73
18
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T10900 |
CUDA
|
PPAR; Epoxide Hydrolase | DNA Damage/DNA Repair; Metabolism |
CUDA 是一种可溶性环氧水解酶抑制剂,对小鼠 sEH 和人 sEH 作用的 IC50分别为 11.1 和 112 nM。它能选择性地上调过氧化物酶体增殖激活受体 PPARα的活性,有用于心血管疾病的研究潜力。 | |||
T21957 |
Guanabenz hydrochloride
NE56490 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Guanabenz hydrochloride (NE56490) 是一种具有降血压作用的口服活性 α2-肾上腺素受体激动剂。 | |||
T26923 |
Bunazosin Hydrochloride
E 1015,盐酸布那唑嗪,E643,E-1015,E-643,E 643 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Bunazosin Hydrochloride (E 1015) 是一种 α(1)-adrenoceptor 拮抗剂,用作全身性抗高血压药和降眼压药。 | |||
T28360 |
PF-00489791
PF-4634817,PF 4634817,PF00489791,PF 00489791,PF4634817 |
PDE | Metabolism |
PF-00489791 (PF4634817) 是一种长效 PDE5 抑制剂,具有降血压活性,可用于研究糖尿病肾病。 | |||
T1012 |
Acebutolol hydrochloride
盐酸醋丁洛尔,Acebutolol HCl |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Acebutolol hydrochloride (Acebutolol HCl) 是一种 β-肾上腺素受体拮抗剂,用于研究高血压、心绞痛和心律失常。 | |||
T0028 |
Gamibetal
3-Hydroxy-GABA,4-氨基-3-羟基丁酸,4-Amino-3-hydroxybutyric Acid |
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
Gamibetal (4-Amino-3-hydroxybutyric Acid) 是 γ-氨基-β-羟基丁酸,对癫痫具有潜在的研究价值。 | |||
T24932 |
Vatanidipine
AE-0047,AE 0047,AE0047 |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Vatanidipine (AE0047) 是一种新型的双氢吡啶(DHP)型钙通道阻滞剂,具有缓慢起效的药理作用。在各种实验性高血压模型中观察到缓慢起效和持久的降压作用。 | |||
TP1918L |
Lys-[Des-Arg9]Bradykinin,TFA
Lys-[Des-Arg9]Bradykinin,TFA 71800-36-7(fb-tfa) |
Bradykinin Receptor | GPCR/G Protein |
Lys-[Des-Arg9]Bradykinin,TFA (71800-36-7 free base) 是内源性强效和高选择性的缓激肽 B1 受体激动剂(对人 B1 和 B2 受体的 Ki 值分别为 0.12 和 > 30000 nM)。降低体内外周血管阻力的降压药。比 [Des-Arg9]-缓激肽强 16 倍。 | |||
T22398 |
Phenidone
菲尼酮,1-phenyl-3-pyrazolidinone |
Lipoxygenase; COX | Immunology/Inflammation; Metabolism; Neuroscience |
Phenidone (1-phenyl-3-pyrazolidinone) 是可口服发环氧化酶和脂氧合酶双重抑制剂,可改善实验性自身免疫性脑脊髓炎大鼠的瘫痪,降低自发性高血压大鼠的血压,可用作照片显像剂。 | |||
TP1917L1 |
Sar-[D-Phe8]-des-Arg9-Bradykinin acetate
Sar-[D-Phe8]-des-Arg9-Bradykinin acetate(126959-88-4 free base) |
Bradykinin Receptor | GPCR/G Protein |
Sar-[D-Phe8]-des-Arg9-Bradykinin acetate(126959-88-4 free base) 是一种有效的选择性缓激肽 B1 受体激动剂(兔主动脉中的 EC50 = 9.02 nM),对氨肽酶、激肽酶 I 和 II (ACE) 以及中性内肽酶切割具有抗性。在体内表现出降血压和血管生成活性。 | |||
TP1918L1 |
Lys-[Des-Arg9]Bradykinin acetate
Lys-[Des-Arg9]Bradykinin acetate (71800-36-7 free base) |
Bradykinin Receptor | GPCR/G Protein |
Lys-[Des-Arg9]Bradykinin acetate (71800-36-7 free base) 是一种内源性强效和高选择性的缓激肽 B1 受体激动剂(对人 B1 和 B2 受体的 Ki 值分别为 0.12 和 > 30000 nM)。降低体内外周血管阻力的降压药。比 [Des-Arg9]-缓激肽强 16 倍。 | |||
T1050 |
Prazosin hydrochloride
Prazosin hydrochloride,哌唑嗪盐酸盐,Prazosin HCl,cp-12299-1,Peripress,Vasoflex,盐酸哌唑嗪,Minipress |
Potassium Channel; MRP; Adrenergic Receptor; ABC; Autophagy | Autophagy; GPCR/G Protein; Immunology/Inflammation; Membrane transporter/Ion channel; Neuroscience |
Prazosin hydrochloride (Vasoflex) 是一种选择性肾上腺素能 α-1 拮抗剂,可降低外周阻力并放松血管平滑肌。 它可用于研究高血压和酒精使用障碍。 它是一种合成哌嗪衍生物,具有降压抗肾上腺素能特性。它抑制有机阳离子转运蛋白 OCT-1 和 OCT-3,IC50分别为 1.8 和 13 μM 。 | |||
T0782 |
Benzthiazide
Aquatag,苄噻嗪,Lemazide,Dihydrex |
Carbonic Anhydrase | Metabolism |
Benzthiazide (Lemazide) 是长效利尿剂及抗高血压剂。它也是碳酸酐酶 9 的抑制剂,他对 CA9,CA2 和 CA1 的 Ki 分别为 8.0,8.8 和 10 nM。它对肿瘤细胞增殖具有抑制作用。 | |||
