613
22
4
1
26
Cat. No. | Product Name | ||
---|---|---|---|
L7400 | 钠通道分子库 | 118 compounds | |
118 种钠通道相关化合物的独特集合,可用于高通量筛选和高内涵筛选; | |||
L7300 | 钾通道分子库 | 152 compounds | |
152 种钾通道相关化合物的独特集合,可用于高通量筛选和高内涵筛选; | |||
L5800 | 药物代谢杂质库 | 197 compounds | |
197 种药物异构体/代谢产物的特有集合,可用于高通量、高内涵筛选; | |||
L7110 | 抗高血压化合物库 | 678 compounds | |
678 种高血压相关的小分子,用于高通量和高内涵筛选; |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T11063 |
DMT1 blocker 1
|
Others | Others |
DMT1 blocker 1 是二价金属转运蛋白1 (DMT1) 的阻断剂,IC50 为 0.64 μM,可以阻断体内肠细胞的铁摄取。 | |||
T12504 |
(+)-KCC2 blocker 1
|
Potassium Channel | Membrane transporter/Ion channel |
(+)-KCC2 blocker 1 是 KCC2 的选择性阻断剂 (IC50 = 0.4 μM)。 | |||
T11064 |
DMT1 blocker 2
|
Others | Others |
DMT1 blocker 2 是一种二价金属转运蛋白 1 的直接抑制剂(IC50:0.83 μM)。它可以阻断体内肠细胞的铁摄取。 | |||
T10690 |
Cav 2.2 blocker 1
|
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Cav 2.2 blocker 1 是一种N 型钙离子通道 (Cav 2.2) 的阻断剂,IC50值为 1 nM,可用于治疗疼痛。 | |||
T39717 |
VGSC blocker-1
|
Others | Others |
VGSC blocker-1 is a powerful small molecule that serves as a blocker for the neonatal isoform of the VGSC subtype known as Nav1.5 (nNav1.5). It effectively blocks INa peak currents by 34.9% at a concentration of 1 μM, and demonstrates a 0.3% inhibition of cell invasion at the same concentration in the MDA-MB-231 human breast cancer cell line, without compromising cell viability. | |||
T28132 |
NaV1.7 Blocker-801
|
Others | Others |
NaV1.7 Blocker-801 is a potent NaV1.7 blocker. | |||
T69387 |
NMO-IgG blocker A-01
|
Others | Others |
NMO-IgG blocker A-01 is a idiotype-specific blocker of neuromyelitis opticaimmunoglobulin g (nmo-igg) binding to aquaporin-4 (aqp4) | |||
T72170 |
NaV1.2/1.6 channel blocker-1
|
Sodium Channel | Membrane transporter/Ion channel |
NaV1.2/1.6 channel blocker-1 是一种有效的 NaV1.2/1.6 channel 阻滞剂,对 rNaV1.6 和 hNaV1.2 有抑制作用。NaV1.2/1.6 channel blocker-1 可用于研究全身性癫痫和运动障碍。 | |||
T11927 |
M2 ion channel blocker
|
Others | Others |
M2 ion channel blocker ,Antiviral agent, is capable of inhibiting and blocking the activity of M2 ion channel. | |||
T12153 |
N-type calcium channel blocker-1
|
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
N-type calcium channel blocker-1 is an orally active analgesic agent,shows high affinity to functionally block N-type calcium channels. | |||
T84918 |
MTDH-SND1 blocker 1
C26-A6 |
Others | Others |
MTDH-SND1 blocker 1 (compound C26-A6) 是MTDH-SND1蛋白的抑制剂,可抑制癌症的转移。 | |||
T80930 |
TRPV2-selective blocker 1
|
Others | Others |
TRPV2-selective blocker 1 (compound IV2-1) 为选择性TRPV2通道阻断剂,具有6.3 μM IC50,不对TRPV1、TRPV3和TRPV4通道产生影响。该化合物能够抑制巨噬细胞中TRPV2介导的Ca2+流入,进而抑制其吞噬功能。 | |||
