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  1. (Rac)-AZD 6482

    Catalog No. A20629
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    p110β inhibitor
    Rac)-AZD 6482 ((Rac)-KIN-193) is a less active racemate of AZD 6482. AZD 6482 is a potent and selective p110β inhibitor with an IC50 of 0.69 nM. 了解更多
  2. AZD-5991 S-enantiomer

    Catalog No. A21361
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    Mcl-1 inhibitor
    AZD-5991 S-enantiomer is the less active enantiomer of AZD-5991. AZD-5991 S-enantiomer is a Mcl-1 inhibitor with an IC50 of 6.3 μM in FRET assay and a Kd of 0.98 μM in surface plasmon resonance (SPR) assay. 了解更多
  3. AZD-5991 Racemate

    Catalog No. A21357
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    Mcl-1 inhibitor
    AZD-5991 Racemate is the racemate of AZD-5991. AZD-5991 Racemate is a Mcl-1 inhibitor with an IC50 of <3 nM in FRET assay. 了解更多
  4. AZD-0284

    Catalog No. A18766
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    RORγ 激动剂
    AZD-0284 is a potent, selective, inverse agonist of the nuclear receptor RORγ for the potential treatment of Plaque psoriasis. 了解更多
  5. AZD-4320

    Catalog No. A17171
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    Bcl-2/Bcl-XL 抑制剂
    AZD-4320是BH3模拟物和双重Bcl-2/Bcl-XL抑制剂。AZD4320 对于 KPUM-MS3,KPUM-UH1,和 STR-428 细胞系的 IC50 分别为 26 nM,17 nM,和 170 nM。 了解更多
  6. AZD-5904

    Catalog No. A17062
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    MPO 抑制剂
    AZD-5904是一种有效的生物利用MPO抑制剂。在临床前研究中,AZD-5904以140 nM的IC50抑制了分离出的MPO酶,在大鼠和小鼠MPO酶活性的测定中具有大约等价性。 了解更多
  7. AZD-6280

    Catalog No. A20684
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    GABAA(α2/3) receptor modulator
    AZD-6280 is a selective GABAA(α2/3) receptor modulator, used for treatment of generalized anxiety disorder. 了解更多
  8. AZD 9272

    Catalog No. A19738
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    mGluR5 antagonist
    AZD 9272 is a brain penetrant mGluR5 antagonist. 了解更多
  9. AZD 2066

    Catalog No. A19729
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    mGluR5 antagonist
    AZD 2066 is a selective, orally active and brain-penetrant mGluR5 antagonist, with analgesia activity. 了解更多
  10. AZD-9291 (Osimertinib)

    Catalog No. A13681
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    EGFR 抑制剂
    AZD-9291 (Osimertinib)是第三代EGFR抑制剂,在临床前研究中显示出希望,并为已对现有EGFR抑制剂产生耐药性的晚期肺癌患者提供了希望。 了解更多
  11. AZD-2461

    Catalog No. A12393
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    PARP 抑制剂
    AZD2461是新型有效的PARP抑制剂,对P-糖蛋白的亲和力较低。 了解更多
  12. AZD-8529

    Catalog No. A20045
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    mGluR2 modulator
    AZD-8529 is a potent, highly selective and orally bioavailable positive allosteric modulator of mGluR2, with an EC50 of 285 nM, and shows no positive allosteric modulator responses at 20-25 M on the mGluR1, 3, 4, 5, 6, 7, and 8 subtypes. 了解更多
  13. AZD-7648

    Catalog No. A20049
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    DNA-PK inhibitor
    AZD-7648 is a potent and selective DNA-PK inhibitor. Anti-tumor activity. 了解更多
  14. AZD-4635 (HTL1071)

    Catalog No. A16820
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    A2AR 拮抗剂
    AZD-4635 (HTL1071)是一种口服A2AR拮抗剂,可与人A2AR结合,Ki为1.7 nM,选择性比其他腺苷受体高30倍。 了解更多
  15. AZD-5069

    Catalog No. A15941
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    CXCR2 拮抗剂
    AZD-5069是一种有效的选择性CXCR2拮抗剂,具有抑制COPD患者中性粒细胞向气管迁移的潜能。 了解更多
  16. AZD-3965

    Catalog No. A14186
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    MCT1 抑制剂
    AZD-3965(AZD3965)是具有1.6 nM结合亲和力的单羧酸盐转运蛋白1(MCT1)的选择性抑制剂,是MCT2的6倍选择性,在10μM时不抑制MCT4。 了解更多
  17. AZD 7545

    Catalog No. A14157
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    PDHK 抑制剂
    AZD7545是PDHK2的新型选择性小分子抑制剂(PDH激酶2),对PDHK1和PDHK2的IC50分别为36.8 nM和6.4 nM。 了解更多
  18. AZD 2932