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。 | |||
T34414 |
RS 61565
RS-61565,RS61565 |
||
RS 61565 is a hypotensive agent. | |||
T17113 |
Tolonidine
|
Others | Others |
Tolonidine is orally active and has been shown to possess hypotensive. Tolonidine is a derivative of imidazoline. | |||
T34294 |
Reserpiline
Elliptamine |
||
Reserpiline is a hypotensive extract of Rauwolfia vomitoria. | |||
T26586 |
AL-37350A
|
||
AL-37350A is a 5-HT2 receptor-selective agonist with ocular hypotensive activity. | |||
T13142 |
Theodrenaline
(±)-Theodrenaline,茶碱那林 |
Others | Others |
Theodrenaline is a cardiac stimulant, also acts as an agent of anti-hypotensive together with cafedrine. | |||
T21274 |
Amiquinsin
|
||
Amiquinsin is a drug with hypotensive effect. | |||
T10544 |
Bimatoprost D5
AGN 192024 D5 |
Others | Others |
Bimatoprost (AGN 192024) D5 is a deuterium-labeled Bimatoprost. Bimatoprost is a topical hypotensive agent frequently used for treating glaucoma and ocular hypertension. | |||
T26417 |
A 39355
A39355,A-39355 |
||
A 39355 may specifically overcome multidrug resistance without the serious hypotensive effects associated with calcium antagonists. | |||
T32458 |
L 653328
L 653,328,L653328,L653,328,L-653,328,L-653328 |
||
L 653328 is an ocular hypotensive agent that has modest beta-receptor blocking activity. | |||
T29725 |
AGN-191129
AGN191129,Prostaglandin F2α alcohol methyl ether,PGF2α-OMe,UNII-NK1168QB5T |
||
AGN-191129, also known as Prostaglandin F2α alcohol methyl ether (PGF2α-OMe), is an analog of PGF2α in which the C-1 carboxyl group has been replaced by an O-methyl ether. The compound is reported to retain ocular hypotensive properties, but the receptors | |||
T26426 |
A 62198
A62198,A-62198 |
||
A 62198 is a potent and selective renin inhibitor with potential as a hypotensive agent. | |||
T30452 |
Bimatoprost isopropyl ester
17-phenyl trinor PGF2α-iPr,17-phenyl trinor PGF2α isopropyl ester |
||
Bimatoprost isopropyl ester is an F-series prostaglandin analog, which has been approved as a hypotensive drug. | |||
T68707 | DJ 7141 | ||
DJ 7141 is a unique alpha-2 agonist which shows high affinity to peripheral alpha-2 adrenoceptors but only a mild hypotensive activity. | |||
T37627 |
Latanoprost ethyl amide
|
||
Latanoprost ethyl amide (Lat-NEt) is a latanoprost analog in which the C-1 carboxyl group has been modified to an N-ethyl amide. Prostaglandin esters have been shown to have ocular hypotensive activity. Prostaglandin N-ethyl amides were recently introduced as alternative prostaglandin ocular hypotensive prodrugs. Although it has been claimed that prostaglandin ethyl amides are not converted to the free acids in vivo, studies in our laboratories have shown that bovine and human corneal tissue con... | |||
T68774 |
Deterenol Free Base
|
||
Deterenol Free Base is a beta-adrenoceptor agonist. It is an effective nonmydriatic and nonmiotic hypotensive agent, which can be used in antiglaucoma treatment. | |||
T27754 |
KUL-7211
KUL7211,KUL 7211 |
||
KUL-7211 is an β2 and β3 adrenergic receptor agonist. KUL-7211 is a potent ureteral relaxant with a relatively small hypotensive effect. | |||
