“ab fubinaca”的搜索结果

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  1. Talazoparib tosylate

    Catalog No. A20238
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    PARP1/2 inhibitor
    Talazoparib tosylate (BMN 673ts) is a novel, potent and orally available PARP1/2 inhibitor with an IC50 of 0.57 nM for PARP1. 了解更多
  2. GeA-69

    Catalog No. A19705
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    PARP14 inhibitor
    GeA-69 is a selective, highly cell permeable allosteric inhibitor of poly-adenosine-diphosphate-ribose polymerase 14 (PARP14) targeting macrodomain 2, with a Kd of 2.1 ?M. 了解更多
  3. NMS-P118

    Catalog No. A20994
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    PARP-1 Inhibitor
    NMS-P118 is a potent, orally available, and highly selective PARP-1 Inhibitor for cancer therapy. 了解更多
  4. Veliparib dihydrochloride

    Catalog No. A21356
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    PARP inhibitor
    Veliparib dihydrochloride is a potent PARP inhibitor, inhibiting PARP1 and PARP2 with Kis of 5.2 and 2.9 nM, respectively. 了解更多
  5. HDAC-IN-7

    Catalog No. A21252
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    HDAC1/2/3/10 inhibitor
    HDAC-IN-7 (Chidamide impurity) is an impurity of Chidamide. Chidamide is a potent and orally bioavailable HDAC enzymes class I (HDAC1/2/3) and class IIb (HDAC10) inhibitor. 了解更多
  6. Niraparib hydrochloride

    Catalog No. A18018
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    PARP1 and PARP2 inhibitor
    Niraparib hydrochloride (MK-4827 hydrochloride) is a highly potent and orally bioavailable PARP1 and PARP2 inhibitor with IC50s of 3.8 and 2.1 nM, respectively. 了解更多
  7. Niraparib tosylate

    Catalog No. A16618
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    PARP1/PARP2 inhibitor
    Niraparib tosylate (MK-4827 tosylate) is a highly potent and orally bioavailable PARP1 and PARP2 inhibitor with an IC50 of 3.8 and 2.1 nM, respectively. 了解更多
  8. MAC glucuronide α-hydroxy lactone-linked SN-38

    Catalog No. A18407
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    Topoisomerase I inhibitor
    MAC glucuronide α-hydroxy lactone-linked SN-38 (Topoisomerase I inhibitor) is a stabilized lactone MAC glucuronide α-hydroxy lactone-linked SN-38 drug linker. 了解更多
  9. CHDI-390576

    Catalog No. A18899
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    HDAC inhibitor
    CHDI-390576, a potent, cell permeable and CNS penetrant class IIa histonedeacetylase (HDAC) inhibitor with IC50s of 54 nM, 60 nM, 31 nM, 50 nM for class IIa HDAC4, HDAC5, HDAC7, HDAC9, respectively, shows >500-fold selectivity over class I HDACs (1, 2, 3) and ~150-fold selectivity over HDAC8 and the class IIb HDAC6 isoform. 了解更多
  10. ACX-362E

    Catalog No. A18560
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    DNA polymerase IIIC 抑制剂
    ACX-362E is an orally available DNA polymerase IIIC (pol IIIC) inhibitor, acts as an antimicrobial agent to treat Gram-positive infections, with a MIC50 of 2 μg/mL for C. difficile. ACX-362E displays very potent in vitro and in vivo activities against broad spectrum of C. difficile pathogens. 了解更多
  11. Tucidinostat (Chidamide)

    Catalog No. A17861
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    HDAC inhibitor
    Tucidinostat is a potent and orally bioavailable HDAC enzymes class I (HDAC1/2/3) and class IIb (HDAC10) inhibitor, with IC50s of 95, 160, 67 and 78 nM, less active on HDAC8 and HDAC11 (IC50s, 733 nM, 432 nM, respectively), and shows no effect on HDAC4/5/6/7/9. 了解更多
  12. AZ32

    Catalog No. A16814
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    ATM 抑制剂
    AZ32是ATM激酶的特异性抑制剂,对小鼠具有良好的BBB渗透性,ATM酶的IC50值<0.0062 uM。它对ATR有足够的选择性,并且具有较高的细胞通透性。 了解更多
  13. AN3365

