56
2
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T50077 |
m-Nisoldipine
3-methyl 5-(2-methylpropyl) 2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate |
Others | Others |
m-Nisoldipine (3-methyl 5-(2-methylpropyl) 2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate) 是一种二氢吡啶类钙通道阻滞剂,尼索地平的衍生物,阻断心脏和平滑肌细胞中的 L-型钙通道,用于治疗高血压和心绞痛。 | |||
T11074 |
Dolutegravir intermediate-1
1-(2,2-dimethoxyethyl)-5-methoxy-6-methoxycarbonyl-4-oxopyridine-3-carboxylic acid,1-(2,2-dimethoxyethyl)-5-methoxy-6-(methoxycarbonyl)-4-oxo-1,4-dihydropyridine-3-carboxylic acid |
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
Dolutegravir intermediate-1 (1-(2,2-dimethoxyethyl)-5-methoxy-6-(methoxycarbonyl)-4-oxo-1,4-dihydropyridine-3-carboxylic acid) 是 Dolutegravir 的一种新合成中间体。 它是一种整合酶抑制剂,有潜力研究人类免疫缺陷病毒 (HIV)-1 感染。 | |||
T1385 |
Amlodipine
氨氯地平,UK-48340 |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Amlodipine (UK-48340) 是可口服的二氢吡啶钙通道阻滞剂,有抗心绞痛作用。它通过阻断电压依赖性的 L 型钙通道,从而抑制钙离子内流,用于高血压和癌症的研究。 | |||
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。 | |||
T0145 |
Felodipine
非洛地平,CGH-869 |
Calcium Channel; Autophagy | Autophagy; Membrane transporter/Ion channel; Metabolism |
Felodipine (CGH-869) 是一种长效的 1, 4-二氢吡啶钙通道抑制剂,可跨越血脑屏障,可诱导自噬,具有抗高血压活性。它通过选择性作用于血管平滑肌,尤其是阻力血管来降低血压。 | |||
T0231 |
Amlodipine Besylate
Amlodipine benzenesulfonate,苯磺酸氨氯地平 |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Amlodipine Besylate (Amlodipine benzenesulfonate) 是可口服的二氢吡啶钙通道阻滞剂,有抗心绞痛作用。它通过阻断电压依赖性的 L 型钙通道,从而抑制钙离子内流,用于高血压和癌症的研究。 | |||
T0343 |
Nimodipine
尼莫地平,BAY-e 9736 |
Glucocorticoid Receptor; AhR; Calcium Channel; Autophagy | Autophagy; Endocrinology/Hormones; Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism |
Nimodipine (BAY-e 9736) 是一种具有口服活性,耐受性良好的光敏二氢吡啶钙拮抗剂。它可研究脑血管疾病。 | |||
T0957 |
Isradipine
PN 200-110,伊拉地平 |
Calcium Channel; Autophagy | Autophagy; Membrane transporter/Ion channel; Metabolism |
Isradipine (PN 200-110) 是一种二氢吡啶类钙通道阻滞剂,具有抗高血压和血管扩张活性。它是一种具有口服活性的 L 型钙通道阻滞剂,也是一种潜在可行的帕金森病神经保护剂。 | |||
T67592 | 5-(Methoxycarbonyl)-2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylic acid | ||
5-(Methoxycarbonyl)-2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylic acid 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 T67592,CAS号为 74936-72-4。 | |||
T67605 |
4-(2,3-Dichlorophenyl)-5-(methoxycarbonyl)-2,6-dimethyl-1,4-dihydropyridine-3-carboxylic acid
|
||
4-(2,3-Dichlorophenyl)-5-(methoxycarbonyl)-2,6-dimethyl-1,4-dihydropyridine-3-carboxylic acid 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 T67605,CAS号为 123853-39-4。 | |||
T0999 |
Clevidipine
Clevidipine butyrate,丁酸氯维地平,氯维地平,Cleviprex |
Calcium Channel; AChR | Membrane transporter/Ion channel; Metabolism; Neuroscience |
Clevidipine (Clevidipine butyrate) butyrate 是一种二氢吡啶 L 型钙通道阻滞剂,IC50为7.1 nM。它对血管平滑肌有选择性,可用于降低血压。 | |||
T0121 |
Azelnidipine
CS 905,阿折地平,UR-12592 |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Azelnidipine (UR-12592) 是二氢吡啶衍生物,是 L 型钙离子通道阻断剂,有抗高血压作用。 | |||
T15053 |
Darodipine
达罗地平,PY-108068,PY 108-068 |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Darodipine (PY-108068) 是钙离子通道的有效拮抗剂。 | |||
T6227 |
Benidipine hydrochloride
(±)-Benidipine,Benidipine HCl,KW-3049,盐酸贝尼地平,Coniel |
EGFR; Calcium Channel; Src | Angiogenesis; JAK/STAT signaling; Membrane transporter/Ion channel; Metabolism; Tyrosine Kinase/Adaptors |
Benidipine hydrochloride (Coniel) 是二氢吡啶钙通道阻滞剂, 可用于高血压的研究。 | |||
T0163 |
