IDO
IDO(吲哚胺2,3-双加氧酶)
Indoleamine 2,3-dioxygenase (IDO) is an enzyme catalyzing the oxidative degradation of L-tryptophan in the kynurenine pathway, in which the pyrrole ring of L-tryptophan is cleaved to generate N-formyl-kynurenine. Mature human IDO enzyme is a 45 kDa monomeric protein of 403 amino acids that is encoded by the IDO gene (15 kb with 10 exons). According to X-ray crystallographic analysis, the chemical structure of human IDO enzyme consists of two distinct α-helical domains (one small and one large) and a heme prosthetic group, where the heme is coordinated to the active site by a histidine (His) imidazole as the proximal fifth ligand.
IDO 相关产品(45)
- GC11008Necrostatin-1CAS: 4311-88-0纯度: >98.00% / >99.00%
Necrostatin-1主要作用于细胞中的RIP1,Necrostatin-1是一种RIP1激酶抑制剂,IC50值为0.32 mM。
- GC17968INCB-024360CAS: 1204669-58-8纯度: >99.50%
INCB-024360,又名epacadostat,是一种口服小分子选择性IDO1抑制剂(IC 50 = 71.8nM)。
- GC19079BMS-986205CAS: 1923833-60-6纯度: >99.50%
BMS-986205是一种选择性的不可逆的吲哚胺2,3-双加氧酶1(IDO1)的抑制剂,在过表达人IDO1的HEK293细胞中,IC 50 值为1.1μM。
- GC33671GNF-PF-3777 (8-Nitrotryptanthrin)CAS: 77603-42-0
A tryptanthrin derivative with diverse biological activities
- GC34137IDO-IN-5 (NLG-1489)CAS: 1402837-79-9
IDO-IN-5 (NLG-1489) (NLG-1489) 是一种吲哚胺 2,3-双加氧酶 (IDO) 抑制剂,提取自专利 WO WO2012142237A1,化合物 1489,IC50 为 1-10 μM.
- GC34139IDO-IN-8 (NLG-1487)CAS: 1402837-77-7纯度: >99.50%
IDO-IN-8 (NLG-1487) (NLG-1487) 是一种吲哚胺 2,3-双加氧酶 (IDO) 抑制剂,提取自专利 WO WO2012142237A1,化合物 1487,IC50 为 1-10 μM.
- GC34149IDO-IN-6 (NLG-1486)CAS: 1402837-76-6纯度: >99.50%
IDO-IN-6 (NLG-1486) (NLG-1486) 是一种吲哚胺 2,3-双加氧酶 (IDO) 抑制剂,提取自专利 WO WO2012142237A1,化合物 1486,IC50 <1 μM.
- GC34622IACS-8968 R-enantiomerCAS: 2239305-67-8纯度: >98.00%
IACS-8968(R-enantiomer)是IACS-8968的R型对映异构体。IACS-8968是IDO和TDO的双抑制剂,其pIC50s值分别为6.43,<5。
- GC34623IACS-8968 S-enantiomerCAS: 2239305-70-3纯度: >98.00%
IACS-8968(S-enantiomer)是IACS-8968的S型对映异构体。IACS-8968是IDO和TDO的双抑制剂,其pIC50s值分别为6.43,<5。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC13912 | NLG919 | 1402836-58-1 | >99.50% | |
An IDO pathway inhibitor | ||||
| GC14425 | IDO inhibitor 1 | 1204669-37-3 | - | |
Indoleamine-2,3-dioxygenase inhibitor | ||||
| GC11008 | Necrostatin-1 | 4311-88-0 | >98.00% / >99.00% | |
Necrostatin-1主要作用于细胞中的RIP1,Necrostatin-1是一种RIP1激酶抑制剂,IC50值为0.32 mM。 | ||||
| GC11066 | Indoximod (NLG-8189) | 110117-83-4 | >99.00% | |
An inhibitor of indoleamine 2,3-dioxygenase | ||||
| GC13519 | Navoximod | 1402837-78-8 | >99.00% | |
