Metabolism
Metabolism(代谢)
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Metabolism 相关产品(3072)
- GC19831SCD1 inhibitor-4CAS: 1295541-87-5纯度: >98.50%
SCD1 inhibitor-4 是一种有效的、具有口服活性的硬脂酰辅酶A 去饱和酶-1 (SCD1) 抑制剂。
- GC19839Trypsin inhibitor(soybean) (≥4000 BAEE Units/mg)CAS: 9035-81-8纯度: {{1-8}BA-≥4000 BAEE Units/mg / {9}BA-4000 BAEE Units/mg / {10}BA-4120 BAEE Units/mg} / {11}BA-4230BAEE U/mg}
Trypsin inhibitor(soybean)是一种胰蛋白酶(trypsin)抑制剂,IC 50 为19 µM,也可以抑制胰凝乳蛋白酶,IC 50 为14.3µM。
- GC198524-Methylumbelliferyl-α-D-glucopyranosideCAS: 17833-43-1纯度: >99.00%
A fluorogenic substrate for α-glucosidase
- GC19926Methyl malonic acidCAS: 108-59-8纯度: >99.50%
A dicarboxylic acid and byproduct of propionate catabolism
- GC20007Ginsenoside CKCAS: 39262-14-1纯度: >98.00%
Ginsenoside CK,一种由主要人参皂苷化合物转化而来的次级人参皂苷,比其母体人参皂苷具有更高的生物利用度和溶解性,具有极其重要的意义。
- GC20027(±)5(6)-DiHET MaxSpec® StandardCAS: 213382-49-1纯度: >95.00%
5(6)-DiHET is a fully racemic version of the enantiomeric forms biosynthesized from 5(6)-EET by epoxide hydrolases.
- GC200955,7-Dihydroxy-4-methylcoumarinCAS: 2107-76-8
A synthetic coumarin with diverse biological activities
- GC20109Cefotiam hexetil hydrochlorideCAS: 95789-30-3
Cefotiam hexetil hydrochloride 是可口服的第三代头孢菌素,是 cefotiam 的前药,但无抗菌作用。Cefotiam 是一种抗生素。
- GC25001(R)-AvanafilCAS: 1638497-26-3
R-Avanafil is a strong competitive inhibitor of phosphodiesterase 5 (PDE5) with a demonstrated in vitro IC 50 of 5.2 nM.
- GC25039AG-120 (racemic)CAS: 1448346-63-1
AG-120 (racemic), the racemic mixture of AG-120, is an orally available inhibitor of isocitrate dehydrogenase type 1 (IDH1) with potential antineoplastic activity.
- GC25137Betrixaban maleateCAS: 936539-80-9
Betrixaban maleate is the maleate salt form of Betrixaban, which is a Factor Xa inhibitor that decreases prothrombinase activity and thrombin generation.
