Cell Metabolism
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PX20606 trans-isomer
Catalog No. A16997 FXR 激动剂PX20606 trans-isomer在小鼠和猴子中诱导高密度脂蛋白介导的跨肝胆固醇外流,并预防胆固醇酯转移蛋白转基因低密度脂蛋白受体(-/-)mice的动脉粥样硬化。 了解更多 -
Mutant IDH1 inhibitor
Catalog No. A21150 mutant IDH1 R132H inhibitorMutant IDH1 inhibitor is a potent mutant IDH1 R132H inhibitor with IC50 of < 72 nM. 了解更多 -
Mutant IDH1-IN-2
Catalog No. A21339 IDH inhibitorMutant IDH1-IN-2 is a inhibitor of mutant Isocitrate dehydrogenase (IDH) proteins, with IC50 of in LS-MS biochemical assay, IC50 of 16.6 nM in Fluorescence biochemical assay. 了解更多 -
Mutant IDH1-IN-1
Catalog No. A21359 mutant-selective IDH1 inhibitorMutant IDH1-IN-1 is a mutant-selective IDH1 inhibitor with with IC50s of 4, 42, 80 and 143 nM against mutant IDH1 R132C/R132C, IDH1 R132H/R132H, IDH1 R132H/WT and wild type IDH1, respectively. 了解更多 -
AGI-5198 (IDH-C35)
Catalog No. A12902 -
Enasidenib
Catalog No. A15808 IDH2 抑制剂Enasidenib是一种有效的选择性IDH2抑制剂,具有潜在的抗癌活性(IDH2 =异柠檬酸脱氢酶2)。 了解更多 -
AG-120 (Ivosidenib)
Catalog No. A14386 -
Vorasidenib
Catalog No. A16908 IDH1 抑制剂Vorasidenib (AG-881)是一种有效且选择性的口服抑制剂,可抑制细胞质中异柠檬酸脱氢酶1型(IDH1,IDH1 [NADP+]可溶)和2型(IDH2异柠檬酸脱氢酶[NADP+])的突变形式。线粒体中的线粒体,具有潜在的抗肿瘤活性。 了解更多 -
BAY-1436032
Catalog No. A17059 -
Olutasidenib (FT-2102)
Catalog No. A18789 IDH1 inhibitorOlutasidenib is a potent, selective inhibitor of mutant Isocitrate dehydrogenase (IDH)1 for the treatment of acute myeloid leukemia. 了解更多 -
Mutant IDH1-IN-4
Catalog No. A19106 IDH1 inhibitorMutant IDH1-IN-4 (compound 434) is an inhibitor of mutant Isocitrate dehydrogenase 1 (IDH 1), with IC50 values of ?? 0.5 μM for mutant IDH1 in R132H, HT1080 and U87R132H cells. 了解更多 -
IDH1 Inhibitor 2
Catalog No. A18420 IDH1 inhibitorDH1 Inhibitor 2 is a potent IDH1 inhibitor via a direct covalent modification of His315, with an IC50 of 110 nM. 了解更多 -
Epacadostat (INCB024360)
Catalog No. A15554 IDO 抑制剂Epacadostat (INCB024360)是一种有效的选择性吲哚胺2,3-二加氧酶(IDO1)抑制剂,第2期的IC50为10 nM。 了解更多 -
IDO/TDO-IN-1
Catalog No. A18566 IDO/TDO dual inhibitorIDO/TDO-IN-1 is a highly potent and orally active dual indoleamine-2,3-dioxygenase (IDO) and tryptophan 2,3-dioxygenase (TDO) inhibitor with IC50s of 9.7 and 47 nM, respectively . 了解更多 -
GNF-PF-3777
Catalog No. A13507 hIDO2 inhibitorGNF-PF-3777 (8-Nitrotryptanthrin) is a potent human indoleamine 2,3-dioxygenase 2 (hIDO2) inhibitor which significantly reduces IDO2 activity with Ki of 0.97 μM. 了解更多 -
IACS-8968 R-enantiomer
Catalog No. A21555 dual IDO/TDO inhibitorIACS-8968 (R-enantiomer) is the R-enantiomer of IACS-8968. IACS-8968 is a dual IDO and TDO inhibitor, with pIC50s of 6.43 for IDO and <5 for TDO, respectively. 了解更多 -
IACS-8968 S-enantiomer
Catalog No. A21559 dual IDO/TDO inhibitorIACS-8968 (S-enantiomer) is the S-enantiomer of IACS-8968. IACS-8968 is a dual IDO and TDO inhibitor, with pIC50s of 6.43 for IDO and <5 for TDO, respectively. 了解更多 -
INCB024360 analog
Catalog No. A13004 -
Indoximod (NLG-8189)
Catalog No. A14397 -
NLG919
Catalog No. A14322 -
BMS-986205
Catalog No. A17013 IDO1 抑制剂BMS-986205,也称为Linrodostat,ONO-7701和F001287,一种有效且选择性的口服IDO1抑制剂,具有潜在的免疫调节和抗肿瘤活性。 了解更多 -
Bexarotene (LGD1069)
Catalog No. A11094 Retinoid X Receptor LigandBexarotene (LGD1069)是一种高度选择性的类维生素A X受体(RXR)激动剂。 了解更多 -
Adarotene (ST1926)
Catalog No. A11298 Adarotene (ST1926)Adarotene 是一种有效的 apoptosis 诱导剂,通过产生 DNA 损伤,来阻止人类肿瘤细胞的增殖。 了解更多 -
Fenretinide
Catalog No. A12163 -
LG 100268
Catalog No. A14127 -
Tretinoin
Catalog No. A10944 -
Tamibarotene
Catalog No. A11589 RARα 激动剂Tamibarotene是一种是视黄酸受体α/β (RARα/β)的激动剂,在体外可诱导HL-60细胞分化(ED50 = 0.79 nM)和凋亡。 了解更多 -
AGN 194310
Catalog No. A16292 -
AGN 195183
Catalog No. A16293 -
AGN 196996
Catalog No. A16294 RARα 拮抗剂AGN 196996是一种有效的选择性RARα拮抗剂,Ki值为2 nM。对RARβ(Ki = 1087 nM)和RARγ(Ki = 8523 nM)的结合亲和力很小。 了解更多 -
AGN 205327
Catalog No. A16295 -
AGN 205728
Catalog No. A16296