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IDO

Indoleamine-pyrrole 2,3-dioxygenase (IDO) is a heme-containing enzyme physiologically expressed in several tissues and cells, such as the small intestine, lungs, female genital tract or placenta.IDO is involved in tryptophan metabolism. It is one of three enzymes that catalyze the first and rate-limiting step in the kynurenine pathway. IDO is an important part of the immune system and plays a part in natural defense against various pathogens. It is produced by the cells in response to inflammation and has an immunosuppressive function because of its ability to limit T-cell function and engage mechanisms of immune tolerance. IDO is part of the malignant transformation process and plays a key role in suppressing the anti-tumor immune response in the body, so inhibiting it could increase the effect of chemotherapy as well as other immunotherapeutic protocols.

Epacadostat
T35481204669-58-8
Epacadostat (INCB 024360) 是一种口服、高效且具有选择性的 IDO1 抑制剂,IC50值为71.8 nM。
  • ¥ 256
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TargetMol | Inhibitor Hot
TargetMol | Citations 客户已引用
Linrodostat
T45321923833-60-6
Linrodostat (BMS-986205) 是选择性的、不可逆的吲哚胺 2,3-双加氧酶 1(IDO1) 抑制剂,能够有效抑制 IDO1-HEK293 细胞,其IC50=1.1 nM。它在晚期癌症中具有良好的药理特性。
  • ¥ 319
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TargetMol | Inhibitor Hot
β-Lapachone
T64074707-32-8
β-Lapachone (ARQ-501) 是一种萘醌类天然产物,是拓扑异构酶 I 抑制剂,通过抑制细胞周期进程来诱导细胞凋亡。
  • ¥ 148
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TargetMol | Inhibitor Sale
TargetMol | Citations 客户已引用
PF-06840003
T4307198474-05-4
PF-06840003 (EOS200271) 是口服具有活力的、选择性的IDO-1抑制剂,抑制 hIDO-1, dIDO-1和 mIDO-1 的IC50分别为 0.41 μM, 0.59 μM,和 1.5 μM。
  • ¥ 243
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TargetMol | Inhibitor Sale
TargetMol | Citations 客户已引用
IDO-IN-12
T116151888341-29-4In house
IDO-IN-12 是吲哚胺 2,3-双加氧酶抑制剂。
  • ¥ 828
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TargetMol | Inhibitor Sale
LY3381916
T119012166616-75-5
LY3381916 是可透过血脑屏障的、选择性的IDO1抑制剂,能够与缺乏血红素的 apo-IDO1 结合,但无法与成熟血红素的 IDO1 结合。
  • ¥ 315
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IDO1-IN-1
T20513615-21-4
IDO1-IN-1 (2 HzBTZ) 是一种吲哚胺 2,3-双加氧酶 1 (IDO1) 抑制剂。
  • ¥ 99
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IDO5L
T2647914471-09-3
IDO5L (INCB024360 analogue) 是一种有效的吲哚胺-2,3-双加氧酶 (IDO) 抑制剂,IC50=67 nM。
  • ¥ 226
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GNF-PF-3777
T1019977603-42-0
GNF-PF-3777 (8-Nitrotryptanthrin) 是人吲哚胺2,3-双加氧酶 2 (hIDO2) 抑制剂,能够降低IDO2活性,Ki=为 0.97 μM。
  • ¥ 436
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TargetMol | Inhibitor Sale
BMS-986242
T91641923844-48-7
BMS-986242 是具有口服具有活力、强效的、选择性的 indoleamine-2,3-dioxygenase 1 抑制剂,可用于研究癌症。
  • ¥ 696
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TargetMol | Inhibitor Sale
IDO-IN-13
T116162291164-02-6
IDO-IN-13 (GS-4361) 是 indoleamine 2,3-dioxygenase 1 抑制剂,EC50=17 nM。
  • ¥ 516
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TargetMol | Inhibitor Sale
Kushenol E
T821499119-72-9
Kushenol E (Flemiphilippinin D) 是一种分离自Sophora flavescens 中的类黄酮,是一种IDO1的非竞争性抑制剂,其IC50=7.7 µM,Ki=为 9.5 µM,具有抗肿瘤特性。
  • ¥ 2900
5日内发货
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IACS-8968 R-enantiomer
T116272239305-67-8
IACS-8968 R-enantiomer is the R-enantiomer of IACS-8968. IACS-8968 is a dual IDO and TDO inhibitor (pIC50s: 6.43 for IDO and <5 for TDO).
  • ¥ 10600
6-8周
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IDO-IN-11
T116141888378-32-2
IDO-IN-11 is an indoleamine-2,3-dioxygenase (IDO) inhibitor with IC50s of 0.18 μM (Kinase) and 0.014 μM (Hela Cell).
  • ¥ 14800
6-8周
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IDO-IN-6
T116201402837-76-6
IDO-IN-6 is an indoleamine 2,3-dioxygenase (IDO) inhibitor.
  • ¥ 9990
6-8周
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IDO-IN-9
T116221888378-12-8
IDO-IN-9 is an indoleamine-2,3-dioxygenase (IDO) inhibitor with IC50s of 0.011 μM (Kinase) and 0.0018 μM (Hela Cell).
  • ¥ 12800
8-10周
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IDO1-IN-2
T116242346614-58-0
IDO1-IN-2 is a potent and selective IDO1 inhibitor with IC50s of 81 nM, 59 nM (mouse), and 28 nM (rat), respectively. It has anti-cancer activity.
  • ¥ 10600
6-8周
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IACS-8968 S-enantiomer
T116282239305-70-3
IACS-8968 S-enantiomer is the S-enantiomer of IACS-8968. IACS-8968 is a dual IDO and TDO inhibitor (pIC50s: 6.43 for IDO and <5 for TDO).
  • ¥ 10600
6-8周
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IDO-IN-3
T116172070018-30-1
IDO-IN-3 is a potent indoleamine 2,3-dioxygenase (IDO) inhibitor (IC50: 290 nM).
  • ¥ 1890
6-8周
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IDO-IN-8
T116211402837-77-7
IDO-IN-8 is an indoleamine 2,3-dioxygenase (IDO) inhibitor (IC50: 1-10 μM).
  • ¥ 9990
6-8周
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IACS-8968
T116262144425-14-7
IACS-8968 is a dual IDO and TDO inhibitor (pIC50s: 6.43 for IDO and <5 for TDO).
  • ¥ 11700
6-8周
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IDO-IN-5
T116191402837-79-9
IDO-IN-5 is an indoleamine 2,3-dioxygenase (IDO) inhibitor (IC50: 1-10 μM).
  • ¥ 9990
6-8周
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