    Catalog No. A14156
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    mutil-targeted protein tyrosine kinase 抑制剂
    AZD2932是一种有效且靶向多用途的蛋白酪氨酸激酶抑制剂,对VEGFR-2,PDGFRβ,Flt-3和c-Kit的IC50分别为8 nM,4 nM,7 nM和9 nM。 了解更多
  19. Volitinib (Savolitinib, AZD-6094)

    Catalog No. A14419
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    c-Met 抑制剂
    Volitinib (Savolitinib,AZD-6094)是c-Met受体酪氨酸激酶的生物利用抑制剂,具有潜在的抗肿瘤活性。 了解更多
  20. Osimertinib dimesylate

    Catalog No. A18243
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    EGFR inhibitor
    Osimertinib dimesylate (AZD-9291 dimesylate) is an irreversible and mutant selective EGFR inhibitor with IC50s of 12 and 1 nM against EGFRL858R and EGFRL858R/T790M, respectively. 了解更多
  21. Cediranib maleate

    Catalog No. A21857
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    VEGFR inhibitor
    Cediranib maleate (AZD-2171 maleate) is a highly potent, orally available VEGFR inhibitor with IC50s of <1, <3, 5, 5, 36, 2 nM for Flt1, KDR, Flt4, PDGFRα, PDGFRβ, c-Kit, respectively. 了解更多
  22. Glycine

    Catalog No. A17936
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    NMDA antagonist
    AZD-4282, also known as aminoacetic acid and glycine, is a N-methyl-D-aspartate (NMDA) receptor antagonist potentially for the treatment of neuropathic pain. 了解更多
  23. AZD5991

    Catalog No. A16880
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    Mcl-1 抑制剂
    AZD-5991是一种有效的选择性Mcl-1抑制剂,在FRET分析中的IC50为0.7 nM,在表面等离子体共振(SPR)分析中的Kd为0.17 nM。 了解更多
  24. Ispronicline (TC-1734, AZD-3480)

    Catalog No. A14183
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    nAChR 激动剂
    Ispronicline (TC-1734,AZD-3480)是神经元烟碱乙酰胆碱受体部分激动剂。Ispronicline是亚型选择性的,主要与a4b2亚型结合。它具有抗抑郁、益智和神经保护作用。 了解更多
  25. AZD6482 (S-isomer)

    Catalog No. A22606
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    PI3Kβ inhibitor
    AZD6482 (S-isomer), CAS#1173900-37-2, is an isomer of AZD6482 (MedKoo Cat#406268) with S-configuration. AZD6482 is a potent, selective and ATP competitive PI3Kβ inhibitor (IC(50) 0.01 μm). 了解更多
  26. Verdiperstat (AZD3241)

    Catalog No. A22041
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    MPO inhibitor
    Verdiperstat (AZD3241) is a selective, irreversible and orally active myeloperoxidase (MPO) inhibitor, with an IC50 of 630 nM, and can be used in the research of neurodegenerative brain disorders. 了解更多
  27. Zoliflodacin

    Catalog No. A22032
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    DNA gyrase/topoisomerase inhibitor
    Zoliflodacin (ETX0914;AZD0914) is a novel spiropyrimidinetrione bacterial DNA gyrase/topoisomerase inhibitor. 了解更多
  28. Linaprazan

    Catalog No. A20526
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    Linaprazan (AZD0865) inhibits gastric H+,K+-ATPase by K+-competitive binding. (IC50: 1.0 ± 0.2 μM) It is a acid-suppressing agents with rapid onset of action and potent acid inhibition. 了解更多
  29. AZD7594

    Catalog No. A19866
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    glucocorticoid receptor modulator
    AZD7594 is a potent selective nonsteroidal glucocorticoid receptor modulator, with an IC50 of 0.9 nM. 了解更多
  30. AZD7624

    Catalog No. A19849
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    inhaled p38 inhibitor
    AZD7624 is an inhaled p38 inhibitor, with potent anti-inflammatory activity. 了解更多
  31. AZD0424

    Catalog No. A19488
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    Src/Abl kinase inhibitor
    AZD0424 is an orally active, and dual selective Src/Abl kinase inhibitor with potential antineoplastic activity. AZD0424 induces apoptosis and cell cycle arrest in lymphoma cells. 了解更多
  32. Lanicemine

    Catalog No. A19339
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    NMDA channel blocker
    Lanicemine (AZD6765) is a low-trapping NMDA channel blocker with a binding (Ki) of 0.56-2.1?μM. 了解更多
  33. AZD3229

    Catalog No. A19259
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    pan-KIT mutant inhibitor
    AZD3229 is a potent pan-KIT mutant inhibitor for the treatment of gastrointestinal stromal tumors. 了解更多
  34. Elobixibat

    Catalog No. A20984
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    (IBAT inhibitor
    Elobixibat is a potent ileal bile acid transporter (IBAT) inhibitor with IC50 values of 0.53 ?? 0.17 nM, 0.13 ?? 0.03 nM, and 5.8 ?? 1.6 nM for human IBAT, mouse IBAT, and canine IBAT. 了解更多
  35. AZD5153 6-Hydroxy-2-naphthoic acid