T84901 |
BAI1 hydrochloride
BAI1, BAI 1, BAI-1, Bax channel blocker |
Others | Others |
BAI1 hydrochloride 是选择性凋亡因子BAX变构抑制剂,通过结合BAX并变构抑制其激活,显示出用于研究BAX依赖性细胞死亡介导疾病的潜力。 | |||
T62586 |
Cav 2.2/3.2 blocker 1
|
Others | Others |
Cav 2.2/3.2 blocker 1 (Compound 9e) 是一种神经钙离子通道 (neuronal calcium channel) 阻断剂,能够作用于 Cav2.2 (IC50: 1.22 μM) 和 Cav3.2 (IC50: 80 μM)。Cav 2.2/3.2 blocker 1 可以穿透中枢神经系统。 | |||
T26817 |
Bim-BLK-A
Bim Blocker A,Compound A,Bim BLK A,BimBLKA |
Others | Others |
Bim-BLK-A efficiently blocks Bim-induced apoptosis after Bax is activated on the mitochondria. The cellular target of Bim-BLK-A was identified to be the succinate dehydrogenase subunit B (SDHB) protein of complex II of the mitochondrial electron transfer | |||
T83705 |
BING TFA
Blocker of Inter-membrane Stress Responses of Gram-negative Bacteria |
||
BING是一种来源于日本稻田鱼(O. laptipes)的抗菌肽,由液泡蛋白质分选相关蛋白13D样(Vps13D)衍生而来。对包括耐甲氧西林的金黄色葡萄球菌(MRSA; MICs = 4-64 µg/ml)在内的各种革兰氏阴性和革兰氏阳性细菌都有活性。与氨苄西林、阿莫西林和新霉素共同使用时,对抗铜绿假单胞菌(P. aeruginosa)表现出协同效应,并能抑制大肠杆菌(E. coli)对卡那霉素和氨苄西林的抗药性发展。在体内,BING提高了被鳗弧菌(E. tarda)感染的O. laptipes的生存率。 | |||
T15385 |
Glibornuride
|
Potassium Channel | Membrane transporter/Ion channel |
Glibornuride 是对 ATP 敏感的 K+通道 (KATP 通道) 阻滞剂,pKi 为 5.75。Glibornuride 显示抗糖尿病活性。 | |||
T0440 |
Oxcarbazepine
GP 47680,奥卡西平 |
Apoptosis; Sodium Channel | Apoptosis; Membrane transporter/Ion channel |
Oxcarbazepine (GP 47680) 是一种钠通道阻滞剂,有效抑制胶质母细胞瘤细胞生长并诱导胶质母细胞瘤细胞凋亡或 G2/M 停滞,具有抗癌和抗惊厥作用。 | |||
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。 | |||
T7806 |
Licarbazepine
10,11-hydroxy-10,11 Dihydrocarbamezer,10,11-二氢-10-羟基卡马西平 |
Others | Others |
Licarbazepine (10,11-hydroxy-10,11 Dihydrocarbamezer) 是一种有效的电压门控钠通道阻滞剂,具有抗惊厥和稳定情绪的功效。 | |||
T3574 |
Sematilide hydrochloride
司美利特,CK-1752A,CK-1752,Sematilide HCl |
Potassium Channel | Membrane transporter/Ion channel |
Sematilide hydrochloride (CK-1752) 是一种选择性的 IKr 通道阻滞剂。Sematilide 以浓度依赖性抑制延迟整流钾通道 (K+current),IC50为 25 μM。Sematilide 是一种 III 类抗心律不齐剂。 | |||
T8388 |
Vonoprazan
TAK-438 (free base),沃诺拉赞 |
Proton pump | Membrane transporter/Ion channel |
Vonoprazan (TAK-438 (free base)) 是一种质子泵抑制剂,是口服活性钾竞争性酸阻断剂,有抗分泌作用。在 pH 为 6.5 时,它抑制猪胃微粒体中的 H+,K+-ATPase 酶活性,IC50值为 19 nM。它可用于研究胃酸相关疾病。 | |||
T0866 |
Propafenone
Rythmol,普罗帕酮,Propafenonum |
Potassium Channel; MRP; Sodium Channel | Immunology/Inflammation; Membrane transporter/Ion channel |
Propafenone (Propafenonum) 是钠通道阻滞剂,它对 β 受体具有高亲和力 (IC50=32 nM)。它能够阻断瞬时外向钾电流 (Ito) (IC50: 4.9 nM) 和持续延迟整流器K+电流 (Isus) (IC50: 8.6 nM) ,具有抗心律失常的作用。它能够诱导线粒体功能障碍及诱导细胞凋亡,从而抑制食管癌增殖。 | |||
