Metabolism
Metabolism(代谢)
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Metabolism 相关产品(3072)
- GC30681RevexeprideCAS: 219984-49-3
Revexepride是一种高度选择性的5-HT4receptor激动剂,也是潜在的CYP3A4enzyme诱导剂,可用于治疗胃食管返流疾病。
- GC30705Veledimex S enantiomer (INXN-1001 S enantiome)CAS: 1093131-03-3纯度: >99.50%
Veledimex S 对映体 (INXN-1001 S enantiomer) 是 veledimex 的 S 对映体。 Veledimex 是专有基因治疗启动子系统的口服激活剂配体,也是 CYP3A4/5 的中度抑制剂和底物。
- GC30788L-Glutamic acid monosodium salt (Monosodium glutamate)CAS: 142-47-2纯度: >98.00% / >99.50%
L-Glutamic acid monosodium salt is the sodium salt of glutamic acid, found naturally in tomatoes, cheese and other foods. L-Glutamic acid monosodium salt acts as an excitatory transmitter and an agonist at all subtypes of glutamate receptors (metabotropic, kainate, NMDA, and AMPA). (S)-Glutamic acid shows a direct activating effect on the release of DA from dopaminergic terminals.
- GC30834Rilapladib (SB 659032)CAS: 412950-08-4纯度: >99.50%
Rilapladib (SB 659032) (SB 659032) 是一种选择性 Lp-PLA2(脂蛋白相关磷脂酶 A2)抑制剂,IC50 为 230 pM。
- GC30915BAY 73-6691 racemateCAS: 794568-90-4纯度: >99.50%
BAY73-6691racemate是一个磷酸二酯酶9(phosphodiesterase9)抑制剂,来自专利WO2017070293A1。
- GC30923BAY 73-6691 ((R)-BAY 73-6691)CAS: 794568-92-6纯度: >99.50%
BAY 73-6691 ((R)-BAY 73-6691) ((R)-BAY 73-6691 ((R)-BAY 73-6691)) 是一种有效的脑渗透选择性 PDE9A 抑制剂。
- GC31141Antihistamine-1CAS: 1186430-60-3
Antihistamine-1是能够渗透血脑屏障的H1-抗组胺药(Ki=6.9nM),它也是CYP2D6和hERG通道的抑制剂,其IC50值分别为5.4和0.8μM。
- GC31229AMPD2 inhibitor 1CAS: 2139356-35-5
AMPD2inhibitor1是一种腺苷单磷酸脱氨酶2(AMPD2)抑制剂,可用于研究对糖、盐和鲜味的渴望,以及对毒品、烟草、尼古丁和酒精上瘾的嗜好。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC30664 | Enocyanin | 11029-12-2 | - | |
Enocyanin是从葡萄中得到的花青素。Enocyanin可影响亮氨酸氨基肽酶、酸性磷酸酶(acidphosphatase)、γ-谷氨酰转肽酶和酯酶的活性。 | ||||
| GC30681 | Revexepride | 219984-49-3 | - | |
Revexepride是一种高度选择性的5-HT4receptor激动剂,也是潜在的CYP3A4enzyme诱导剂,可用于治疗胃食管返流疾病。 | ||||
| GC30705 | Veledimex S enantiomer (INXN-1001 S enantiome) | 1093131-03-3 | >99.50% | |
Veledimex S 对映体 (INXN-1001 S enantiomer) 是 veledimex 的 S 对映体。 Veledimex 是专有基因治疗启动子系统的口服激活剂配体,也是 CYP3A4/5 的中度抑制剂和底物。 | ||||
| GC30751 | FAAH-IN-1 | 1242441-47-9 | - | |
FAAH-IN-1是脂肪酸酰胺水解酶(FAAH)抑制剂,对大鼠和人FAAH的IC50值分别为145nM和650nM。 | ||||
| GC30754 | SHP2 IN-1 | 1801764-90-8 | - | |
SHP2IN-1(compound13)是SHP2(PTPN11)的变构抑制剂,其IC50值为3nM。 | ||||
| GC30788 | L-Glutamic acid monosodium salt (Monosodium glutamate) | 142-47-2 | >98.00% / >99.50% | |