Nisoldipine
尼索地平,BAY-k 5552 |
Calcium Channel; Reactive Oxygen Species | Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism; NF-κB |
Nisoldipine (BAY-k 5552) 是一种高效特异的L 型Cav1.2通道阻断剂,IC50=10 nM。 | |||
T6874 |
Lercanidipine hydrochloride
Corifeo,Carmen,Cardiovasc,乐卡地平盐酸盐,盐酸乐卡地平 |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Lercanidipine hydrochloride (Corifeo) 是亲脂性二氢吡啶-钙通道阻滞剂,具有持久的降压作用和保护肾脏作用。 | |||
T6577 |
Manidipine
Iperten,Franidipine,Artedil,马尼地平 |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Manidipine (Iperten) 是一种二氢吡啶类钙通道阻滞剂,有降压作用。 | |||
T2323 |
Efonidipine
(±)-Efonidipine,NZ-105,依福地平 |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Efonidipine (NZ-105) 是一种二氢吡啶类钙通道阻滞剂,可阻断 T 型和 L 型钙通道。 | |||
T2519 |
Lercanidipine
乐卡地平,Masnidipine |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Lercanidipine (Masnidipine) 是二氢吡啶类的钙通道阻滞剂,具有持久的降压作用和肾脏保护作用。 | |||
T21454 |
Nicardipine
Cardene,Dagan,尼卡地平,Antagonil,Flusemide |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Nicardipine (Cardene) 是一种二氢吡啶类钙通道阻滞剂,可阻断心脏钙通道,IC50为 1 μM,可用于治疗心绞痛和高血压。 | |||
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。 | |||
T21263 |
Amlodipine maleate
Amlodipine (+-)-form maleate,Amvaz |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Amlodipine maleate (Amvaz) 是一种具有口服活性的二氢吡啶类钙通道阻滞剂,通过阻滞电压依赖性 L 型钙通道,从而抑制钙离子内流。Amlodipine maleate 可用于研究高血压和癌症。 | |||
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。 | |||
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。 | |||
T5856 |
Barnidipine hydrochloride
盐酸巴尼地平,YM-09730-5 hydrochloride,Mepirodipine (hydrochloride) |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Barnidipine hydrochloride (YM-09730-5 hydrochloride) 是一种二氢吡啶类钙通道阻滞剂,对 CaA 受体具有选择性作用。它是一种抗高血压药物,通过减少其血管扩张作用继发的外周血管阻力起作用。 | |||
TQ0145 |
(R)-(+)-Bay-K-8644
(R)-(+)-Bay K 8644 |
Calcium Channel; PPAR | DNA Damage/DNA Repair; Membrane transporter/Ion channel; Metabolism |
(R)-(+)-Bay-K-8644 是一种 Ca2+ 通道激动剂,是二氢吡啶激动剂,抑制 Ba2+电流 (IBa),诱导猫的中枢性呼吸抑制,通过竞争性拮抗血栓素 A2-前列腺素 H2 受体抑制血小板活化。 | |||
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。 | |||
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。 | |||
T1146 |
Nifedipine
BAY-a-1040,Procardia XL,Procardia,硝苯地平,Adalat |
CaMK; Potassium Channel; Calcium Channel; Autophagy | Autophagy; Membrane transporter/Ion channel; Metabolism; Neuroscience |
Nifedipine (Procardia) 是一种二氢吡啶类钙通道阻滞剂,可抑制细胞外钙离子跨膜流入心肌和血管平滑肌细胞,导致主要冠状动脉和全身动脉扩张,降低心肌收缩力。它常用于心肌功能不全的相关研究。 | |||
T68123 |
Oxodipine
|
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Oxodipine 是一种二氢吡啶型钙拮抗剂 ,抑制了KCl 诱导的兔主动脉收缩,降低了效力较低的大鼠心室试纸收缩的心脏力量。在大鼠培养的新生儿心室肌细胞中,Oxodipine 降低了L 型Ca 电流(I),IC 为0.24μM,对T 型Ca 电流(I)的IC 为0.41μM。Oxodipine 会使小鼠便秘和狗牙龈增生。 | |||
T23710 | Watanidipine dihydrochloride | ||
Watanidipine dihydrochloride is a novel dihydropyridine (DHP)-type calcium channel blocker with slow-onset pharmacological actions. | |||
T0112L2 |
Diltiazem malate
Tiamate,UNII-14Y6444DRP,MK-793 |
||
Diltiazem malate is an ACE inhibitor and non-dihydropyridine calcium channel blocker used in the treatment of hypertension. | |||
T15733 |
Lemildipine
NB-818,NPK-1886 |
Others | Others |
Lemildipine is a new blocker of dihydropyridine calcium entry. | |||
T33466 | Modipafant | ||
Modipaafant is a potent dihydropyridine PAF (platelet activating factor) antagonist. | |||
T17277 | YS-201 | Others | Others |
YS-201 is an antagonist of dihydropyridine-type calcium channel. | |||
T34460 |