T21254 |
Vonoprazan Fumarate
TAK-438,TAK 438,Vonoprazan Fumurate,TAK438,富马酸沃诺拉赞 |
Proton pump | Membrane transporter/Ion channel |
Vonoprazan Fumarate (TAK438) 是质子泵的有效抑制剂,是口服有效的高效钾竞争性酸阻断剂,具有抗分泌活性。在 pH 为 6.5 时,它抑制猪胃微粒体中的 H+,K+-ATPase 酶活性,IC50为 19 nM。它被开发用于研究酸相关疾病,如消化性溃疡和胃食管反流病。 | |||
T1615 |
Irbesartan
厄贝沙坦,SR-47436,BMS-186295 |
Apoptosis; RAAS | Apoptosis; Endocrinology/Hormones |
Irbesartan (SR-47436) 是一种 1 型血管紧张素 II 受体拮抗剂,IC50为1.3 nM。 | |||
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。 | |||
T1215 |
Nicardipine hydrochloride
盐酸尼卡地平,RS-69216,Nicardipine HCl,YC-93 Hydrochloride |
Calcium Channel; Adrenergic Receptor; AChR; Autophagy | Autophagy; GPCR/G Protein; Membrane transporter/Ion channel; Metabolism; Neuroscience |
Nicardipine hydrochloride (YC-93 Hydrochloride) 是一种钙通道阻滞剂,IC50为 1 μM。它可阻断某些细胞壁中的钙离子并抑制冠状动脉和外周动脉的收缩,从而降低对氧气的需求心肌和减少动脉收缩和痉挛。它在临床上用作脑和冠状血管扩张剂。 | |||
T3280 |
Clodronate disodium tetrahydrate
clodronic acid disodium tetrahydrate,Disodium clodronate tetrahydrate,Clastoban,氯屈膦酸二钠(四水合物),Clodronate disodium |
IL Receptor; TNF | Apoptosis; Immunology/Inflammation |
Clodronate disodium tetrahydrate (Clastoban) 是一种选择性、高效的,可逆、Cl-竞争性的囊泡核苷酸转运体阻滞剂(IC50:15.6 nM)。是一种双膦酸盐,具有抗骨质疏松、抗炎作用,可用于缓解疼痛的研究。它可抑制神经元释放囊泡 ATP,缓解慢性神经病理性疼痛和炎症性疼痛。 | |||
T6666 |
Sevelamer Carbonate
|
Others | Others |
Sevelamer carbonate 是一种口服具有活力的非钙基磷酸盐结合剂,能有效降低体内血清磷水平,但对体内血清钙、氯水平影响极小,可用于研究慢性肾脏病的高磷血症。它被认为是七氟乙烯的一种改进的缓冲形式。 | |||
T22330 |
Fenamic acid
N-苯基邻氨基苯甲酸,2-Anilinobenzoic acid,Diphenylamine-2-carboxylic acid,2-(Phenylamino)benzoic acid,N-Phenylanthranilic acid |
Chloride channel | Membrane transporter/Ion channel |
Fenamic acid (N-Phenylanthranilic acid) 是氯通道阻滞剂。 | |||
T26081 |
Ridazolol
Ridazololum |
Others | Others |
Ridazolol is a vasodilating and cardioselective beta adrenergic blocker. | |||
T26689 |
AVE-0118
AVE 0118,AVE0118 |
Potassium Channel | Membrane transporter/Ion channel |
AVE-0118 是一种钾通道阻滞剂,可抑制持续性心房颤动。 | |||
T29050 |
UK 66914
UK66914,UK-66914 |
Potassium Channel | Membrane transporter/Ion channel |
UK 66914 是一种 K(+)通道阻断剂,可用于研究心律失常。 | |||
T10813 |
Cilobradine hydrochloride
DK-AH 269 |
HCN Channel | Membrane transporter/Ion channel |
Cilobradine hydrochloride (DK-AH 269) 是一种 HCN 通道阻断剂。 | |||
T20341 |
DNDS
|
CFTR | Membrane transporter/Ion channel |
DNDS 是电压依赖性囊性纤维化跨膜电导调节剂 (CFTR) 的通道阻滞剂。 | |||
T22675 |
Co 102862
V 102862 |
Others; Sodium Channel | Membrane transporter/Ion channel; Others |
Co 102862 是一种电压门控钠通道阻滞剂。 Co 102862 可用于抗惊厥的研究。 | |||
T24661 |
Pridefine