T76453 |
Substance P (6-11)
|
||
Substance P (6-11),Substance P 的C末端六肽酰胺,可与NK-1速激肽受体结合,展现出对运动神经元的去极化作用以及降压效应。 | |||
T16711 | Flesinoxan | 5-HT Receptor | GPCR/G Protein; Neuroscience |
Flesinoxan is a hypotensive agent and is an effective, high affinity, and selective 5-hydroxytryptamine1A receptor agonist (EC50: 24 nM). | |||
T39246 |
Brain Natriuretic Peptide-45, mouse
Brain Natriuretic Peptide-45, mouse,BNP-45, mouse |
||
Mouse Brain Natriuretic Peptide-45 (BNP-45, mouse) is a circulating variant of the mouse brain natriuretic peptide derived from the mouse heart. It exhibits powerful hypotensive and natriuretic properties. | |||
T62476 |
Trimazosin
|
||
Trimazosin 是一种口服具有活力的 quinazoline 衍生物,结构与 prazosin 有关。Trimazosin 能够选择性阻断α1肾上腺素受体 (α1-adrenoceptors),具有降压 (hypotensive) 活性。 | |||
T81557 |
PAMP-12(human, porcine) TFA
|
||
PAMP-12(human, porcine) TFA,免疫反应性PAMP(ir-PAMP)的关键成分,源自肾上腺髓质素前体,具有调节心血管功能和显著降压作用的生物活性肽。 | |||
T25568 |
Ketanserinol
Reduced ketanserin |
||
Ketanserinol is the metabolite of ketanserin. Ketanserin is a hypotensive drug with 5-HT2 receptor antagonism, used to reverse pulmonary hypertension caused by protamine. | |||
TP1257 |
Adrenomedullin (AM) (22-52), human
22-52-Adrenomedullin (human) |
||
Adrenomedullin (ADM) is a 52-aa hypotensive peptide. Adrenomedullin (ADM) has structural similarity with amylin. | |||
TP1207 |
Brain Natriuretic Peptide-45, rat
BNP-45 (rat),Brain natriuretic peptide-45 rat |
||
BNP-45 (rat) is a circulating form of rat brain natriuretic peptide isolated from rat heart with potent hypotensive and natriuretic potency. | |||
T37813 |
Fluprostenol methyl ester
|
||
Fluprostenol is an F-series prostaglandin analog which has been approved for many years as a luteolytic in veterinary animals. The isopropyl ester of fluprostenol (travoprost) is an effective ocular hypotensive drug. CAY10532 is a methyl ester analog of fluprostenol. | |||
T62744 |
LpxC-IN-9
|
||
LpxC-IN-9 (compound 19) 是一种 LpxC 的有效抑制剂,表现出抗菌和降血压活性。 | |||
T9819 |
Bunazosin
|
||
Bunazosin 是一种有效的选择性 α1-肾上腺素受体 (α1-adrenoceptor) 拮抗剂,可用于降压和降眼压研究。 | |||
TP1206 |
BNP-45 (rat) (TFA) (123337-89-3 free base)
BNP-45 (rat) (TFA),Brain natriuretic peptide-45 rat TFA |
||
BNP-45 (rat) TFA is a circulating form of rat brain natriuretic peptide isolated from rat heart with potent hypotensive and natriuretic potency. | |||
T38017 | Nω-Propyl-L-arginine hydrochloride | ||
Highly selective and potent inhibitor of nNOS (Ki = 57 nM). Displays 3158-fold and 149-fold selectivity over iNOS and eNOS respectively. Hypotensive in vivo. Kakoki et al (2001) The influence of nitric oxide synthase 1 on blood flow and interstitial nitric oxide in the kidney. Am.J.Physiol.Regul.Integr.Comp.Physiol. 281 R91 PMID:11404282 |Zhang et al (1997) Potent and selective inhibition of neuronal nitric oxide synthase by Nω-propyl-L-arginine. J.Med.Chem. 40 3869 PMID:9397167 | |||
T37213 |
5-trans Latanoprost
|
||
