49
7
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T10683 |
Carmoxirole hydrochloride
EMD 45609 hydrochloride,卡莫昔罗 |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Carmoxirole hydrochloride (EMD 45609 hydrochloride) 是一种外周多巴胺 D2 受体选择性激动剂,在体内具有降压活性。 | |||
T25828 |
Monatepil maleate
AJ2615,AJ 2615,AJ-2615 |
||
Monatepil maleate is an Antihypertensive agent. It is a calcium antagonist with alpha(1)-adrenergic receptor blocking activity | |||
T7686 |
Ramiprilat
|
RAAS | Endocrinology/Hormones |
Ramiprilat 是 Ramipril 的活性代谢物,是一种口服有活力的血管紧张素转换酶 (ACE) 抑制剂,其 Ki=7 pM。它可用于研究心力衰竭以及高血压。 | |||
T15553 |
Iganidipine
NKY 722 |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Iganidipine(NKY 722) 是一种新的水溶性 Ca2+ 拮抗剂,具有降压活性,可用于研究和神经系统相关的疾病。 | |||
T1605 |
Enalapril
MK-421,依那普利 |
RAAS; MRP | Endocrinology/Hormones; Immunology/Inflammation |
Enalapril 是一种血管紧张素转换酶(ACE)抑制剂。 | |||
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。 | |||
T22830 |
GYY4137
GYY 4137 morpholine salt |
Others | Others |
GYY4137 (GYY 4137 morpholine salt) 是一种缓释H2S 供体,具有抗炎和抗癌作用,也具有血管扩张和抗高血压活性。 | |||
T1520 |
Aliskiren hemifumarate
阿利克仑半富马酸盐,CGP 60536,SPP 100,CGP60536B |
RAAS; Autophagy | Autophagy; Endocrinology/Hormones |
Aliskiren hemifumarate (CGP60536B) 一种可口服非肽肾素抑制剂,IC50为1.5 nM,具有抗高血压活性。 | |||
T13154 |
Tiapamil hydrochloride
Ro 11-1781 hydrochloride,ORE 5002 hydrochloride |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Tiapamil hydrochloride (Ro 11-1781 hydrochloride) 是一种钙通道阻滞剂,具有抗高血压活性,可用于研究心绞痛和心血管疾病。 | |||
T60715 |
α-Glucosidase-IN-4
|
Glucosidase | Metabolism |
α-Glucosidase-IN-4 是一种有效的α- 葡萄糖苷酶 (α-glucosidase)抑制剂,具有降血压和降糖活性。 | |||
T38654 |
Cotosudil
|
ROCK | Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells |
Cotosudil 是一种 ROCK 激酶抑制剂,具有抗高血压活性,可用于治疗或预防白内障、心血管疾病或神经退行性疾病或神经损伤引起的疾病或病症。 | |||
T1066L |
Ketanserin tartrate
KJK 945 tartrate,KJK-945 tartrate,KJK945 tartrate |
5-HT Receptor; Serotonin Transporter; Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Ketanserin tartrate (KJK-945 tartrate) 是 5-HT2A 受体和α1-肾上腺素能受体拮抗剂,具有抗高血压活性,抑制血清素诱导的血管收缩和血小板活化,可用于研究系统性硬化症。 | |||
T12596 |
(4E)-SUN9221
|
5-HT Receptor; Adrenergic Receptor | GPCR/G Protein; Neuroscience |
(4E)-SUN9221 是一种有效的 α1-adrenergic 受体和 5-HT2 受体双重拮抗剂,在高血压大鼠中显示出抗高血压和抗血小板聚集活性。 | |||
T1439 |
Lacidipine
SN-305,拉西地平,GX-1048,GR-43659X |
Apoptosis; Calcium Channel; Reactive Oxygen Species | Apoptosis; Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism; NF-κB |
Lacidipine (SN-305) 是一种L 型钙离子通道阻断剂。 | |||
T60351 |
Acetazolamide sodium
OT-302 sodium |
Carbonic Anhydrase | Metabolism |
Acetazolamide sodium (OT-302 sodium) 是一种高效的碳酸酐酶 (CA)IX抑制剂,具有利尿、抗淋球菌和降压活性,可用于癫痫、青光眼、水肿和高原反应等适应症。 | |||
T0706 |
Lisinopril dihydrate
Lisinopril,Renacor,赖诺普利二水合物,MK-521 (dihydrate) |
RAAS; MRP | Endocrinology/Hormones; Immunology/Inflammation |
Lisinopril dihydrate (MK-521) 是一种血管紧张素转化酶抑制剂。Lisinopri dihydrate 能够作用于高血压,充血性心力衰竭和心脏病等。 | |||
T0388 |
Cilnidipine
