Metabolism
Metabolism(代谢)
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Metabolism 相关产品(3072)
- GC31325Saroglitazar MagnesiumCAS: 1639792-20-3纯度: >98.50%
Saroglitazarmagnesium是一种新型的过氧化物酶体增殖物活化受体PPAR的激动剂,具有显著PPARα活性和中度PPARγ活性,在HepG2细胞中的EC50值分别为0.65pMand3nM。
- GC31350AstaxanthinCAS: 472-61-7纯度: >98.00%
Astaxanthin (β-Carotene-4,4'-dione, Trans-Astaxanthin), a xanthophyll carotenoid, is a nutrient with unique cell membrane actions and diverse clinical benefits with excellent safety and tolerability. Astaxanthin, a red dietary carotenoid isolated from Haematococcus pluvialis, is a modulator of PPARγ and a potent antioxidant with antiproliferative, neuroprotective and anti-inflammatory activity.
- GC31366Licogliflozin (LIK066)CAS: 1291094-73-9纯度: >98.00%
Licogliflozin (LIK066) 是一种钠葡萄糖协同转运蛋白(SGLT1 和 SGLT2)抑制剂。
- GC31377Tofogliflozin hydrate (CSG-452 hydrate)CAS: 1201913-82-7纯度: >98.50% / >98.00%
A potent inhibitor of SGLT2
- GC31396Raspberry ketone (Frambione)CAS: 5471-51-2纯度: >99.50%
Raspberry ketone (p-Hydroxybenzyl acetone, Frambinone, Oxyphenylon, Rheosmin, Rasketone) is a natural phenolic compound that is the primary aroma compound of red raspberries. Raspberry ketone shows cardioprotective action against isoproterenol-induced myocardial infarction in rats, and the effects may be due to its PPAR-α agonistic activity.
- GC31408Indeglitazar (PPM 204)CAS: 835619-41-5纯度: >99.50%
Indeglitazar (PPM 204) (PPM 204) 是一种可口服的 PPAR 泛激动剂,适用于所有三种 PPARα, PPARδ和PPARγ;。
- GC31422MCH-1 antagonist 1CAS: 1039825-68-7
MCH-1antagonist1是一种有效的黑色素浓缩激素1(MCH-1)拮抗剂,Ki值为2.6nM。MCH-1antagonist1还抑制CYP3A4,IC50为10μM。
- GC31450Naveglitazar racemateCAS: 916085-47-7
Naveglitazarracemate是Naveglitazar的外消旋体。Naveglitazar是过氧化物酶体增殖物激活受体(PPAR)α-γ双重,γ显性激动剂,在动物模型具有降低葡萄糖潜力。
- GC31451Peliglitazar racemate (BMS 426707-01 racemate)CAS: 331744-72-0
Peliglitazar 外消旋体(BMS 426707-01 外消旋体)是 Peliglitazar 的外消旋体。
- GC31461Tofogliflozin (CSG452)CAS: 903565-83-3
Tofogliflozin (CSG 452) is a novel sodium-glucose co-transporter 2(SGLT2) inhibitor with IC50 values of 2.9 nM and 8444 nM for hSGLT2 and hSGLT1, respectively.
- GC31479BMS-819881CAS: 1197420-05-5
BMS-819881是一种黑色素浓缩激素受体1(MCHR1)拮抗剂,结合大鼠MCHR1,Ki值为7nM。BMS-819881还有效且选择性地作用于CYP3A4,EC50为13μM.