AHR-1118 free base,Pridefina |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Pridefine (Pridefina) 是一种吡咯烷衍生物,是儿茶酚胺和血清素的再摄取阻断剂,具有抗抑郁活性。 | |||
T79835 |
Aneratrigine hydrochloride
|
Sodium Channel | Membrane transporter/Ion channel |
Aneratrigine hydrochloride 是一种钠通道蛋白9型亚基阻断剂,可用于预防或治疗钠通道阻断剂相关疾病。 | |||
T22745 |
DPO-1
|
Potassium Channel | Membrane transporter/Ion channel |
DPO-1 可以高效抑制电压门控钾离子通道Kv1.5,也可以阻断超快速延迟整流钾电流。它能够预防房性心律失常。 | |||
T3557 |
GAL-021
GAL 021 |
Potassium Channel | Membrane transporter/Ion channel |
GAL-021新型静脉内BKCa-channel 阻滞剂。 | |||
T0327 |
Fendiline hydrochloride
Fendiline HCl,盐酸芬他林 |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Fendiline hydrochloride (Fendiline HCl) 是一种非选择性钙通道抑制剂。 | |||
T12385 |
PD0176078
PD176078 |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
PD0176078 () 是一种新型的 N 型钙通道 (Calcium channel) 阻滞剂。 | |||
T7638 |
NPPB
|
Chloride channel | Membrane transporter/Ion channel |
NPPB 是外向整流氯化物通道阻断剂,IC50 为 80 nM。 | |||
T3703 |
ABT-639
ABT 639 |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
ABT-639 是一种有效的选择性 T 型钙通道阻滞剂。 | |||
T23471 |
TRAM 39
2-Chloro-alpha,alpha-diphenylbenzeneacetonitrile,TRAM-39,ZINC27105797,2-(2-chlorophenyl)-2,2-diphenylacetonitrile |
Potassium Channel | Membrane transporter/Ion channel |
TRAM 39 (2-Chloro-α,α-diphenylbenzeneacetonitrile)是一种选择性的中间传导性钙离子激活的K+通道的阻断剂。 | |||
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。 | |||
T7182 |
Metaflumizone
BAS-320I,氰氟虫腙 |
Sodium Channel; Parasite | Membrane transporter/Ion channel; Microbiology/Virology |
Metaflumizone (BAS-320I) 是一种缩氨基脲杀虫剂,是钠离子通道阻滞剂。 | |||
T31716 |
Etidocaine Hydrochloride
W-19053,Duranest,W19053,W 19053 |
Sodium Channel | Membrane transporter/Ion channel |
Etidocaine Hydrochloride (W19053) 是一种长效麻醉剂和电压门控钠通道阻滞剂。 | |||
T12108 |
MRS1845
|
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
MRS1845 是一种 ORAI1 抑制剂和钙进入 (SOCE) 阻滞剂,可阻断VP 诱导的 SOCE、OS 和 Ca(2+) 沉积。 | |||
T15143 |
DMP-543
XR-543 |
Others; Potassium Channel | Membrane transporter/Ion channel; Others |
DMP-543 (XR-543) 是一种钾离子通道 (KV7 channel) 阻滞剂。DMP-543可以增强神经递质的释放。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T3S0081 |
Oxypeucedanin
(+-)-Oxypeucedanin,氧化前胡素,Oxypeucadanin |
Potassium Channel | Membrane transporter/Ion channel |
Oxypeucedanin ((+-)-Oxypeucedanin) 是呋喃香豆素衍生物,分离自Angelica dahurica。它是选择性开放通道阻滞剂,可抑制hKv1.5通道电流,IC50值为 76 nM。它延长心脏动作电位持续时间,是潜在的抗心律失常试剂。它通过抑制癌细胞迁移来诱导细胞凋亡。 | |||
T3054 |
Daurisoline
蝙蝠葛苏林碱,(R,R)-Daurisoline |
Others; Potassium Channel; Autophagy | Autophagy; Membrane transporter/Ion channel; Others |
Daurisoline ((R,R)-Daurisoline) 是一种 hERG 抑制剂,也是一种自噬阻滞剂。 | |||
T23107 |