FRC-8653,西尼地平 |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Cilnidipine (FRC-8653) 是二氢吡啶类Ca2+通道阻断剂,可作用于 L 和 N 型 Ca2+通道,具有抗高血压活性。 | |||
T68171 |
Zabicipril
|
RAAS | Endocrinology/Hormones |
Zabicipril 是一种新型可口服的血管紧张转换酶抑制剂,是一种前药,在体内脱酯后具有抗高血压活性。 | |||
T21640 |
Talinolol
|
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Talinolol 是一种长效、心脏选择性的 β1-肾上腺素能受体阻滞剂,具有心脏保护和抗高血压作用。它也是众所周知且经常使用的 P-糖蛋白 (P-gp) 活性探针底物。 | |||
T62893 |
SM-2470
|
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
SM-2470 是一种α1-adrenoceptor拮抗剂,具有降压活性,可减低前神经节肾上腺神经活性和主动脉降压神经活性。SM-2470 具有降胆固醇活性,可抑制胆固醇吸收。 | |||
T0342 |
Carvedilol phosphate hemihydrate
Carvedilol phosphate,BM 14190 (phosphate hemihydrate),卡维地洛磷酸盐 |
VEGFR; Others; Potassium Channel; LDL; Integrin; Gap Junction Protein; NADPH; Adrenergic Receptor; Autophagy | Angiogenesis; Autophagy; Cytoskeletal Signaling; GPCR/G Protein; Membrane transporter/Ion channel; Metabolism; Neuroscience; Others; Tyrosine Kinase/Adaptors |
Carvedilol phosphate hemihydrate (BM 14190 phosphate hemihydrate) 是一种外消旋混合物,是一种非选择性β/α-1受体阻断剂,具有抗高血压活性且缺乏内在拟交感神经活性。 | |||
T7656 |
Apelin-13
|
||
Apelin-13 是存在于中枢和外周神经系统由13个氨基酸组成的多肽序列,是 G 蛋白偶联受体angiotensin II protein J (APJ) 的内源性配体,对 APJ 的 EC50 值为 0.37 nM。Apelin-13 具有扩张血管和降压活性,可用于研究 2 型糖尿病综合征。 | |||
T22368 |
Metyrosine
甲酪氨酸,α-Methyltyrosine |
COX | Immunology/Inflammation; Neuroscience |
Metyrosine (α-Methyltyrosine) 是一种选择性酪氨酸羟化酶抑制剂,可显著抑制高 COX-2 活性和有效控制血压,具有抗炎和抗溃疡作用。 | |||
TNU0187 |
2',5-Difluoro-2'-deoxy-1-arabinosyluracil
2'-Deoxy-2'-fluoro-5-fluoro-arabinouridine |
Nucleoside Antimetabolite/Analog | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
2',5-Difluoro-2'-deoxy-1-arabinosyluracil (2'-Deoxy-2'-fluoro-5-fluoro-arabinouridine) 是一种尿嘧啶核苷类似物,具有潜在的抗癫痫活性和降压活性,可用于研究抗惊厥和焦虑症。 | |||
T16571 |
Pranidipine
普拉地平,OPC-13340 |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Pranidipine (OPC-13340) 是一种高效且长效的 1,4-二氢吡啶钙通道阻滞剂,可延长乙酰胆碱诱导的内皮松弛以及硝酸甘油诱导的内皮松弛,具有抗高血压作用。 | |||
T1282 |
Carteolol hydrochloride
Arteoptic,Abbott-43326,OPC-1085 hydrochloride,盐酸卡替洛尔,Carteolol HCl,Mikelan |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Carteolol hydrochloride (Abbott-43326) 是一种非选择性的β肾上腺素受体阻断剂。 | |||
T1545 |
Levamlodipine
左旋氨氯地平,(S)-Amlodipine,S-amlodipine |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Levamlodipine (S-amlodipine) 是一种二氢吡啶钙通道阻滞剂,具有舒张血管的作用,可用于高血压和心绞痛的研究。 | |||
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。 | |||
T19722 |
Benazeprilat
CGS14831,CGS-14831,CGS 14831 |
RAAS; Endogenous Metabolite | Endocrinology/Hormones; Metabolism |
Benazeprilat(CGS 14831) 是一种具有口服活性的贝那普利活性代谢物。Benazeprilat 具有高效的抗血压活性,可与其他其他类别的化合物(包括噻嗪类利尿剂和钙通道阻滞剂)联合使用来减少与心血管风险和继发性终末器官损伤相关的疾病的发生。Benazeprilat 可能用于研究急性左心室衰竭。 | |||
T68095 |
Losulazine
|
Dopamine Receptor; Norepinephrine | GPCR/G Protein; Neuroscience |
Losulazine 是一种新型的降压化合物。其确切的作用机制尚未确定,但其降压作用取决于完整的、功能性交感神经系统的存在。 | |||
T4284 |
Levamlodipine besylate
