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Metabolism 相关产品(3072)
- GC18106Calyculin ACAS: 101932-71-2纯度: >99.00% / >98.00% / >95.00%
Calyculin A是蛋白磷酸酶1（PP1）和蛋白磷酸酶2A（PP2A）的强效抑制剂, IC 50 值分别为2nM和0.5–1.0nM。
- GC18147Tretinoin (Aberela)CAS: 302-79-4纯度: >99.50% / >98.00%
Tretinoin (Aberela) 是一种维生素 A 衍生的非肽类亲脂性小分子，可作为核 RA 受体 (RAR) 的配体，将其从转录抑制因子转化为激活因子 .在培养的人系膜细胞中，维甲酸 (Aberela) 以剂量和时间依赖性方式增加还原型谷胱甘肽含量和过氧化氢酶活性，从而阻止 H2O2 的细胞毒性。
- GC1837215(S)-15-methyl Prostaglandin F2α methyl esterCAS: 35700-21-1
A methyl ester derivative of a potent uterine stimulant and abortifacient
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC18106 | Calyculin A | 101932-71-2 | >99.00% / >98.00% / >95.00% | |
Calyculin A是蛋白磷酸酶1（PP1）和蛋白磷酸酶2A（PP2A）的强效抑制剂, IC 50 值分别为2nM和0.5–1.0nM。 | ||||
| GC18141 | EA4 | 389614-94-2 | >98.50% | |
An inhibitor of PLA 2 from red blood cells | ||||
| GC18147 | Tretinoin (Aberela) | 302-79-4 | >99.50% / >98.00% | |
Tretinoin (Aberela) 是一种维生素 A 衍生的非肽类亲脂性小分子，可作为核 RA 受体 (RAR) 的配体，将其从转录抑制因子转化为激活因子 .在培养的人系膜细胞中，维甲酸 (Aberela) 以剂量和时间依赖性方式增加还原型谷胱甘肽含量和过氧化氢酶活性，从而阻止 H2O2 的细胞毒性。 | ||||
| GC18170 | ML-346 | 100872-83-1 | >98.00% | |
An activator of the heat shock response | ||||
| GC18174 | BIA 10-2474 | 1233855-46-3 | >98.00% | |
An inhibitor of FAAH | ||||
| GC18194 | 4-Epidoxycycline | 6543-77-7 | - | |
A metabolite of doxycycline | ||||
| GC18205 | 3,5-Diiodothyroacetic Acid | 1155-40-4 | >98.00% | |
A thyroid hormone derivative | ||||
| GC18209 | 4-Nitrophenyl β-D-Cellotetraoside | 129411-62-7 | - | |
A small molecule cellulose mimic | ||||
| GC18214 | AM2394 | 1442684-77-6 | >99.00% | |
A glucokinase activator | ||||
| GC18219 | 6-hydroxy Warfarin | 17834-02-5 | >98.00% | |
A phase I metabolite of (+)-warfarin | ||||
| GC18230 | ethyl 2,5-Dihydroxybenzoate | 3943-91-7 | - | |
A dual modulator of bone cell differentiation | ||||
| GC18239 | TPI-1 | 79756-69-7 | >98.00% | |
TPI-1（酪氨酸磷酸酶抑制剂1）是一种SHP-1抑制剂（IC 50 = 40nM），可用于研究黑色素瘤。 | ||||
| GC18245 | Stachyose | 470-55-3 | >80.00% | |
Stachyose是一种寡糖，也是一种益生元。 | ||||
| GC18252 | Diallyl Sulfide | 592-88-1 | >98.00% | |
An organosulfur compound | ||||
| GC18258 | CpdA | 14593-25-0 | >98.50% | |
A non-steroidal selective glucocorticoid receptor modulator | ||||
| GC18270 | 22(S)-hydroxy Cholesterol | 22348-64-7 | >95.00% | |
A synthetic oxysterol and LXR modulator | ||||
| GC18271 | Polmacoxib | 301692-76-2 | - | |
An inhibitor of COX-2 and carbonic anhydrase | ||||
| GC18284 | 7-Methyluric Acid | 612-37-3 | - | |
A methylated purine | ||||
| GC18286 | (R)-Mephenytoin | 71140-51-7 | >98.00% | |
An enantiomer of mephenytoin | ||||
| GC18305 | CAY10650 | 1233706-88-1 | >98.00% | |
CAY10650是一种高效的细胞质磷脂酶A2α（cPLA2α）抑制剂，IC 50 值为12nM。 | ||||
| GC18313 | BAR501 Impurity | 1632118-70-7 | - | |
A GP-BAR1 agonist | ||||
| GC18333 | Equilenin | 517-09-9 | - | |
An equine estrogen | ||||
| GC18335 | 6β-hydroxy Dexamethasone | 55879-47-5 | - | |
A metabolite of dexamethasone | ||||
| GC18372 | 15(S)-15-methyl Prostaglandin F2α methyl ester | 35700-21-1 | - | |
A methyl ester derivative of a potent uterine stimulant and abortifacient | ||||