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Cat. No. | Product Name | Target | Signaling Pathways |
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T3011L |
Kynurenine sulfate monohydrate
L-Kynurenine sulfate monohydrate |
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Kynurenine sulfate monohydrate is a precursor of kynurenic acid which is the only recognized endogenous excitatory amino acid receptor antagonist agent in the central nervous system. L-Kyn is known to be a pigment generating component in animals. In mamma | |||
T37683 |
3-Hydroxykynurenine
3-hydroxy-DL-Kynurenine,DL-3-Hydroxykynurenine |
Others | Others |
3-Hydroxykynurenine (3-hydroxy-DL-Kynurenine) 是色氨酸的活性代谢物,可抑制酵母和大鼠肝脏醛脱氢酶 97% 和 69%。 | |||
T72430 |
L-Kynurenine sulfate
|
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L-Kynurenine sulfate 是一种芳香烃受体AHR 激动剂,可激活 AHR 导向的初始T 细胞极化至抗炎 Treg 表型。 | |||
T1896 |
Ro 61-8048
|
Hydroxylase | Metabolism |
Ro 61-8048 是一种选择性的、口服有效的犬尿氨酸 3-羟化酶抑制剂(IC50:37 nM)。它能够导致细胞喹啉酸浓度的显著增加。 | |||
T4410 |
LM10
|
Others | Others |
LM10 是有效的色氨酸 2,3-双加氧酶的抑制剂。色氨酸 2,3-双加氧酶是一种无关的肝酶,它可通过犬尿氨酸途径降解色氨酸。它对研究癌症疾病具有潜在的研究价值。 | |||
T71760 |
4-Chlorokynurenine
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4-Chlorokynurenine is a prodrug of 7-Cl-kynurenic acid (7-Cl-KYNA), a potent, selective antagonist of the NMDA/glycine receptor. | |||
T28368 |
PF-04859989 HCl
PF 04859989,PF04859989,PF-04859989HCl,PF-04859989 |
Others | Others |
PF-04859989 HCl 是不可逆的犬尿氨酸转氨酶 KAT II 抑制剂,可透过血脑屏障,抑制 hKATⅡ 和 rKATⅡ 的 IC50分别为 23 和 263 nM。它对 KATⅡ 的选择性高于人 KATⅠ、KATⅢ 和 KATⅣ (IC50分别为22、11和 >50 μM)。 | |||
T26785 |
BFF122
BFF 122,BF5,BFF-122 |
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BFF122 is an inhibitor of kynurenine aminotransferase II (KAT II). | |||
T70041 |
GSK065
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GSK065 is a potent inhibitor of kynurenine-3-monooxygenase (KMO). | |||
T15426 | GSK180 | Hydroxylase | Metabolism |
GSK180 is a selective competitive inhibitor of kynurenine 3-monooxygenase (KMO; IC50: ~6 nM), an enzyme involved in tryptophan metabolism. | |||
T70701 |
CHDI340246
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CHDI-340246 is a potent and selective kynurenine mono-oxygenase (KMO) inhibitor. | |||
T11470 |
GSK 366
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Hydroxylase | Metabolism |
GSK 366 is a potent kynurenine-3-monooxygenase (KMO) inhibitor (IC50s: 0.7 nM and 2.3 nM for P. fluorescens-KMO and human KMO). | |||
T13258L | UPF-648 | Others | Others |
UPF-648 is a potent kynurenine 3-monooxygenase inhibitor. It also shows highly active at 1 uM (81 ± 10% KMO inhibition). | |||
T13258 | UPF-648 sodium salt | Others | Others |
UPF-648 sodium salt is an inhibitor of kynurenine 3-monooxygenase (KMO) and exhibits highly active at 1 uM (81 ± 10% KMO inhibition). | |||
T63613 |
JM6
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JM6 是弱犬尿氨酸 3-单加氧酶 (kynurenine 3-monooxygenase, KMO) 抑制剂,能够作用于小鼠 KMO (IC50: 19.85 μM)。JM6 能够用于研究阿尔茨海默病。 | |||
T4532L |
Linrodostat mesylate
ONO-7701,BMS-986205,ONO 7701,BMS986205,BMS 986205 |