左旋氨氯地平,(S)-Amlodipine Besylate (103129-82-4(free base)) |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Levamlodipine besylate ((S)-Amlodipine Besylate(103129-82-4(free base))) 是一种二氢吡啶钙通道阻滞剂,具有舒张血管的作用,可用于高血压和心绞痛的研究。 | |||
T27501 |
Guanoctine hydrochloride
A 7283,A7283,A-7283 |
||
Guanoctine hydrochloride has antihypertensive activity. | |||
T27930 |
LY-127210 free base
LY 127210,LY127210 |
||
LY-127210 free base is peripheral arterial vasodilator with antihypertensive activity. | |||
T27608 |
Indolapril hydrochloride
REV 6000A(SS),CI-907,CI 907,CI907,Indolapril HCl |
||
Indolapril hydrochloride is a nonsulfhydryl angiotensin converting enzyme (ACE) inhibitor with antihypertensive activity. | |||
T28908 |
TA-606
TA-606 free,TA606 |
||
TA-606 is an angiotensin type 1 receptor antagonist with antihypertensive activity. | |||
T12704 |
Rentiapril
SA-446 |
RAAS | Endocrinology/Hormones |
Rentiapril is an orally active inhibitor of angiotensin converting enzyme (ACE), with antihypertensive activity. | |||
T68412 |
Cilazaprilat
|
||
Cilazaprilat is the active metabolite of cilazapril, a pyridazine angiotensin-converting enzyme (ACE) inhibitor with antihypertensive activity. | |||
T74594 |
Tonlamarsen
|
||
Tonlamarsen 是一种血管紧张肽原合成还原剂,具有抗高血压活性。 | |||
T79267 |
Antihypertensive agent 3
|
||
Antihypertensive agent 3 (compound 4a) 是一种针对血管紧张素 II 受体 1(AT1) 的拮抗剂,其在自发性高血压大鼠(SHRs)的模型中表现出显著的降压效果。 | |||
T26452 |
A 80b
A80b,A-80b |
||
A-80b is a synthesized pyridazino[4,5-b]indole derivate with potent and long-lasting antihypertensive activity. The decrease in diastolic pressure was greater than the decrease in systolic pressure and cardiac frequency was not modified significantly. A-8 | |||
T71229 | NA 0346 | ||
NA 0346 is a derivative of SF 2370 that shows long lasting antihypertensive action as well as potent protein kinases inhibitory activity. | |||
T36206 |
Methyldopate
|
||
Methyldopate is an ethyl ester prodrug form of methyldopa , a dopamine decarboxylase inhibitor that has antihypertensive activity in vitro and in vivo., Formulations containing methyldopate have been used in the treatment of hypertension. | |||
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 | |||
T15455 |
RGH-5526
GYKI-11679 |
Others | Others |
RGH-5526是一种新型的抗高血压药。它引起下丘脑去甲肾上腺素(NA)周转(利用)增加,下丘脑去甲肾上腺素能神经元活性的增加可能导致外周交感神经活性的降低,从而显著降低血压。 | |||
T61095 |
SCH-42354
|
||
SCH-42354 is a potent, orally active inhibitor of neutral endopeptidase (NEP), serving as the active form of the prodrug SCH-42495. By inhibiting NEP hydrolysis, SCH-42354 enhances the activity of atrial natriuretic peptide (ANP) and prevents the hydrolysis of leu-enkephalin and ANF with IC50 values of 8.3 nM and 10.0 nM, respectively. Furthermore, SCH-42354 exhibits antihypertensive activity [1] [2]. | |||
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)。 | |||
T36643 |
PKI-166 hydrochloride
|
||