Ononetin
芒柄花酚,2',4'-Dihydroxy-2-(4-methoxyphenyl)acetophenone |
TRP/TRPV Channel | Membrane transporter/Ion channel |
Ononetin (2',4'-Dihydroxy-2-(4-methoxyphenyl)acetophenone) 是天然脱氧安息香素,是有效的TRPM3 通道选择性阻断剂,IC50为 0.3 μM。 | |||
T6S0084 |
Tuberostemonine
对叶百部碱,Tuberstemonine |
Parasite | Microbiology/Virology |
Tuberostemonine (Tuberstemonine) 是一种生物碱,可作为抗疟疾剂,有较高的肠道通透性。 | |||
T0792 |
(-)-Sparteine sulfate pentahydrate
(-)-Sparteine Sulfate,Lupinidine sulfate pentahydrate,(-)-Sparteine sulfate salt,sulfate pentahydrate,五水合硫酸司巴丁 |
Sodium Channel | Membrane transporter/Ion channel |
(-)-Sparteine sulfate pentahydrate ((-)-Sparteine Sulfate) 是一种生物碱,是钠通道抑制剂,属于1a 类抗心律失常药。 | |||
T0801 |
Tannic acid
单宁酸,Gallotannic acid |
Potassium Channel; HER; CXCR | Angiogenesis; Autophagy; GPCR/G Protein; Immunology/Inflammation; JAK/STAT signaling; Membrane transporter/Ion channel; Tyrosine Kinase/Adaptors |
Tannic acid (Gallotannic acid) 属于多酚类天然产物,是一种 hERG 通道阻塞剂,也是一种 CXCL12/CXCR4 抑制剂。Tannic acid 具有抗菌、抗氧化、抗炎和抗肿瘤等多种生物活性。 | |||
T6631 |
Quinine hydrochloride dihydrate
奎宁单盐酸盐二水合物,Quinine HCl Dihydrate,奎宁盐酸盐二水合物 |
Potassium Channel; Parasite | Membrane transporter/Ion channel; Microbiology/Virology |
Quinine hydrochloride dihydrate (Quinine HCl Dihydrate) 是一种白色结晶 K+ 通道阻滞剂,用于治疗疟疾,具有退热,抗疟,止痛,抗炎等特性。 | |||
T16535 |
Picrotoxinin
|
Chloride channel; GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
Picrotoxinin 是一种氯离子通道阻断剂和 GABAA 的非竞争性拮抗剂,对 α1β2γ2L GABAA 的 IC50 为 1.15 μM。 Picrotoxinin 具有惊厥作用。 | |||
T3S0807 |
Berbamine
|
CaMK; NF-κB; Autophagy | Autophagy; Neuroscience; NF-κB |
Berbamine 是从黄柏中提取的一种天然产物,是钙通道阻滞剂,具有抗肿瘤、免疫调节和心血管作用。 | |||
T7853 |
(+)-Sparteine
鹰爪豆碱,(+)-鹰爪豆碱,Pachycarpine |
AChR | Neuroscience |
(+)-Sparteine (Pachycarpine) 是从苏格兰扫帚中提取的一种生物碱,是钠通道阻滞剂和 1a 类抗心律失常剂。它在神经细胞中竞争性地抑制烟碱型乙酰胆碱受体活性,是神经节阻滞剂。 | |||
T4822 |
N-Acetylglycine
N-乙酰甘氨酸,Acetamidoacetic acid,Aceturic acid |
Others; Endogenous Metabolite | Metabolism; Others |
N-Acetylglycine 是一种食物中的少量成分,无基因毒性和急性毒性,能够用于模拟肽的生物研究。N-Acetylglycine 可充当一种多肽的 N 端的阻断剂。 | |||
T8716 |
physalin F
酸浆苦味素F,酸浆苦素 F |
Apoptosis | Apoptosis |
Physalin F 是一种分泌型甾体,诱导人外周血单个核细胞凋亡,降低人 T 淋巴细胞 1 型病毒感染后的自发增殖和细胞因子的产生,具有强烈抗炎和免疫调节作用。 | |||
TMA2106 |
(-)-Sparteine
|
P450 | Metabolism |
Sparteine is a class 1a antiarrhythmic agent, a sodium channel blocker. The deficient debrisoquine hydroxylation of Sparteine is due to the absence of P-450IID1 protein in the livers of poor metabolizers. | |||
T27191 |
D-Mannuronic Acid
|
||
D-Mannuronic Acid is a blocker of the TLR2 and TLR4 downstream signaling pathway. D-Mannuronic Acid effectively inhibits mRNA expression of MyD88 and p65, major subunit of nuclear factor-kappaB. | |||