    Catalog No. A21852
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    BET/BRD4 bromodomain inhibitor
    AZD5153 6-Hydroxy-2-naphthoic acid is the 6-Hydroxy-2-naphthoic acid of AZD5153. AZD5153 is a potent, selective, and orally available BET/BRD4 bromodomain inhibitor; disrupts BRD4 with an IC50 of 1.7 nM. 了解更多
  36. AZD5582

    Catalog No. A21735
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    IAPs antagonist
    AZD5582 is an antagonist of the inhibitor of apoptosis proteins (IAPs), which binds to the BIR3 domains cIAP1, cIAP2, and XIAP with IC50s of 15, 21, and 15 nM, respectively. 了解更多
  37. AZD9496 maleate

    Catalog No. A21726
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    estrogen receptor (ERα) antagonist
    AZD9496 maleate is a potent and selective estrogen receptor (ERα) antagonist with IC50 of 0.28 nM. AZD9496 maleate is an orally bioavailable selective oestrogen receptor degrader (SERD). 了解更多
  38. AZD3839 free base

    Catalog No. A21606
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    BACE1 inhibitor
    AZD3839 (free base) is a potent and selective BACE1 inhibitor with IC50 of 23.6 uM, about 14-fold selectivity over BACE2, also a β-secretase enzyme inhibitor. 了解更多
  39. AZD8329

    Catalog No. A21081
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    11β-HSD1 inhibitor
    AZD8329 is a potent 11β-Hydroxysteroid dehydrogenase type 1 (11β-HSD1) inhibitor with an IC50 of 9 nM for human 11β-HSD1, displays excellent selectivity versus 11β-HSD2, 17β-HSD1 and 17β-HSD3. 了解更多
  40. Lanabecestat

    Catalog No. A12282
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    BACE1 inhibitor
    Lanabecestat (AZD3293) is a potent, highly permeable, orally active and blood-brain barrier penetrating BACE1 inhibitor with a Ki of 0.4 nM. 了解更多
  41. AZD3988

    Catalog No. A13208
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    DGAT-1 inhibitor
    AZD3988 is a diacylglycerol acyl transferase-1 (DGAT-1) inhibitor with IC50s of 6, 5, 11 nM for human, rat, mouse, respectively. 了解更多
  42. AZD2906

    Catalog No. A18936
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    glucocorticoid receptor agonist
    AZD2906 is a selective glucocorticoid receptor (GR) agonist, increases micronucleated immature erythrocytes in the bone marrow of rats. AZD2906 shows IC50s of 2.2, 0.3, 41.6 and 7.5 nM at GR in human, rat PBMC and human, rat whole blood, respectively. 了解更多
  43. AZD9898

    Catalog No. A18959
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    LTC4S inhibitor
    AZD9898 is an orally active leukotriene-C4 synthetase (LTC4S, glutathione S-transferase II) inhibitor, with an IC50 of 0.28 nM. AZD9898 mitigates the GABA binding and hepatic toxicity signal. AZD9898 has the potential to treat asthma. 了解更多
  44. AZD9567

    Catalog No. A18850
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    selective glucocorticoid receptor modulator
    AZD9567 is a potent, oral active, non-steroidal and selective glucocorticoid receptor modulator (SGRM), with an IC50 of 3.8 nM. 了解更多
  45. AZD4573

    Catalog No. A18321
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    CDK9 inhibitor
    AZD4573 is a potent and selective inhibitor of CDK9, with fast-off binding kinetics and high selectivity versus other kinases, including other CDK family kinases. 了解更多
  46. AZD7986

    Catalog No. A17095
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    DPPI 抑制剂
    AZD7986,也称为INS 1007,是第二代可逆共价,有效和选择性DPP1抑制剂,潜在地可用于治疗慢性阻塞性肺疾病(COPD),其预测的人PK特性适用于每日一次人类给药。 了解更多
  47. AZD3229 Tosylate

    Catalog No. A16867
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    pan-KIT mutant 抑制剂
    AZD3229 Tosylate是一种有效的pan-KIT突变抑制剂,用于治疗胃肠道间质瘤。 了解更多
  48. AZD7507

    Catalog No. A16886
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    CSF-1R 抑制剂
    AZD7507是一种有效的选择性CSF-1R抑制剂(32 nM细胞活性),AZD7507被认为是一种很有前途的化合物,因为它保留了AZ683所需的效能和口服药代动力学特性。 了解更多
  49. AZD1208 HCl

    Catalog No. A16927
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    PIM kinases 抑制剂
    AZD1208 HCl是一种新型的,口服可生物利用的高选择性PIM激酶抑制剂。 了解更多
  50. AZD0364

    Catalog No. A16839
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    ERK 抑制剂
    AZD0364是一种临床前ERK1/2抑制剂,对ERK2的IC50为0.6 nM。 了解更多

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