Metabolism
Metabolism(代谢)
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Metabolism 相关产品(3072)
- GC15222Siramesine hydrochlorideCAS: 224177-60-0纯度: >99.50%
Siramesine hydrochloride是一种有效的sigma-2受体激动剂。Siramesine对sigma-2受体具有亚纳摩尔亲和力 (IC 50 =0.12nM),并且对sigma-2受体的选择性是sigma-1受体的140倍(IC 50 =17nM)。
- GC15231Oleoyl Ethyl AmideCAS: 85075-82-7纯度: >98.00%
An endocannabinoid analog that inhibits FAAH and has analgesic activity
- GC15356Prion Protein 106-126 (human)CAS: 148439-49-0
PrP(106-126)是与朊病毒蛋白的淀粉样区域相对应的多肽段,它的生化特性类似于朊病毒蛋白的感染区域。
- GC15442Tipifarnib (Zarnestra)CAS: 192185-72-1纯度: >98.50%
A farnesyltransferase inhibitor with antitumor activity
- GC15530DapagliflozinCAS: 461432-26-8纯度: >99.50% / >98.00%
Dapagliflozin 是一种钠-葡萄糖协同转运蛋白 2 (SGLT2) 抑制剂,是一种新型抗糖尿病药物,由于其抑制 SGLT2 介导的肾葡萄糖重吸收的能力而被批准用于治疗 T2DM。
- GC15577Bestatin hydrochlorideCAS: 65391-42-6纯度: >99.50% / >99.00%
Bestatin hydrochloride是氨基肽酶N(APN/CD13)抑制剂,其IC 50 值为14.9±3.4μM。
- GC15681Liproxstatin-1CAS: 950455-15-9纯度: >98.00%
Liproxstatin-1 是一种有效的铁死亡抑制剂,可以防止铁死亡诱导剂,例如丁硫氨酸亚砜胺 (BSO)、erastin 和 (1S,3R)-RSL3 (RSL3)。
- GC15736Rosuvastatin CalciumCAS: 147098-20-2纯度: >99.50%
Rosuvastatin Calcium是一种竞争性HMG-CoA还原酶抑制剂,IC 50 值为11nM。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC15158 | Tioxolone | 4991-65-5 | >98.50% | |
A carbonic anhydrase I inhibitor | ||||
| GC15209 | WWL123 | 1338575-41-9 | - | |
A selective inhibitor of ABHD6 | ||||
| GC15210 | PF-622 | 898235-65-9 | - | |
A selective, potent FAAH inhibitor | ||||
| GC15222 | Siramesine hydrochloride | 224177-60-0 | >99.50% | |
Siramesine hydrochloride是一种有效的sigma-2受体激动剂。Siramesine对sigma-2受体具有亚纳摩尔亲和力 (IC 50 =0.12nM),并且对sigma-2受体的选择性是sigma-1受体的140倍(IC 50 =17nM)。 | ||||
| GC15231 | Oleoyl Ethyl Amide | 85075-82-7 | >98.00% | |
An endocannabinoid analog that inhibits FAAH and has analgesic activity | ||||
| GC15242 | Vardenafil | 224785-90-4 | - | |
Vardenafil 是一种具有口服活性的选择性磷酸二酯酶 5 (PDE5) 抑制剂,IC50 为 0.7 nM。 | ||||
| GC15244 | Thienyldecyl Isothiocyanate | 288323-41-1 | - | |
An antiproliferative isothiocyanate | ||||
| GC15257 | Perhexiline (maleate) | 6724-53-4 | >98.00% | |
Inhibitor of carnitine palmitoyltransferases | ||||
| GC15266 | Qc 1 | 403718-45-6 | >98.00% | |
Qc 1 是一种可逆的非竞争性苏氨酸脱氢酶 (TDH) 抑制剂。 | ||||
| GC15286 | Dimethyl DL-Glutamate (hydrochloride) | 13515-99-6 | - | |
A cell-permeant glutamate derivative | ||||
| GC15344 | SP 600125 | 129-56-6 | >98.00% | |
SP 600125是一种具有口服活性的、可逆的、具有选择性的ATP竞争性JNK 抑制剂,对JNK1、JNK2和JNK3的IC 50 分别为40、40和90nM。SP 600125常用于卵巢癌、肿瘤、帕金森病 (PD)、乳腺癌和哮喘的研究。 | ||||
| GC15356 | Prion Protein 106-126 (human) | 148439-49-0 | - | |
PrP(106-126)是与朊病毒蛋白的淀粉样区域相对应的多肽段,它的生化特性类似于朊病毒蛋白的感染区域。 | ||||
| GC15387 | TPPU | 1222780-33-7 | >99.00% / >98.00% | |
TPPU是一种可溶性环氧化物水解酶(sEH)抑制剂,对猴和人sEH的IC50值分别为37和3.7 nM。 | ||||
| GC15399 | Dp44mT | 152095-12-0 | >98.00% | |
An iron chelator with antiproliferative effects | ||||
| GC15442 | Tipifarnib (Zarnestra) | 192185-72-1 | >98.50% | |
A farnesyltransferase inhibitor with antitumor activity | ||||
| GC15445 | TMS | 24144-92-1 | >99.00% / >98.00% | |
TMS(2,3',4,5'-tetramethoxystilbene)是一种特异性强效的CYP1B1抑制剂,IC 50 值为6±2nmol/L。 | ||||
| GC15530 | Dapagliflozin | 461432-26-8 | >99.50% / >98.00% | |
Dapagliflozin 是一种钠-葡萄糖协同转运蛋白 2 (SGLT2) 抑制剂,是一种新型抗糖尿病药物,由于其抑制 SGLT2 介导的肾葡萄糖重吸收的能力而被批准用于治疗 T2DM。 | ||||
| GC15547 | Inosine-5'-monophosphate (sodium salt hydrate) | 20813-76-7 | - | |
A 5’-ribonucleoside | ||||
| GC15577 | Bestatin hydrochloride | 65391-42-6 | >99.50% / >99.00% | |
Bestatin hydrochloride是氨基肽酶N(APN/CD13)抑制剂,其IC 50 值为14.9±3.4μM。 | ||||
| GC15601 | AG-120 | 1448347-49-6 | >99.50% / >98.00% | |
AG-120 (Ivosidenib)是一种突变型异柠檬酸脱氢酶1(mIDH1)抑制剂。 | ||||
| GC15673 | CP 775146 | 702680-17-9 | - | |
A PPARα agonist | ||||
| GC15681 | Liproxstatin-1 | 950455-15-9 | >98.00% | |
Liproxstatin-1 是一种有效的铁死亡抑制剂,可以防止铁死亡诱导剂,例如丁硫氨酸亚砜胺 (BSO)、erastin 和 (1S,3R)-RSL3 (RSL3)。 | ||||
| GC15736 | Rosuvastatin Calcium | 147098-20-2 | >99.50% | |
Rosuvastatin Calcium是一种竞争性HMG-CoA还原酶抑制剂,IC 50 值为11nM。 | ||||
| GC15738 | BVT 2733 | 376640-41-4 | >98.00% | |
An 11β-HSD1 inhibitor | ||||