T3029 |
Sparteine sulfate
硫酸司巴丁,Depasan,Tocosimplex,Actospar |
Others; Sodium Channel | Membrane transporter/Ion channel; Others |
Sparteine sulfate (Tocosimplex) 是一种 1a 类抗心律失常药和钠通道阻滞剂。它可以螯合二价钙和镁。 | |||
T62265 |
(+)-Sparteine sulfate pentahydrate
|
Others | Others |
(+)-sparteine (sulfate pentahydrate) 是一种神经节阻断剂,可以竞争性阻断神经元中烟碱乙酰胆碱受体。 | |||
TN3636 |
Chlorahololide C
|
Potassium Channel | Membrane transporter/Ion channel |
Chlorahololide C is a potent and selective potassium channel blocker, it exerts potent and selective inhibition on the delayed rectifier (I(K)) K(+) current with the IC(50) value of 3.6 +/- 10.1 mu M. | |||
T75722 |
Chlorotoxin TFA
|
Others | Others |
Chlorotoxin TFA,一种从蝎子毒液中分离出的多肽,作为氯离子通道 (chloride channel) 的阻断剂,具备抗癌活性。 | |||
T21266 |
Quinine sulfate
|
Others | Others |
Quinidine sulfate 是一种抗心律失常剂。Quinidine sulfate 是一种口服有效的、选择性的细胞色素 P450db (cytochrome P450db) 抑制剂。Quinidine sulfate 是 K+通道 (K+channel) 的有效阻断剂,IC50值为 19.9 μM。Quinidine sulfate 同时具有抗疟疾的研究潜力。 | |||
TN3587 |
Capillarisin
|
MMP; ERK; IL Receptor; BCL; VEGFR; TNF; NOS; NF-κB; TLR; MAPK; COX; DNA/RNA Synthesis; Prostaglandin Receptor; JNK; STAT | Angiogenesis; Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; GPCR/G Protein; Immunology/Inflammation; JAK/STAT signaling; MAPK; Neuroscience; NF-κB; Proteases/Proteasome; Stem Cells; Tyrosine Kinase/Adaptors |
Capillarisin is a novel blocker of STAT3 activation and thus may have a potential in negative regulation of growth, metastasis, and chemoresistance of tumor cells, it inhibits cancer cell growth of osteosarcoma cells by inducing apoptosis accompanied with | |||
TN5061 |
Stephanine
|
Adrenergic Receptor; Antifection | GPCR/G Protein; Microbiology/Virology; Neuroscience |
l-Stephanine is a potent and highly selective alpha 1 adrenoceptor blocker, inhibits anococcygeus muscle contraction induced by phenylephrine with pA2 values of 6.76. Stephanine shows significant antiplasmodial activities with IC(50) ranged from 1.2 uM to 52.3 uM. Stephanine and crebanine have high inhibitory activity against gram-positive animal pathogenic bacteria, with MIC values of 0.078-0.312g/l, but low inhibitory activity against gram-negative animal pathogenic bacteria, they also inhibit... | |||
T75697 |
1-Methyl-2-[(4Z,7Z)-4,7-tridecadienyl]-4(1H)-quinolone
|
Others | Others |
1-Methyl-2-[(4Z,7Z)-4,7-tridecadienyl]-4(1H)-quinolone,为喹诺酮类生物碱,作用为二酰基甘油酰基转移酶抑制剂与血管紧张素II受体阻断剂,其IC50值依次为20.1 μM与34.1 μM。此化合物亦展现对幽门螺杆菌的有效抗活性,MIC值达10 μg/mL。 |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPH-03750 |
