Cell Metabolism

产品 401 到 450 共 623个

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  1. AMG-333

    Catalog No. A17182
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    TRPM8 拮抗剂
    AMG-333是有效的选择性TRPM8拮抗剂,IC50为13 nM。 了解更多
  2. PX20606 trans-isomer

    Catalog No. A16997
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    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
  3. Mutant IDH1 inhibitor

    Catalog No. A21150
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    mutant IDH1 R132H inhibitor
    Mutant IDH1 inhibitor is a potent mutant IDH1 R132H inhibitor with IC50 of < 72 nM. 了解更多
  4. Mutant IDH1-IN-2

    Catalog No. A21339
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    IDH inhibitor
    Mutant 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
  5. Mutant IDH1-IN-1

    Catalog No. A21359
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    mutant-selective IDH1 inhibitor
    Mutant 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
  6. AGI-5198 (IDH-C35)

    Catalog No. A12902
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    IDH1 抑制剂
    AGI-5198 (IDH-C35)是一种非常有效的选择性IDH1突变抑制剂,具有潜在的抗癌活性。 了解更多
  7. AGI-6780

    Catalog No. A12903
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    IDH2 R140Q 抑制剂
    AGI-6780是有效的选择性IDH2突变抑制剂,IC50值为23 nM。 了解更多
  8. IDH-C227

    Catalog No. A12923
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    IDH1 R132H 抑制剂
    IDH-C227是一种有效的选择性IDH1 R132H抑制剂。 了解更多
  9. Enasidenib

    Catalog No. A15808
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    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
  10. AG-120 (Ivosidenib)

    Catalog No. A14386
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    IDH1 抑制剂
    AG-120 (Ivosidenib)是1型异柠檬酸脱氢酶(IDH1)的口服抑制剂,具有潜在的抗肿瘤活性。 了解更多
  11. IDH-305

    Catalog No. A16943
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    IDH1 抑制剂
    IDH305是柠檬酸循环酶异柠檬酸脱氢酶[NADP]细胞质的抑制剂(异柠檬酸脱氢酶1,IDH1),在残基R132(IDH1(R132))处具有突变,具有潜在的抗肿瘤活性。 了解更多
  12. Vorasidenib

    Catalog No. A16908
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    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
  13. BAY-1436032

    Catalog No. A17059
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    mIDH1 抑制剂
    BAY-1436032是一种有效的,选择性的,口服的突变型异柠檬酸脱氢酶1(mIDH1)抑制剂。 了解更多
  14. Olutasidenib (FT-2102)

    Catalog No. A18789
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    IDH1 inhibitor
    Olutasidenib is a potent, selective inhibitor of mutant Isocitrate dehydrogenase (IDH)1 for the treatment of acute myeloid leukemia. 了解更多
  15. Mutant IDH1-IN-4

    Catalog No. A19106
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    IDH1 inhibitor
    Mutant 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
  16. IDH1 Inhibitor 2

    Catalog No. A18420
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    IDH1 inhibitor
    DH1 Inhibitor 2 is a potent IDH1 inhibitor via a direct covalent modification of His315, with an IC50 of 110 nM. 了解更多
  17. Epacadostat (INCB024360)

    Catalog No. A15554
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    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
  18. IDO/TDO-IN-1

    Catalog No. A18566
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    IDO/TDO dual inhibitor
    IDO/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
  19. IDO-IN-12

    Catalog No. A18988
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    IDO inhibitor
    IDO-IN-12 is an indoleamine 2,3-dioxygenase (IDO) inhibitor extracted from patent WO 2017181849 A1. 了解更多
  20. GNF-PF-3777

    Catalog No. A13507
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    hIDO2 inhibitor
    GNF-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
  21. IDO-IN-3

    Catalog No. A20898
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    IDO inhibitor
    IDO-IN-3 is a potent indoleamine 2,3-dioxygenase (IDO) inhibitor with an IC50 of 290 nM. 了解更多
  22. IDO-IN-5

    Catalog No. A21074
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    IDO inhibitor
    IDO-IN-5 (NLG-1489) is an indoleamine 2,3-dioxygenase (IDO) inhibitor extracted from patent WO WO2012142237A1, compound 1489, has an IC50 of 1-10 μM. 了解更多
  23. IDO-IN-4

    Catalog No. A21077
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    IDO-1 inhibitor
    IDO-IN-4 is an indoleamine 2,3-dioxygenase 1 (IDO-1) inhibitor, extracted from patent WO2014150677A1, Compound example 1 enantiomer 1. 了解更多
  24. IACS-8968 R-enantiomer

    Catalog No. A21555
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    dual IDO/TDO inhibitor
    IACS-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
  25. IACS-8968 S-enantiomer