    Catalog No. A16329
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    leucyl-tRNA synthetase 抑制剂
    AN3365是一种有效的,选择性的亮氨酰tRNA合成酶抑制剂。 了解更多
  14. ABT 492 meglumine (Delafloxacin meglumine)

    Catalog No. A15064
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    ABT 492 meglumine (Delafloxacin meglumine)对喹诺酮敏感和耐药的革兰氏阳性生物更有力,对环丙沙星家族肠杆菌科的某些成员具有类似于环丙沙星的活性,对喹诺酮敏感,非发酵性,革兰氏阴性生物具有类似的活性。 了解更多
  15. Tasquinimod

    Catalog No. A12616
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    HDAC4 抑制剂
    Tasquinimod是一种变构抑制HDAC4信号传导的口服活性抗血管生成剂。 了解更多
  16. Rifabutin

    Catalog No. A10790
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    RNA polymerase 抑制剂
    Rifabutin是一种主要用于治疗肺结核的杀菌抗生素。它的作用是基于阻断细菌的DNA依赖性RNA聚合酶。 了解更多
  17. Fludarabine Phosphate (Fludara)

    Catalog No. A10395
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    Fludarabine Phosphate (Fludara)是一种用于治疗血液恶性肿瘤(血细胞癌,如白血病和淋巴瘤)的化疗药物。氟达拉滨通过干扰核糖核苷酸还原酶和dna聚合酶来抑制DNA合成。它对分裂细胞和静止细胞都有活性。 了解更多
  18. Clofarabine

    Catalog No. A10228
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    DNA/RNA Synthesis 抑制剂
    Clofarabine具有抗肿瘤活性的第二代嘌呤核苷类似物。 了解更多
  19. Abacavir

    Catalog No. A11115
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    Transcriptase 抑制剂
    Abacavir是一种核苷类似物逆转录酶抑制剂(NRTI);鸟苷类似物用于治疗艾滋病毒和艾滋病。 了解更多
  20. Abacavir sulfate

    Catalog No. A11120
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    Transcriptase 抑制剂
    Abacavir sulfate是一种核苷类似物逆转录酶抑制剂(NRTI)。 了解更多
  21. Nelarabine (Arranon)

    Catalog No. A10632
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    Nelarabine是一种嘌呤核苷类似物,可转化为其相应的阿拉伯糖基鸟嘌呤核苷酸三磷酸(araGTP),从而抑制DNA合成和细胞毒性,IC50为0.067-2.15 μM。 了解更多
  22. PP121

    Catalog No. A11207
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    PI3K 抑制剂
    PP121是一种作用于PDGFR,Hck,mTOR,VEGFR2,Src和Abl的多靶点抑制剂,IC50分别为2 nM,8 nM,10 nM,12 nM,14 nM和18 nM,也抑制DNA-PK,IC50为60 nM。 了解更多
  23. ABT-492 (Delafloxacin)

    Catalog No. A10023
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    Fluoroquinolone antibiotic
    ABT-492 (Delafloxacin)是一种新的氟喹诺酮类药物,可抵抗155种需氧和171种厌氧菌。 了解更多
  24. Gemcitabine HCl (Gemzar)

    Catalog No. A10423
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    DNA/RNA Synthesis 抑制剂
    Gemcitabine HCl (Gemzar)是一种DNA synthesis抑制剂,作用于PANC1,MIAPaCa2,BxPC3和Capan2细胞,通过在癌细胞dna复制过程中取代核酸的一个组成部分,防止肿瘤生长。 了解更多
  25. PCI-24781 (Abexinostat)

    Catalog No. A10700
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    HDAC 抑制剂
    PCI-24781 (Abexinostat)是一种广谱苯基异羟肟酸HDAC抑制剂。 了解更多
  26. 3-Aminobenzamide

    Catalog No. A10475
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    PARP 抑制剂
    3-Aminobenzamide是一种新型PARP抑制剂,已知它通过抑制DNA损伤的修复使细胞在体外对辐射敏感。 了解更多
  27. ABT-888 (Veliparib)

    Catalog No. A10026
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    PARP 抑制剂
    ABT-888 (Veliparib)是一种潜在的抗癌药物,可作为PARP抑制剂。 了解更多

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