SLC7A11 Protein, Human, Recombinant (His)
SLC7A11,Calcium channel blocker resistance protein ... |
Human | E. coli |
Sodium-independent, high-affinity exchange of anionic amino acids with high specificity for anionic form of cystine and glutamate. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T12167 |
Nadolol-d9
纳多洛尔 D9,SQ-11725 D9,Nadolol D9 |
Others | Others |
Nadolol D9 is the deuterium labeled Nadolol is a blocker of non-selective beta. | |||
T10439 |
Azelnidipine D7
CS-905 D7 |
Others | Others |
Azelnidipine D7 is a deuterium-labeled Azelnidipine. Azelnidipine is an L-type calcium channel blocker. | |||
T12023 |
Mexiletine-d6 hydrochloride
KOE-1173 D6 hydrochloride,Mexiletine D6 hydrochloride |
Others | Others |
Mexiletine D6 hydrochloride is a non-selective voltage-gated sodium channel blocker,is a Class IB antianhythmic. | |||
T12222 |
Nifedipine-d6
硝苯地平 D6,Nifedipine D6,BAY-a-1040 D6 |
Others | Others |
Nifedipine D6 is deuterium labeled nifedipine which is a potent blocker of calcium channel. | |||
T12625 |
(R)-Lercanidipine-d3 hydrochloride
(R)-Lercanidipine D3 hydrochloride |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
(R)-lercanidipine D3 hydrochloride is a deuterium labeled (R)-Lercanidipine hydrochloride. (R)-Lercanidipine D3 (hydrochloride) is a calcium channel blocker. | |||
T10842 |
Clomipramine D3
氯米帕明 D3 |
Others | Others |
Clomipramine D3 is the deuterium-labeled Clomipramine. Clomipramine is a serotonin transporter, norepinephrine transporter dopamine transporter blocker (Ki: 0.14, 54 and 3 nM). | |||
T13204 |
Trimethobenzamide D6
|
Others | Others |
Trimethobenzamide D6 is deuterium labeled Trimethobenzamide. Trimethobenzamide is a the D2 receptor blocker. Trimethobenzamide is an antiemetic. | |||
T10816 |
Cinnarizine D8
|
Others | Others |
Cinnarizine D8 is a deuterium-labeled Cinnarizine which is an antihistamine and a calcium channel blocker. | |||
T10842L |
Clomipramine D3 hydrochloride
|
Others | Others |
Clomipramine D3 hydrochloride is the deuterium-labeled Clomipramine. Clomipramine is a serotonin transporter, norepinephrine transporter dopamine transporter blocker (Ki: 0.14, 54 and 3 nM). | |||
T12243 |
Norverapamil-d7
D591 D7,(±)-Norverapamil D7 |
Others | Others |
Norverapamil D7 is a deuterium labeled Norverapamil . Norverapamil is a blocker of L-type calcium channel and an inhibitor of P-glycoprotein (P-gp) function . | |||
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-0185 |
Telmisartan-13C-d3
|