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC31299 | Sch59498 | 224157-99-7 | - | |
Sch59498是一种有效的phosphodiesterase1c(Pde1c)抑制剂。 | ||||
| GC31324 | PTP1B-IN-2 | 1919853-46-5 | >99.50% | |
A PTP1B inhibitor | ||||
| GC31325 | Saroglitazar Magnesium | 1639792-20-3 | >98.50% | |
Saroglitazarmagnesium是一种新型的过氧化物酶体增殖物活化受体PPAR的激动剂,具有显著PPARα活性和中度PPARγ活性,在HepG2细胞中的EC50值分别为0.65pMand3nM。 | ||||
| GC31327 | Win 58237 | 158001-76-4 | - | |
Win58237是一种phosphodiesterase(PDE)抑制剂,对PDEV有很强的亲和力,Ki值为170nM,具有舒张血管的作用。 | ||||
| GC31345 | Retinol (Vitamin A1) | 68-26-8 | >98.00% | |
视黄醇,也称为维生素A 1 ,是维生素A家族中的一种脂溶性维生素,存在于食物中,用作膳食补充剂。 | ||||
| GC31350 | Astaxanthin | 472-61-7 | >98.00% | |
Astaxanthin (β-Carotene-4,4'-dione, Trans-Astaxanthin), a xanthophyll carotenoid, is a nutrient with unique cell membrane actions and diverse clinical benefits with excellent safety and tolerability. Astaxanthin, a red dietary carotenoid isolated from Haematococcus pluvialis, is a modulator of PPARγ and a potent antioxidant with antiproliferative, neuroprotective and anti-inflammatory activity. | ||||
| GC31355 | AA26-9 | 1312782-34-5 | >98.00% | |
A pan-serine hydrolase inhibitor | ||||
| GC31366 | Licogliflozin (LIK066) | 1291094-73-9 | >98.00% | |
Licogliflozin (LIK066) 是一种钠葡萄糖协同转运蛋白(SGLT1 和 SGLT2)抑制剂。 | ||||
| GC31377 | Tofogliflozin hydrate (CSG-452 hydrate) | 1201913-82-7 | >98.50% / >98.00% | |
A potent inhibitor of SGLT2 | ||||
| GC31396 | Raspberry ketone (Frambione) | 5471-51-2 | >99.50% | |
Raspberry ketone (p-Hydroxybenzyl acetone, Frambinone, Oxyphenylon, Rheosmin, Rasketone) is a natural phenolic compound that is the primary aroma compound of red raspberries. Raspberry ketone shows cardioprotective action against isoproterenol-induced myocardial infarction in rats, and the effects may be due to its PPAR-α agonistic activity. | ||||
| GC31408 | Indeglitazar (PPM 204) | 835619-41-5 | >99.50% | |
Indeglitazar (PPM 204) (PPM 204) 是一种可口服的 PPAR 泛激动剂,适用于所有三种 PPARα, PPARδ和PPARγ;。 | ||||
| GC31422 | MCH-1 antagonist 1 | 1039825-68-7 | - | |
MCH-1antagonist1是一种有效的黑色素浓缩激素1(MCH-1)拮抗剂,Ki值为2.6nM。MCH-1antagonist1还抑制CYP3A4,IC50为10μM。 | ||||
| GC31447 | CVT-12012 | 1018675-35-8 | >98.50% | |
A stearoyl-CoA desaturase inhibitor | ||||
| GC31450 | Naveglitazar racemate | 916085-47-7 | - | |
Naveglitazarracemate是Naveglitazar的外消旋体。Naveglitazar是过氧化物酶体增殖物激活受体(PPAR)α-γ双重,γ显性激动剂,在动物模型具有降低葡萄糖潜力。 | ||||
| GC31451 | Peliglitazar racemate (BMS 426707-01 racemate) | 331744-72-0 | - | |
Peliglitazar 外消旋体(BMS 426707-01 外消旋体)是 Peliglitazar 的外消旋体。 | ||||
| GC31452 | AVE-8134 | 304025-09-0 | - | |
AVE-8134是PPARα的有效激动剂,对人体和啮齿类动物的PPARα的EC50值分别为100和3000nM。 | ||||
| GC31460 | CDD3506 | 197913-15-8 | >98.00% | |
CDD3506可以通过诱导肝CYP3A的活动,来提高高密度脂蛋白胆固醇(HDL)的水平。 | ||||
| GC31461 | Tofogliflozin (CSG452) | 903565-83-3 | - | |
Tofogliflozin (CSG 452) is a novel sodium-glucose co-transporter 2(SGLT2) inhibitor with IC50 values of 2.9 nM and 8444 nM for hSGLT2 and hSGLT1, respectively. | ||||
| GC31462 | Arhalofenate (MBX 102) | 24136-23-0 | - | |
A prodrug form of a PPARγ partial agonist | ||||
| GC31464 | CDD3505 | 173865-33-3 | >98.00% | |
CDD3505 is used for elevating high density lipoprotein cholesterol (HDL) by inducing hepatic cytochrome P450IIIA (CYP3A) activity. | ||||
| GC31471 | GSK376501A | 1010412-80-2 | >99.00% | |
GSK376501A是一种选择性的过氧化物酶体增殖物激活受体γ(PPARγ)调节剂。可用于治疗2型糖尿病。 | ||||
| GC31479 | BMS-819881 | 1197420-05-5 | - | |
BMS-819881是一种黑色素浓缩激素受体1(MCHR1)拮抗剂,结合大鼠MCHR1,Ki值为7nM。BMS-819881还有效且选择性地作用于CYP3A4,EC50为13μM. | ||||
| GC31492 | Vildagliptin dihydrate (LAF237 dihydrate) | 2133364-01-7 | - | |
A DPP-4 inhibitor | ||||
| GC31497 | KD-3010 | 934760-92-6 | - | |
KD3010是一种具有口服活性的有效的选择性PPARδ激动剂。 | ||||