L-Glutamic acid monosodium salt is the sodium salt of glutamic acid, found naturally in tomatoes, cheese and other foods. L-Glutamic acid monosodium salt acts as an excitatory transmitter and an agonist at all subtypes of glutamate receptors (metabotropic, kainate, NMDA, and AMPA). (S)-Glutamic acid shows a direct activating effect on the release of DA from dopaminergic terminals. | ||||
| GC30811 | ITI214 | 1642303-38-5 | >99.50% | |
A PDE1 inhibitor | ||||
| GC30828 | PF-05180999 | 1394033-54-5 | >98.50% | |
A PDE2A inhibitor | ||||
| GC30834 | Rilapladib (SB 659032) | 412950-08-4 | >99.50% | |
Rilapladib (SB 659032) (SB 659032) 是一种选择性 Lp-PLA2(脂蛋白相关磷脂酶 A2)抑制剂,IC50 为 230 pM。 | ||||
| GC30841 | ITI214 free base | 1160521-50-5 | >98.00% | |
A PDE1 inhibitor | ||||
| GC30879 | PDE1-IN-2 | 1904611-63-7 | >98.00% | |
PDE1-IN-2是PDE1的抑制剂,来自专利WO2016/55618A1,化合物实例31。对PDE1C,PDE1B和PDE1A的IC50值分别为6,140和164nM。 | ||||
| GC30899 | Sultiame | 61-56-3 | >99.50% | |
A pan-CA inhibitor and an anticonvulsant | ||||
| GC30915 | BAY 73-6691 racemate | 794568-90-4 | >99.50% | |
BAY73-6691racemate是一个磷酸二酯酶9(phosphodiesterase9)抑制剂,来自专利WO2017070293A1。 | ||||
| GC30923 | BAY 73-6691 ((R)-BAY 73-6691) | 794568-92-6 | >99.50% | |
BAY 73-6691 ((R)-BAY 73-6691) ((R)-BAY 73-6691 ((R)-BAY 73-6691)) 是一种有效的脑渗透选择性 PDE9A 抑制剂。 | ||||
| GC30966 | Olivetol | 500-66-3 | >99.50% | |
An Analytical Reference Standard | ||||
| GC30978 | PDE10-IN-1 | 1516896-09-5 | - | |
PDE10-IN-1是出自专利WO2013192273A1中的PDE10高效抑制剂。 | ||||
| GC30985 | Methysticin (DL-Methysticin) | 20697-20-5 | - | |
A natural kava lactone | ||||
| GC31103 | Arimoclomol maleate (BRX-220) | 289893-26-1 | >99.50% | |
A co-inducer of heat shock proteins | ||||
| GC31118 | KU-32 | 956498-70-7 | - | |
KU-32是一种新型的,基于新生霉素的Hsp90抑制剂,可以预防神经细胞死亡。 | ||||
| GC31141 | Antihistamine-1 | 1186430-60-3 | - | |
Antihistamine-1是能够渗透血脑屏障的H1-抗组胺药(Ki=6.9nM),它也是CYP2D6和hERG通道的抑制剂,其IC50值分别为5.4和0.8μM。 | ||||
| GC31213 | AMG 579 | 1227067-61-9 | >99.50% | |
AMG579是有效,选择性的磷酸二酯酶10A(PDE10A)抑制剂,IC50值为0.1nM。 | ||||
| GC31229 | AMPD2 inhibitor 1 | 2139356-35-5 | - | |
AMPD2inhibitor1是一种腺苷单磷酸脱氨酶2(AMPD2)抑制剂,可用于研究对糖、盐和鲜味的渴望,以及对毒品、烟草、尼古丁和酒精上瘾的嗜好。 | ||||
| GC31239 | SA72 | 934809-60-6 | - | |
SA72是高度选择性的脂肪酸酰胺水解酶(FAAH)抑制剂。 | ||||
| GC31258 | L791943 | 192767-01-4 | - | |
L791943是一种有效且有选择性的Phosphodiesterase-4(PDE4)抑制剂,其IC50值为4.2nM。 | ||||