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Linrodostat (BMS-986205, ONO-7701, and F001287) is a selective and orally active IDO1 inhibitor with potential immunomodulating and antineoplastic activities. By inhibiting IDO1 and reducing kynurenine in tumor cells, BMS-986205 restores and promotes the | |||
T69944 |
NLG802 HCl
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NLG802 is an orally bioavailable prodrug of indoximod, a methylated tryptophan, with immune checkpoint inhibitory and antineoplastic activities. Upon oral administration, the indoximod prodrug NLG802 is converted to indoximod. Indoximod targets, binds to and inhibits the enzyme indoleamine 2,3-dioxygenase (IDO; IDO1), which converts the essential amino acid tryptophan into the immunosuppressive metabolite kynurenine. By increasing tryptophan levels and decreasing kynurenine levels, indoximod res... | |||
T24617 |
PF-04859989
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PF-04859989 is a brain-penetrable irreversible inhibitor of kynurenine amino transferase II. PF-04859989 is ~1000-fold selective for KAT II over human KAT I, KAT III, and KAT IV. PF-04859989 has IC50 values of 23 nM for hKAT II and 263 nM for rKAT II. | |||
T73581 | HI5 | ||
HI5 是一种有效的微管蛋白 (tublin)和IDO 抑制剂,对 HeLa 细胞的IC50为 70 nM。HI5 抑制IDO 的表达,减少犬尿氨酸的产生,从而刺激 T 细胞活化和增殖。HI5 对 HeLa 细胞可抑制微管蛋白聚合和细胞迁移,引起 G2/M 期阻滞,同时通过线粒体依赖性凋亡途径诱导细胞凋亡 (apoptosis) 并引起反应性氧化应激。HI5 可用于抗癌研究。 |
Cat. No. | Product Name | Target | Signaling Pathways |
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T4928 |
L-Kynurenine
L-犬尿氨酸,(S)-Kynurenine |
AhR; Aryl Hydrocarbon Receptor; Endogenous Metabolite | Immunology/Inflammation; Metabolism |
L-Kynurenine ((S)-Kynurenine) 是L-色氨酸的代谢物,是芳香烃受体激动剂,可抑制同种异体 T 细胞增殖并增加恶性 U87 神经胶质瘤细胞侵入胶原基质。 | |||
T10938 |
D-Kynurenine
D-尿嘧啶,(R)-2-Amino-4-(2-aminophenyl)-4-oxobutanoic acid,ZINC901103 |
GPR; AhR; Endogenous Metabolite | Endocrinology/Hormones; GPCR/G Protein; Immunology/Inflammation; Metabolism |
D-Kynurenine (ZINC901103) 是 D-色氨酸的代谢物和 GPR109B 的激动剂。 D-Kynurenine 激活 AhR 并促进上皮细胞向间充质的转化。 D-Kynurenine 在 D-氨基酸氧化酶的荧光分析中用作底物。 | |||
T3011 |
2-Amino-4-(2-aminophenyl)-4-oxobutanoic acid
Kynurenine,Dl-Kynurenine,Kynurenin,3-Anthraniloylalanine,犬尿氨酸 |
Others; Endogenous Metabolite | Metabolism; Others |
2-Amino-4-(2-aminophenyl)-4-oxobutanoic acid (3-Anthraniloylalanine) 是一种酮类和氨基酸衍生物,具有多种生物功能,包括血管舒张、免疫调节和神经调节活性。2-Amino-4-(2-aminophenyl)-4-oxobutanoic acid 是烟酸的前体。2-Amino-4-(2-aminophenyl)-4-oxobutanoic acid 的异常产生与神经系统疾病相关的认知缺陷和抑郁症状有关。2-Amino-4-(2-aminophenyl)-4-oxobutanoic acid 在某些类型的癌细胞中过度表达,可能被用作评估癌症风险的生物标志物。 | |||
T4096 |
Quinolinic acid
喹啉酸,pyridine-2,3-dicarboxylic acid,QUIN |
Endogenous Metabolite; NMDAR; iGluR | Membrane transporter/Ion channel; Metabolism; Neuroscience |
Quinolinic acid (QUIN) 是一种内源性 N-甲基-D-天冬氨酸 (NMDA) 受体激动剂,由 L-色氨酸通过犬尿氨酸途径合成,具有调节 NMDA 神经元损伤和功能障碍的潜力。 | |||
T4707 |
3-Hydroxyanthranilic acid
3-HYDROXY-2-AMINOBENZOIC ACID,3-羟基-2-氨基苯甲酸 |
Others; Endogenous Metabolite | Metabolism; Others |
3-Hydroxyanthranilic acid (3-HYDROXY-2-AMINOBENZOIC ACID) 是犬尿氨酸途径中的色氨酸代谢物。它已在人类表皮和膀胱组织中发现,并且在多种生物体液中也已检测到,例如尿液和血液。在细胞内,它主要位于细胞质中。 它存在于从酵母到人类的所有真核生物中。 | |||
T80656 |
Cannflavin A
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Cannflavin A,源自大麻(Cannabis sativa L),具备抗癌、神经保护及抗炎活性。该化合物有效抑制Aβ1-42的聚集,并阻断犬尿氨酸-3-单加氧酶(KMO)的活性,进而通过caspase-3裂解途径激活细胞凋亡(apoptosis)。 |