Latanoprost is an F-series prostaglandin analog which has been approved for use as an ocular hypotensive drug. 5-trans Latanoprost is an isomer of latanoprost wherein the double bond between carbons 5 and 6 has been changed from cis (Z) to trans (E). The trans isomer of latanoprost occurs as an impurity of between 2-5% in most commercial preparations of the bulk drug product. The present compound was prepared primarily as an analytical standard for detection and quantitation of this impurity. Fr... | |||
T75084 | Foslevcromakalim | ||
Foslevcromakalim (QLS-101 ) 是一种ATP 敏感的钾通道开启剂。Foslevcromakalim 是用于降眼压作用的前体。 | |||
TP1918 |
Lys-[Des-Arg9]Bradykinin
|
||
Endogenous potent and highly selective bradykinin B1 receptor agonist (Ki values are 0.12 and > 30000 nM at human B1 and B2 receptors respectively). Hypotensive agent that reduces peripheral vascular resistance in vivo. 16-fold more potent than [Des-Arg9] | |||
TP1885 |
[(pF)Phe4]Nociceptin(1-13)NH2
|
||
Highly potent and selective nociceptin/orphanin FQ receptor (OP4) agonist peptide (pKi = 10.68; pEC50 = 9.80). Displays > 8000-fold selectivity over δ, κ, and μ opioid receptors and has relatively long lasting pronociceptive, hypotensive, negative inotrop | |||
T61075 |
Piperilate
|
||
Piperilate, also known as Pipethanate, is a hetrazepine derivative PAF antagonist and anticholinergic mixture, commonly utilized in bronchial asthma research. This compound exhibits hypotensive properties and has been found to effectively counteract the toxic effects of organophosphates in mice [1] [2] [3]. | |||
TP1917 |
Sar-[D-Phe8]-des-Arg9-Bradykinin
|
||
Potent and selective bradykinin B1 receptor agonist (EC50 = 9.02 nM in rabbit aorta) that is resistant to aminopeptidase, kininase I and II (ACE) and neutral endopeptidase cleavage. Exhibits hypotensive and angiogenic activity in vivo. | |||
T37939 |
N-Desethyl Bimatoprost
17-phenyl trinor Prostaglandin F2α amide |
||
N-Desethyl Bimatoprost (17-phenyl trinor PGF2α amide) is an F-series PG analog in which the C-1 carboxyl group has been modified to an unsubstituted amide. PG esters have been shown to have ocular hypotensive activity. PG N-ethyl amides were recently introduced as alternative PG hypotensive prodrugs. Although it has been claimed that PG amides are not converted to the free acids in vivo, studies have shown that bovine and human corneal tissue converts the amides of various PGs to the free acids ... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T13482 |
2'-O-Methyladenosine
|
Endogenous Metabolite | Metabolism |
2'-O-Methyladenosine 是甲基化腺嘌呤的残基,在正常人群和腺苷脱氨基酶缺乏病人的尿液中均可被检测到。它显示出独特的降血压活性。 | |||
T4036 |
Solasodine
Solancarpidine,Purapuridine,澳洲茄铵,Solasodin |
Apoptosis; Others; E1/E2/E3 Enzyme; Antifungal | Apoptosis; Microbiology/Virology; Others; Ubiquitination |
Solasodine (Purapuridine) 是存在于茄科植物中的一种类固醇生物碱。它具有神经保护、降压、抗真菌、抗癌、抗动脉粥样硬化、抗雄激素和抗炎活性。 | |||
T5721 |
Dehydroevodiamine hydrochloride
|
AChE | Neuroscience |
Dehydroevodiamine hydrochloride 是分离自吴茱萸叶中,能够抑制 AChE。 它能够调节一氧化氮的产生,具有降压和神经保护作用。 | |||
TQ0185 |
14-Deoxy-11,12-didehydroandrographolide
AP10,14-脱氧-11,12-二去氢穿心莲内酯,14-dehydro Andrographolide |
NF-κB | NF-κB |
14-Deoxy-11,12-didehydroandrographolide (AP10) 是一种 Andrographolide 的类似物,能够抑制 NF-κB 活性。 | |||
T3013 |
Catharanthine tartrate