S 16317
S-16317,S16317 |
||
S 16317 is a dihydropyridine derivatives with low calcium channel affinity. | |||
T70963 |
S 11568
|
||
S 11568 is a dihydropyridine calcium channel antagonist. | |||
T32997 |
LY 249933
LY249933,LY-249933 |
||
LY 249933 is a cardioselective 1, 4-dihydropyridine with positive inotropic activity. | |||
T69157 | H 160-51 | ||
H 160-51 is a calcium agonistic 1,4-dihydropyridine. | |||
T13812 |
PCA50941
|
Others | Others |
PCA50941 is a 1,4-dihydropyridine derivative, treatment for cardiovascular disease. | |||
T68263 |
MDL-72567
|
||
MDL-72567 is a dihydropyridine calcium antagonist that causes vasodilation and direct sinus bradycardia. | |||
T68404 |
Azidopine
|
||
Azidopine is a photoactive dihydropyridine channel blocker which may also act as a multidrug resistant (MDR) modulator. | |||
T15021 |
CV-159
|
Others | Others |
CV-159 is a unique dihydropyridine Ca2+ antagonist with antiinflammatory activities. It has an anti-calmodulin (CaM) action. | |||
T25691 |
Levamlodipine gentisate
(S)-Amlodipine gentisate,(S)-(-)-Amlodipine gentisate |
||
Levamlodipine gentisate is a pharmacologically active enantiomer of amlodipine. Amlodipine is the dihydropyridine calcium channel blocker used as an antihypertensive and antianginal drug. | |||
T69001 |
Perindopril arginine
|
||
Perindopril arginine is an angiotensin converting enzyme inhibitor, and amlodipine, a dihydropyridine calcium channel blocker, and is indicated for the treatment of hypertension, to lower blood pressure. | |||
T63156 |
SJ000025081
|
||
SJ000025081 是一种二氢吡啶,能够用做抗疟剂。在小鼠疟疾模型中,SJ000025081 显著抑制 P. yoelii 感染的寄生虫血症。 | |||
T25669 |
Lercanidipine, (S)-
(S)-Lercanidipine,(+)-Lercanidipine |
||
Lercanidipine, (S)-是 Lercanidipine 的异构体,一种降压化合物。Lercanidipine 是二氢吡啶类的钙通道阻滞剂,具有持久的降压作用和肾脏保护作用。 | |||
T0112L |
Diltiazem
Diltiazem free base,Dilticard,地尔硫卓,CRD-401,CRD401,Dilzen,CRD 401 |
||
Diltiazem is a non-dihydropyridine (non-DHP) calcium channel blocker that relaxes the smooth muscle in arterial walls, thus opening (dilating) arteries, allowing easier blood flow, and lowering blood pressure, and is used to treat hypertension, angina pec | |||
T39770 | UK-59811 hydrochloride | ||
UK-59811 hydrochloride is a potent inhibitor of the Ca V Ab voltage-gated calcium channels in bacterial homotetrameric models. It is derived from Br-dihydropyridine, possessing significant inhibitory properties with an IC 50 of 194 nM. | |||
T40345 | AV-153 | ||
AV-153 is a 1,4-dihydropyridine derivative with antimutagenic properties. It intercalates into DNA at single strand breaks, resulting in reduced DNA damage and stimulation of DNA repair in human cells in vitro. AV-153 also interacts with thymine and cytosine and influences poly(ADP)ribosylation. Moreover, AV-153 exhibits anti-cancer activity. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T6981 |
1-Methyl-6-oxo-1,6-dihydropyridine-3-carboxylic acid
1-甲基-6-氧代-1,6-二氢吡啶-3-羧酸,Nudifloric Acid |
Others | Others |
1-Methyl-6-oxo-1,6-dihydropyridine-3-carboxylic acid (Nudifloric Acid) 是来源于冬虫夏草,能够靶向阻断 AP-1 介导的荧光素酶活性,具有抗炎活性。其中冬虫夏草具有抗氧化,抗癌,抗炎,抗糖尿病,抗肥胖,抗血管生成和抗伤害感受活动。 | |||
T8150 |
Nudifloramide
1-Methyl-6-oxo-1,6-dihydropyridine-3-carboxamide,1-甲基-6-氧代吡啶-3-甲酰胺 |
PARP; Endogenous Metabolite | Chromatin/Epigenetic; DNA Damage/DNA Repair; Metabolism |
Nudifloramide (1-Methyl-6-oxo-1,6-dihydropyridine-3-carboxamide) 是烟酰胺-腺嘌呤二核苷酸(NAD) 降解的一种最终产物,可显著抑制PARP-1活性。 |