Potent EGFR-kinase inhibitor (IC50 = 0.7 nM). Displays >3000-fold selectivity against a panel of serine/threonine kinases. Reduces metastasis and angiogenesis in a mouse model of pancreatic cancer. Antihypertensive and orally bioavailable. Bruns et al (2000) Blockade of the epidermal growth factor receptor signaling by a novel tyrosine kinase inhibitor leads to apoptosis of endothelial cells and therapy of human pancreatic carcinoma. Cancer Res. 60 2926 PMID:10850439 |Ulu et al (2013) Epidermal ... | |||
T27595 |
Imarikiren HCl
TAK-272 hydrochloride,TAK-272 HCl. Imarikiren HCl |,TAK272,TAK 272,TAK-272 |
||
Imarikiren is a potent, selective and orally active direct renin inhibitor. TAK-272 shows potent inhibitory activity against human renin (IC50 = 2.1 nM) in hPRA assay and excellent selectivity against other aspartic proteases, such as cathepsin D (IC50 > | |||
T35876 |
Chlorthalidone Impurity G
|
||
Chlorthalidone impurity G is a potential impurity found in commercial preparations of chlorthalidone that has moderate antihypertensive effects. Chlorthalidone is a thiazide-like diuretic that inhibits the Na+/Cl- cotransporter in the distal convoluted tubule of the kidney, which prevents reabsorption of sodium and chloride leading to a reduction in plasma volume and cardiac output. It also inhibits carbonic anhydrase (CA), including the isoforms CAVB, VII, IX, XII, and XIII (Kis = 2.8-23 nM) an... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
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。 | |||
T1035 |
Hesperidin
橙皮甙,Hesperetin 7-rutinoside,Cirantin,橙皮苷 |
Apoptosis; Reactive Oxygen Species; Endogenous Metabolite; Autophagy | Apoptosis; Autophagy; Immunology/Inflammation; Metabolism; NF-κB |
Hesperidin (Cirantin) 是一种广泛存在于柑橘类水果中黄烷酮糖苷,具有减少炎症介质并发挥重要的抗氧化作用,还有抗肿瘤和抗过敏活性。 | |||
T0883 |
Tramiprosate
Homotaurine,3-Amino-1-propanesulfonic acid,Alzhemed,高牛黄酸 |
Beta Amyloid; GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
Tramiprosate (Alzhemed) 是一种具有口服活性的、可透过血脑屏障的天然氨基酸,存在于各种红色海藻中,能够可溶性 Aβ 结合并以非原纤维形式维持 Aβ。它是一种 GABA 类似物,具有神经保护,抗惊厥和抗高血压的活性。 | |||
T4S1637 |
gamma-Mangostin
Normangostin,γ-倒捻子素 |
Others; 5-HT Receptor | GPCR/G Protein; Neuroscience; Others |
gamma-Mangostin (Normangostin) 是从药用植物山竹的果壳中提纯的一种天然产物,是一种竞争性5-HT2A 受体拮抗剂。它是运甲状腺素蛋白原纤维化抑制剂,与甲状腺素结合位点结合并稳定了 TTR 四聚体,具有抗高血压、预防结肠癌等作用。 | |||
TN4936 |
Salvisyrianone
|
||
Salvisyrianone 是从台湾隐生植物和叙利亚鼠尾草中分离出二萜,具有潜在的抗高血压活性和抗肿瘤活性。 | |||
TN5645 | Isomartynoside | ||
Isomartynoside has inhibition against the angiotensin converting enzyme (ACE) activities, the IC 50 value is 505±26.7μg/ml, it may have antihypertensive effect. Isomartynoside also shows obvious anti-fatigue activity. | |||
TN4431 |
Leucosceptoside A
|
RAAS; PKC | Chromatin/Epigenetic; Cytoskeletal Signaling; Endocrinology/Hormones |
Leucosceptoside A shows inhibitory activity against PKCalpha with the IC50 value of 19.0 microM; it also exhibits strong inhibitory capacity against α-glucosidase. Leucosceptoside A has antihypertensive effect, it shows angiotensin converting enzyme (ACE) |