Catharanthine hemitartrate,酒石酸长春质碱 |
Others; Calcium Channel | Membrane transporter/Ion channel; Metabolism; Others |
Catharanthine tartrate (Catharanthine hemitartrate) 是长春花中的一种生物碱,可抑制电压门控 L 型钙离子通道,具有抗肿瘤和降血压活性。 | |||
T3S0629 |
Delsoline
Belsoline,硬飞燕草碱 |
Others | Others |
Delsoline (Belsoline) 是一种还亮草的主要生物碱,具有类似箭毒的效果和神经节阻滞作用,可用于肌肉紧张或运动过度的缓解。其中还亮草具有祛风除湿,止痛,活络的功效,可用于风湿,偏瘫,消化不良和咳嗽的研究。 | |||
T2S2335 |
Dehydroevodiamine
DHED,去氢吴茱萸碱 |
Others; NF-κB; COX; PGE Synthase; NO Synthase | Immunology/Inflammation; Neuroscience; NF-κB; Others |
Dehydroevodiamine (DHED) 是从吴茱萸中分离出的一种喹唑啉生物碱,可抑制 LPS 诱导的小鼠巨噬细胞中iNOS、COX-2、PGE2和NF-κB 的表达,对豚鼠心室肌细胞具有抗心律失常作用。 | |||
TN2322 |
Yangambin
|
Calcium Channel; PAFR | GPCR/G Protein; Membrane transporter/Ion channel; Metabolism |
Yangambin 是从诸如番荔枝科植物中分离出来的呋喃木脂素,是选择性PAF 受体拮抗剂,通过调控Ca2+通道抑制 Ca2+流入,导致 [Ca2+]i 在血管平滑肌细胞和随后的外周血管舒张中减少,具有降压作用。 | |||
T8198 |
Visnagin
|
Others | Others |
Visnagin 是一种抗氧化剂呋喃香豆素衍生物。它具有预防Cerulein 诱导的急性胰腺炎的潜力。它在血管平滑肌中具有良好的血管扩张作用。它具有抗炎作用,可用于缓解疼痛的研究。 | |||
T3S1729 |
Dihydrolycorine
|
Others | Others |
Dihydrolycorine 是分离自Lycoris radiate 草药中,是一种真核细胞中蛋白质合成的抑制剂。 | |||
T15824 |
Lysergol
|
Antibacterial | Microbiology/Virology |
Lysergol 已被用作一种降血压、精神镇痛药以及刺激子宫和肠道的药物。 Lysergol 是从 Ipomoea muricata 的种子中分离出来的一种棒状生物碱,是药物和营养物质的生物增强剂,具有抗菌活性。 | |||
T25900 |
Oosponol
Lenzitin |
||
Oosponol is a dopamine beta-hydroxylase inhibitor exhibiting hypotensive effects. | |||
TN2271 |
Thalrugosaminine
|
Antifection | Microbiology/Virology |
Thalrugosaminine shows promising antibacterial activity with MIC values of 64-128ug/ml and Staphylococcus species is the most sensitive strains. Thalrugosaminine possesses hypotensive activity in rabbits and is active against Mycobacterium smegmatis. | |||
TN2990 |
3alpha-dihydrocadambine
|
Others | Others |
3alpha-Dihydrocadambine exhibits dose-dependent hypotensive and anti-hypertensive effects in anesthetized normotensive rats and in conscious spontaneously hypertensive rats. | |||
T4110 |
Perivine
Perivin,派利文碱 |
Others | Others |
Perivine (Perivin) 以视网膜母细胞瘤相关蛋白 (RbAp48) 为靶点,能够解决 RbAp48-FOG-1 复合物的不稳定性。Perivine 可用于研究阿尔茨海默病。 | |||
TN2918 |
3-Acetoxy-8(17),13E-labdadien-15-oic acid
|
cAMP; Potassium Channel; Calcium Channel | GPCR/G Protein; Membrane transporter/Ion channel; Metabolism |
ent-3-Acetoxy-labda-8(17),13-dien-15-oic acid have vasorelaxant and hypotensive actions, the mechanisms underlying the cardiovascular actions of the labdane involve the activation of the endothelial NO-cGMP pathway, the opening of K+ channels and the alteration on Ca2+ mobilization. | |||
TN4652 | Niazimicin | NF-κB; PI3K; AChR; Antifection | Microbiology/Virology; Neuroscience; NF-κB; PI3K/Akt/mTOR signaling |
Niazimicin are NF-B and PI3K inhibitors, which shows antimicrobial, hypotensive and spasmolytic activities. Niazimicin has potent antitumor promoting activity in the two-stage carcinogenesis in mouse skin using 7,12-dimethylbenz(a)anthracene (DMBA) as ini | |||
TN1681 |
Gentianine
|
Others; TNF; transporter; PPAR | Apoptosis; DNA Damage/DNA Repair; Metabolism; Others |
Gentianine 是一种有效的 Swertiamarin 衍生物,具有抗糖尿病、抗精神病、抗炎、降血压、利尿等作用,具有被开发成一种安全的降压药物的潜力。 |