    Catalog No. A21559
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    dual IDO/TDO inhibitor
    IACS-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
  26. INCB024360 analog

    Catalog No. A13004
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    IDO1 抑制剂
    INCB024360 analog是一种羟胺和吲哚胺2,3-二加氧酶(IDO1)抑制剂,具有潜在的免疫调节和抗肿瘤活性。 了解更多
  27. Indoximod (NLG-8189)

    Catalog No. A14397
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    IDO 抑制剂
    Indoximod (NLG-8189)是具有抗免疫抑制活性的甲基化色氨酸。 了解更多
  28. NLG919

    Catalog No. A14322
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    IDO 抑制剂
    NLG919是一种吲哚胺2,3-二加氧酶1(IDO1)的口服抑制剂,具有潜在的免疫调节和抗肿瘤活性。 了解更多
  29. BMS-986205

    Catalog No. A17013
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    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
  30. AC-55649

    Catalog No. A20078
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    Human RARβ2 receptor agonist
    AC-55649 is a potent, highly isoform-selective agonist of human RARβ2 receptor, with a pEC50 of 6.9. 了解更多
  31. WYC-209

    Catalog No. A19001
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    RAR agonist
    WYC-209, a synthetic retinoid, is a retinoic acid receptor (RAR) agonist. 了解更多
  32. Bexarotene (LGD1069)

    Catalog No. A11094
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    Retinoid X Receptor Ligand
    Bexarotene (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
  33. 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
  34. Acitretin

    Catalog No. A10035
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    Acitretin是第二代类维生素A,通常用于牛皮癣。 了解更多
  35. Adapalene

    Catalog No. A10038
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    Adapalene是一类RAR和RXR双重的激动剂,主要用于治疗痤疮。 了解更多
  36. AM 580

    Catalog No. A11792
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    RARα 激动剂
    AM 580是视黄酸的类似物,可作为选择性RARα激动剂。 了解更多
  37. CD 437

    Catalog No. A11793
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    RARγ-selective 激动剂
    CD 437是一种合成类维生素A,是一种RARγ选择性激动剂。 了解更多
  38. Tazarotene

    Catalog No. A10894
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    Tazarotene是前药和类维生素A的炔类的成员。 了解更多
  39. Palovarotene

    Catalog No. A12430
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    Palovarotene是一种治疗肺气肿的新型维甲酸受体γ激动剂。 了解更多
  40. AR7

    Catalog No. A12905
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    RARα 拮抗剂.
    AR7是视黄酸受体α(RARα)拮抗剂。 了解更多
  41. TTNPB

    Catalog No. A13007
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    RAR 激动剂
    TTNPB增强了化学诱导的多能干细胞(CiPSC)的重编程效率。 了解更多
  42. Fenretinide

    Catalog No. A12163
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    RAR 激动剂
    Fenretinide是一种合成类视黄醇激动剂。它是一种体内半衰期长的抗增殖、抗氧化和抗癌药物。 了解更多
  43. LG 100268

    Catalog No. A14127
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    RXR 激动剂
    LG 100268是一种有效的RXR激动剂,可用于评估非胰岛素依赖型(II型)糖尿病(NIDDM)。 了解更多
  44. Tretinoin

    Catalog No. A10944
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    RAR 激动剂
    Tretinoin 是视黄酸受体的内源性激动剂,RAR-α,RAR-β和RAR-γ受体的IC50值为14 nM。 了解更多
  45. Tamibarotene

    Catalog No. A11589
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    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
  46. AGN 194310

    Catalog No. A16292
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    pan-RARs 激动剂
    AGN 194310是一种有效的选择性Pan-RARs激动剂,对于RARα/β/γ的Kd值分别为3/2/5 nM。 了解更多
  47. AGN 195183

    Catalog No. A16293
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    RARα 激动剂
    AGN 195183是RARα(Kd = 3 nM)的强效选择性激动剂,相对于AGN 193836具有增强的结合选择性。对RARβ/γ无活性。 了解更多
  48. AGN 196996

    Catalog No. A16294
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    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
  49. AGN 205327

    Catalog No. A16295
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    RAR 激动剂
    AGN 205327是一种有效的合成RARs激动剂,对RARα/β/γ的EC50分别为3766/734/32 nM;对RXR无抑制作用。 了解更多
  50. AGN 205728

    Catalog No. A16296
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    RARγ 拮抗剂
    AGN 205728是一种有效的选择性RARγ拮抗剂,Ki/IC95值为3 nM/0.6 nM;对RARα和RARβ无抑制作用。 了解更多

产品 401 到 450 共 623个

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