55
2
7
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。 | |||
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。 | |||
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。 | |||
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
|
Others | Others |
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
|
Others | Others |
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
T20656 |
Verapamil
NSC 135784,维拉帕米,NSC-135784,CP-16533-1,(±)-Verapamil |
P450; Calcium Channel; P-gp | Membrane transporter/Ion channel; Metabolism; Neuroscience |
Verapamil (CP-16533-1) 是一种非二氢吡啶类钙通道阻滞剂,一种 P-gp 抑制剂,也是一种 CYP3A4 抑制剂,具有口服活性。Verapamil 可以用于治疗高血压、心绞痛、心肌梗塞等。 | |||
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
|
Others | Others |
Watanidipine dihydrochloride is a novel dihydropyridine (DHP)-type calcium channel blocker with slow-onset pharmacological actions. | |||
T0112L2 |
Diltiazem malate
Tiamate,UNII-14Y6444DRP,MK-793 |
Others | Others |
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
|
Others | Others |
Modipaafant is a potent dihydropyridine PAF (platelet activating factor) antagonist. | |||
T68263 |
MDL-72567
|
Others | Others |
MDL-72567 is a dihydropyridine calcium antagonist that causes vasodilation and direct sinus bradycardia. | |||
T70963 |
S 11568
|
Others | Others |
S 11568 is a dihydropyridine calcium channel antagonist. | |||
T17277 | YS-201 | Others | Others |
YS-201 is an antagonist of dihydropyridine-type calcium channel. | |||
T13812 |
PCA50941
|
Others | Others |
PCA50941 is a 1,4-dihydropyridine derivative, treatment for cardiovascular disease. | |||
T34460 |
S 16317
S-16317,S16317 |
Others | Others |
S 16317 is a dihydropyridine derivatives with low calcium channel affinity. | |||
T32997 |
LY 249933
LY249933,LY-249933 |
Others | Others |
LY 249933 is a cardioselective 1, 4-dihydropyridine with positive inotropic activity. | |||
T69157 |
H 160-51
|
Others | Others |
H 160-51 is a calcium agonistic 1,4-dihydropyridine. | |||
T68404 |
Azidopine
|
Others | Others |
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 |
Others | Others |
Levamlodipine gentisate is a pharmacologically active enantiomer of amlodipine. Amlodipine is the dihydropyridine calcium channel blocker used as an antihypertensive and antianginal drug. | |||
T25669 |
Lercanidipine, (S)-
(S)-Lercanidipine,(+)-Lercanidipine |
Others | Others |
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。 | |||
T69001 |
Perindopril arginine
|
Others | Others |
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. | |||
T28321 |
PD 122860
PD-122860,PD122860 |
Others | Others |
PD 122860 is a dihydropyridine with calcium channel blocking and sodium channel stimulating properties. In the rat heart, PD 122860 increased left ventricular contractility, decreased coronary resistance and altered the shape of the electrocardiogram T-wa | |||
T63156 |
SJ000025081
|
Others | Others |
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。 | |||
T39770 |
UK-59811 hydrochloride
|
Others | Others |
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
|
Others | Others |
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 |
---|---|---|---|
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 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。 | |||
T6981 |
Nudifloric 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。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TMIJ-0095 |
Nimodipine-d7
|
||
Nimodipine-d7 是 Nimodipine 的氘代化合物。Nimodipine 的 CAS 号为 66085-59-4。Nimodipine 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。 | |||
TMIJ-0187 |
Lercanidipine-13C-d3 HCl
|
||
Lercanidipine-13C-d3 HCl 是 Lercanidipine HCl 的 13C 和氘代化合物。Lercanidipine HCl 的 CAS 号为 132866-11-6。Lercanidipine hydrochloride 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。 | |||
TMIJ-0140 |
Felodipine-d5
|
||
Felodipine-d5 是 Felodipine 的氘代化合物。Felodipine 的 CAS 号为 72509-76-3。Felodipine 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。 | |||
TMIJ-0077 |
Clevidipine-d7
|
||
Clevidipine-d7 是 Clevidipine 的氘代化合物。Clevidipine 的 CAS 号为 167221-71-8。Clevidipine 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。 | |||
TMIJ-0497 |
Lacidipine-d10
|
||
Lacidipine-d10 是 Lacidipine 的氘代化合物。Lacidipine 的 CAS 号为 103890-78-4。Lacidipine 是一种L型钙离子通道阻断剂。 | |||
TMIH-0087 |
Amlodipine-d4 Maleate (Racemic)
|
||
Amlodipine-d4 Maleate (Racemic) 是 Amlodipine Maleate (Racemic) 的氘代化合物。Amlodipine Maleate (Racemic) 的 CAS 号为 88150-47-4。Amlodipine maleate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。 | |||
TMIJ-0141 |
(S)-Amlodipine-d4
|
||
(S)-Amlodipine-d4 是 (S)-Amlodipine 的氘代化合物。(S)-Amlodipine 的 CAS 号为 103129-82-4。Levamlodipine 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。 |