Navoximod (GDC-0919; NLG-919) 是一种有效的 IDO(吲哚胺-(2,3)-双加氧酶)通路抑制剂,Ki/EC50 为 7 nM/75 nM。 | ||||
| GC15833 | Norharmane | 244-63-3 | >98.00% | |
A co-mutagenic heterocyclic amine | ||||
| GC15846 | INCB024360 analogue | 914471-09-3 | >98.00% | |
A selective IDO1 inhibitor | ||||
| GC15876 | IDO-IN-1 | 914638-30-5 | >98.00% | |
A potent IDO inhibitor | ||||
| GC17968 | INCB-024360 | 1204669-58-8 | >99.50% | |
INCB-024360,又名epacadostat,是一种口服小分子选择性IDO1抑制剂(IC 50 = 71.8nM)。 | ||||
| GC19079 | BMS-986205 | 1923833-60-6 | >99.50% | |
BMS-986205是一种选择性的不可逆的吲哚胺2,3-双加氧酶1(IDO1)的抑制剂,在过表达人IDO1的HEK293细胞中,IC 50 值为1.1μM。 | ||||
| GC32879 | PF-06840003 (EOS200271) | 198474-05-4 | >98.00% | |
An inhibitor of IDO-1 | ||||
| GC32899 | IDO-IN-4 | 1629125-65-0 | >99.00% | |
IDO-IN-4 (IDO-IN-4) 是一种吲哚胺 2,3-双加氧酶 1 (IDO-1) 抑制剂,提取自专利 WO2014150677A1,化合物实施例 1 对映异构体 1。 | ||||
| GC33012 | IDO-IN-2 | 1668565-74-9 | >99.50% | |
An IDO1 inhibitor | ||||
| GC33058 | IDO-IN-3 | 2070018-30-1 | >99.50% | |
An inhibitor of IDO1 | ||||
| GC33191 | IDO-IN-9 | 1888378-12-8 | - | |
IDO-IN-9是一个吲哚胺-2,3-双加氧酶(IDO)抑制剂,在激酶实验和Hela细胞实验中的IC50值分别为0.011和0.0018μM,来自专利WO2016041489A1,化合物6。 | ||||
| GC33287 | LY-3381916 | 2166616-75-5 | >98.00% | |
An IDO1 inhibitor | ||||
| GC33671 | GNF-PF-3777 (8-Nitrotryptanthrin) | 77603-42-0 | - | |
A tryptanthrin derivative with diverse biological activities | ||||
| GC33963 | IDO-IN-12 | 1888341-29-4 | >98.00% | |
IDO-IN-12是一个吲哚胺2,3-双加氧酶(IDO)抑制剂,来自专利WO2017181849A1。 | ||||
| GC34137 | IDO-IN-5 (NLG-1489) | 1402837-79-9 | - | |
IDO-IN-5 (NLG-1489) (NLG-1489) 是一种吲哚胺 2,3-双加氧酶 (IDO) 抑制剂,提取自专利 WO WO2012142237A1,化合物 1489,IC50 为 1-10 μM. | ||||
| GC34139 | IDO-IN-8 (NLG-1487) | 1402837-77-7 | >99.50% | |
IDO-IN-8 (NLG-1487) (NLG-1487) 是一种吲哚胺 2,3-双加氧酶 (IDO) 抑制剂,提取自专利 WO WO2012142237A1,化合物 1487,IC50 为 1-10 μM. | ||||
| GC34149 | IDO-IN-6 (NLG-1486) | 1402837-76-6 | >99.50% | |
IDO-IN-6 (NLG-1486) (NLG-1486) 是一种吲哚胺 2,3-双加氧酶 (IDO) 抑制剂,提取自专利 WO WO2012142237A1,化合物 1486,IC50 <1 μM. | ||||
| GC34621 | IACS-8968 | 2144425-14-7 | >98.00% | |
IACS-8968是IDO和TDO的双抑制剂,其pIC50s值分别为6.43,<5。 | ||||
| GC34622 | IACS-8968 R-enantiomer | 2239305-67-8 | >98.00% | |
IACS-8968(R-enantiomer)是IACS-8968的R型对映异构体。IACS-8968是IDO和TDO的双抑制剂,其pIC50s值分别为6.43,<5。 | ||||
| GC34623 | IACS-8968 S-enantiomer | 2239305-70-3 | >98.00% | |
IACS-8968(S-enantiomer)是IACS-8968的S型对映异构体。IACS-8968是IDO和TDO的双抑制剂,其pIC50s值分别为6.43,<5。 | ||||