||
Telmisartan-13C-d3 是 Telmisartan 的 13C 和氘代化合物。Telmisartan 的 CAS 号为 144701-48-4。Telmisartan 是一种血管紧张素II 1型受体拮抗剂,能够抑制其活性,IC50值为 9.2 nM。 | |||
TMID-0295 |
Fosphenytoin Sodium-d10
|
||
Fosphenytoin Sodium-d10 是 Fosphenytoin Sodium 的氘代化合物。Fosphenytoin Sodium 的 CAS 号为 92134-98-0。Fosphenytoin sodium 是 phenytoin 的前体药物,具有抗惊厥等活性。它是电压门控钠通道阻滞剂。 | |||
TMIH-0107 |
Barnidipine-d5
|
||
Barnidipine-d5 是 Barnidipine 的氘代化合物。Barnidipine 的 CAS 号为 104713-75-9。Barnidipine 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。 | |||
TMIJ-0285 |
Verapamil-d7 Hydrochloride
|
||
Verapamil-d7 Hydrochloride 是 Verapamil Hydrochloride 的氘代化合物。Verapamil Hydrochloride 的 CAS 号为 152-11-4。Verapamil hydrochloride 是一种钙通道阻滞剂,是一种可口服的 P 糖蛋白 (P-gp) 抑制剂,可抑制CYP3A4,用于高血压、心律不齐和心绞痛的研究。 | |||
TMIJ-0270 |
Pinaverium-d4 Bromide (Mixture of Diastereomers)
|
||
Pinaverium-d4 Bromide (Mixture of Diastereomers) 是 Pinaverium Bromide 的氘代化合物。Pinaverium Bromide 的 CAS 号为 53251-94-8。Pinaverium bromide 是一种具有解痉作用的钙通道阻滞剂,可有效缓解疼痛、腹泻和肠道不适。 | |||
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。 | |||
TMIH-0399 |
Norverapamil-d7 HCl
|
||
Norverapamil-d7 HCl 是 Norverapamil HCl 的氘代化合物。Norverapamil HCl 的 CAS 号为 67812-42-4。Norverapamil hydrochloride是 Verapamil 的 N-去甲基代谢物,是L型钙通道阻滞剂和 P-糖蛋白 (P-gp) 功能抑制剂。 | |||
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。 | |||
TMID-0198 |
Esmolol-d7 HCl
|
||
Esmolol-d7 HCl 是 Esmolol HCl 的氘代化合物。Esmolol HCl 的 CAS 号为 81161-17-3。Esmolol hydrochloride 是一种心脏选择性β受体阻滞剂,用于治疗心律失常和严重高血压。 | |||
TMIJ-0131 |
rac-Valsartan-d9
|
||
rac-Valsartan-d9 是 rac-Valsartan 的氘代化合物。rac-Valsartan 的 CAS 号为 137862-53-4。Valsarta 是一种血管紧张素 II 受体拮抗剂,有用于高血压和心力衰竭的研究潜力。 | |||
TMIH-0183 |
Dequalinium Chloride-d4
|
||
Dequalinium Chloride-d4 是 Dequalinium Chloride 的氘代化合物。Dequalinium Chloride 的 CAS 号为 522-51-0。Dequalinium chloride 是一种apamin敏感型的钾离子通道选择性阻断剂。 | |||
TMIH-0002 |
(+/-)-Verapamil hydrochloride-d7
|
||
(+/-)-Verapamil hydrochloride-d7 是 (+/-)-Verapamil hydrochloride 的氘代化合物。(+/-)-Verapamil hydrochloride 的 CAS 号为 152-11-4。Verapamil hydrochloride 是一种钙通道阻滞剂,是一种可口服的 P 糖蛋白 (P-gp) 抑制剂,可抑制CYP3A4,用于高血压、心律不齐和心绞痛的研究。 | |||
TMIJ-0042 |
Metoprolol-d7 Hydrochloride
|
||
Metoprolol-d7 Hydrochloride 是 Metoprolol Hydrochloride 的氘代化合物。Metoprolol Hydrochloride 的 CAS 号为 56392-18-8。Metoprolol 是一种选择性 β1 受体阻滞剂。Metoprolol 用于治疗高血压、因心脏血流不畅而引起的胸痛以及许多心率异常快的疾病。 | |||
TMID-0245 |
Pindolol-d7
|
||
Pindolol-d7 是 Pindolol 的氘代化合物。Pindolol 的 CAS 号为 13523-86-9。Pindolol 是一种非选择性β-阻断剂,局部的β-肾上腺素能受体激动剂活性,也作为5-HT1A受体部分拮抗剂,Ki为33nM。它是非心脏选择性的,具有内在的拟交感神经作用。 | |||
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。 |