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC19822 | SYRINGETIN | 4423-37-4 | >99.00% | |
丁香素是一种类黄酮衍生物,与 BMP-2 产量增加有关。 | ||||
| GC19824 | (±)-Pinocembrin | 68745-38-0 | >98.00% | |
A flavonoid with diverse biological activities | ||||
| GC19831 | SCD1 inhibitor-4 | 1295541-87-5 | >98.50% | |
SCD1 inhibitor-4 是一种有效的、具有口服活性的硬脂酰辅酶A 去饱和酶-1 (SCD1) 抑制剂。 | ||||
| GC19839 | Trypsin inhibitor(soybean) (≥4000 BAEE Units/mg) | 9035-81-8 | {{1-8}BA-≥4000 BAEE Units/mg / {9}BA-4000 BAEE Units/mg / {10}BA-4120 BAEE Units/mg} / {11}BA-4230BAEE U/mg} | |
Trypsin inhibitor(soybean)是一种胰蛋白酶(trypsin)抑制剂,IC 50 为19 µM,也可以抑制胰凝乳蛋白酶,IC 50 为14.3µM。 | ||||
| GC19852 | 4-Methylumbelliferyl-α-D-glucopyranoside | 17833-43-1 | >99.00% | |
A fluorogenic substrate for α-glucosidase | ||||
| GC19892 | Sodium chenodeoxycholate | 2646-38-0 | >98.00% | |
A primary bile acid | ||||
| GC19910 | 2,2',4,4'-Tetrabromodiphenyl Ether | 5436-43-1 | >95.00% | |
| GC19921 | Phenylarsine Oxide | 637-03-6 | >98.00% | |
An organoarsenic compound | ||||
| GC19926 | Methyl malonic acid | 108-59-8 | >99.50% | |
A dicarboxylic acid and byproduct of propionate catabolism | ||||
| GC19936 | Quisinostat dihydrochloride | 875320-31-3 | - | |
A pan-HDAC inhibitor | ||||
| GC19941 | DL-Leucic Acid | 498-36-2 | ≥98% | |
| GC20007 | Ginsenoside CK | 39262-14-1 | >98.00% | |
Ginsenoside CK,一种由主要人参皂苷化合物转化而来的次级人参皂苷,比其母体人参皂苷具有更高的生物利用度和溶解性,具有极其重要的意义。 | ||||
| GC20027 | (±)5(6)-DiHET MaxSpec® Standard | 213382-49-1 | >95.00% | |
5(6)-DiHET is a fully racemic version of the enantiomeric forms biosynthesized from 5(6)-EET by epoxide hydrolases. | ||||
| GC20062 | trans-3'-Hydroxycotinine | 34834-67-8 | >98.00% | |
A metabolite of nicotine | ||||
| GC20091 | α-Arbutin | 84380-01-8 | >99.00% | |
A glycosylated hydroquinone with diverse biological activities | ||||
| GC20095 | 5,7-Dihydroxy-4-methylcoumarin | 2107-76-8 | - | |
A synthetic coumarin with diverse biological activities | ||||
| GC20109 | Cefotiam hexetil hydrochloride | 95789-30-3 | - | |
Cefotiam hexetil hydrochloride 是可口服的第三代头孢菌素,是 cefotiam 的前药,但无抗菌作用。Cefotiam 是一种抗生素。 | ||||
| GC20142 | Beta-Sitosterol | 83-46-5 | >98.00% | |
Beta-Sitosterol是一种具有多种生物活性的植物甾醇,具有抗炎、抗肿瘤、退热和免疫调节等活性。 | ||||
| GC20169 | 5-Bromo-4-Chloro-3-Indolyl-Alpha-D-Galactopyranoside | 107021-38-5 | >98.00% | |
| GC25001 | (R)-Avanafil | 1638497-26-3 | - | |
R-Avanafil is a strong competitive inhibitor of phosphodiesterase 5 (PDE5) with a demonstrated in vitro IC 50 of 5.2 nM. | ||||
| GC25039 | AG-120 (racemic) | 1448346-63-1 | - | |
AG-120 (racemic), the racemic mixture of AG-120, is an orally available inhibitor of isocitrate dehydrogenase type 1 (IDH1) with potential antineoplastic activity. | ||||
| GC25097 | AQX-016A | 849669-54-1 | - | |
AQX-016A is a potent agonist of SHIP1. AQX-016A inhibits DNFB induced inflammation in a mouse ear edema/cutaneous anaphylaxis model. | ||||
| GC25137 | Betrixaban maleate | 936539-80-9 | - | |
Betrixaban maleate is the maleate salt form of Betrixaban, which is a Factor Xa inhibitor that decreases prothrombinase activity and thrombin generation. | ||||
| GC25331 | Dac51 | 2243944-92-3 (free base) | >99.00% | |
Dac51 is a potent FTO inhibitor with an IC50 of 0.4 μM for inhibiting FTO demethylation. | ||||
