Glucose-6-phosphate dehydrogenase

Cat.No: T73896

Cat.No: T68765

Angiotensin II human TFA

Cat.No: T74142

Cat. No.	Product Name	Target	Signaling Pathways
T19186	Aldosterone	Others	Others
	Aldosterone is the primary mineralocorticoid. Aldosterone is synthesized and secreted in response to renin-angiotensin system activation or high dietary potassium by the zona glomerulosa of the adrenal cortex.
T3033	Deoxycorticosterone acetate 醋酸去氧皮质酮,DOC acetate,Cortexone acetate,11-Deoxycorticosterone acetate,醋酸脱氧皮质酮	Glucocorticoid Receptor; Endogenous Metabolite; Adrenergic Receptor	Endocrinology/Hormones; GPCR/G Protein; Metabolism; Neuroscience
	Deoxycorticosterone acetate (Cortexone acetate) 是肾上腺产生的类固醇激素，具有盐皮质激素活性，并作为醛固酮的前体。
T0354	Canrenone 6,7-Dehydro-7α-desthioacetylspironolactone,SC9376,Aldadiene,坎利酮,RP-11614,SC14266	Glucocorticoid Receptor; Endogenous Metabolite	Endocrinology/Hormones; Metabolism
	Canrenone (SC14266) 是一种醛固酮 (aldosterone) 拮抗剂，广泛用作利尿剂。
T20302	Deoxycorticosterone Desoxycorticosterone,去氧皮质酮,Desoxycorticosteronum,Desoxycortone	Endogenous Metabolite	Metabolism
	Deoxycorticosterone (Desoxycortone) 是由肾上腺产生的类固醇代谢物。 Deoxycorticosterone 是醛固酮前体，具有盐皮质激素活性。
T67319	2',4'-Dimethylacetophenone	Endogenous Metabolite	Metabolism
	2',4'-Dimethylacetophenone 是一种可用于生物研究的化学物。该化合物可用于气相色谱法检测烟草化合物中的醛固酮香气，可以用于保护食品。
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。
T0522	Diammonium Glycyrrhizinate 甘草酸二铵,Glycyrrhizin	Dehydrogenase	Metabolism
	Diammonium Glycyrrhizinate (Glycyrrhizin) 是分离自甘草中的化合物，有抗炎作用。
T8270	Deserpidine 地舍平,Harmonyl	RAAS	Endocrinology/Hormones
	Deserpidine (Harmonyl) 是从 Rauwolfia canescens 的根中分离的生物碱。Deserpidine 与 Reserpine 相关。Deserpidine 是竞争性血管紧张素转化酶抑制剂，可以被用作抗高血压药以及镇定剂。Deserpidine 还减少了肾上腺皮质血管紧张素 II 诱导的醛固酮分泌。
T39991	18-Oxocortisol
	18-Oxocortisol is a cortisol derivative generated by aldosterone synthase (CYP11B2). It acts as a naturally occurring mineralocorticoid agonist and serves as a biomarker in adrenal vein sampling.

天然产物

Cat.No: T19186

Target: Others

Deoxycorticosterone acetate

Cat.No: T3033

Synonym: 醋酸去氧皮质酮,DOC acetate,Cortexone acetate,11-Deoxycorticosterone acetate,醋酸脱氧皮质酮

Target: Glucocorticoid Receptor, Endogenous Metabolite, Adrenergic Receptor

Cat.No: T0354

Synonym: 6,7-Dehydro-7α-desthioacetylspironolactone,SC9376,Aldadiene,坎利酮,RP-11614,SC14266

Target: Glucocorticoid Receptor, Endogenous Metabolite

Deoxycorticosterone

Cat.No: T20302

Synonym: Desoxycorticosterone,去氧皮质酮,Desoxycorticosteronum,Desoxycortone

Target: Endogenous Metabolite

2',4'-Dimethylacetophenone

Cat.No: T67319

Target: Endogenous Metabolite

Angiotensin II human

Cat.No: T7040

Synonym: DRVYIHPF,Angiotensin II,Hypertensin II,血管紧张素Ⅱ,Ang II,血管紧张素II

Target: Apoptosis, RAAS

Diammonium Glycyrrhizinate

Cat.No: T0522

Synonym: 甘草酸二铵,Glycyrrhizin

Target: Dehydrogenase

Cat.No: T8270

Synonym: 地舍平,Harmonyl

Target: RAAS

Cat.No: T39991

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