购物车 0 ￥ 0.00
微信关注
申请试用装
  • 主页 /
  • 搜索结果：“ehop 016”

“ehop 016”的搜索结果

37 个项目

每页

设置降序顺序
  1. EHop-016
    Quick View

    EHop-016

    Catalog No. A12740
    Quick View
    Rac GTPase Inhibitor
    EHop-016 is a potent and specific inhibitor of Rac1 and Rac3 GTPase activity that inhibits Vav2 interaction with Rac, Rac-activated PAK1, lamellipodia formation, and cell migration. 了解更多
  2. NMS-P515
    Quick View

    NMS-P515

    Catalog No. A18449
    Quick View
    PARP-1 抑制剂
    NMS-P515 is a potent inhibitor of PARP-1 both in biochemical (Kd: 0.016 μM) and cellular (IC50: 0.027 μM) assays. 了解更多
  3. MethADP sodium salt
    Quick View

    MethADP sodium salt

    Catalog No. A21603
    Quick View
    CD73 inhibitor
    MethADP (sodium salt) is a specific CD73 inhibitor. 了解更多
  4. CRA-026440
    Quick View

    CRA-026440

    Catalog No. A12179
    Quick View
    HDAC inhibitor
    CRA-026440 is a potent, broad-spectrum HDAC inhibitor. 了解更多
  5. Glycolic acid oxidase inhibitor 1
    Quick View

    Glycolic acid oxidase inhibitor 1

    Catalog No. A13016
    Quick View
    glycolate oxidase inhibitor
    Glycolic acid oxidase inhibitor 1 is a glycolate oxidase inhibitor, extracted from patent EP0021228A1, in Table IV. 了解更多
  6. T56-LIMKi
    Quick View

    T56-LIMKi

    Catalog No. A12266
    Quick View
    LIMK2 inhibitor
    T56-LIMKi is a selective inhibitor of LIMK2; inhibits the growth of Panc-1 cells with an IC50 of 35.2 μM. 了解更多
  7. EC330
    Quick View

    EC330

    Catalog No. A13799
    Quick View
    leukemia inhibitory factor (LIF) inhibitor
    EC330 is a leukemia inhibitory factor (LIF) inhibitor. 了解更多
  8. HPGDS inhibitor 2
    Quick View

    HPGDS inhibitor 2

    Catalog No. A18390
    Quick View
    H-PGDS 抑制剂
    HPGDS inhibitor 2 is a highly potent and selective hematopoietic prostaglandin D synthase (H-PGDS) inhibitor with an IC50 of 9.9 nM. 了解更多
  9. Bromodomain IN-1
    Quick View

    Bromodomain IN-1

    Catalog No. A18845
    Quick View
    Bromodomain inhibitor
    Bromodomain IN-1 is a Bromodomain inhibitor extracted from patent WO2016069578A1, compound 4 . 了解更多
  10. UPGL00004
    Quick View

    UPGL00004

    Catalog No. A19047
    Quick View
    GAC inhibitor
    UPGL00004 is a potent allosteric glutaminase C (GAC) inhibitor (IC50=29 nM; Kd=27 nM). UPGL00004 strongly inhibits the proliferation of highly aggressive triple-negative breast cancer cell lines. 了解更多
  11. RV01
    Quick View

    RV01

    Catalog No. A19104
    Quick View
    ALDH2 inhibitor
    RV01 is an analogue of resveratrol, inhibits DNA damage, reduces acetaldehyde dehydrogenase 2 (ALDH2) mRNA expression induced by ethanol, and exhibits hydroxyl radical scavenging activity. RV01 decreases iNOS expression, with anti-neuroinflammatory activity. 了解更多
  12. Fosfomycin calcium
    Quick View

    Fosfomycin calcium

    Catalog No. A18154
    Quick View
    MurA and isopentenyl mevalonate kinase inhibitor
    Fosfomycin calcium is a MurA and isopentenyl mevalonate kinase inhibitor that prevents synthesis of bacterial cell walls. 了解更多
  13. MIK665
    Quick View

    MIK665

    Catalog No. A18362
    Quick View
    Mcl-1 inhibitor
    MIK665 (S-64315) is a special Mcl-1 inhibitor extracted from patent WO2016207225A1, compound Preparation 13, has an IC50 of 1.81 nM. 了解更多
  14. Vadadustat
    Quick View

    Vadadustat

    Catalog No. A16794
    Quick View
    HIF prolyl-hydroxylase 抑制剂
    Vadadustat，也称为AKB-6548和PG-1016548，是一种有效的缺氧诱导因子脯氨酸双加氧酶抑制剂。 了解更多
  15. Sivelestat sodium hydrate (ONO-5046 sodium hydrate)
    Quick View

    Sivelestat sodium hydrate (ONO-5046 sodium hydrate)

    Catalog No. A16137
    Quick View
    Neutrophil elastase 抑制剂
    Sivelestat sodium hydrate (ONO-5046 sodium hydrate)是人嗜中性粒细胞弹性蛋白酶的竞争性抑制剂，还抑制从兔，大鼠，仓鼠和小鼠获得的白细胞弹性蛋白酶。 了解更多
  16. LY2801653 (Merestinib)
    Quick View

    LY2801653 (Merestinib)

    Catalog No. A12557
    Quick View
    c-MET 抑制剂
    LY2801653 (Merestinib)是一种有效的，口服生物利用的小分子c-MET激酶抑制剂（Ki = 2 nM）。 了解更多
  17. KT 5720
    Quick View

    KT 5720

    Catalog No. A16016
    Quick View
    PKA 抑制剂
    KT5720 是一种能透过细胞的、有效的、特异性的、可逆的、ATP 竞争性的蛋白酶 K (PKA) 的抑制剂，其 Ki 值为 60 nM。 了解更多
  18. PD0166285
    Quick View

    PD0166285

    Catalog No. A15863
    Quick View
    Wee1 抑制剂
    PD0166285是一种有效的Wee1和Chk1抑制剂，在纳摩尔浓度下具有活性。PD0166285是一种新型的G2检查点消除剂。 了解更多
  19. ORY-1001 (RG-6016)
    Quick View

    ORY-1001 (RG-6016)

    Catalog No. A15893
    Quick View
    LSD1 抑制剂
    ORY-1001 (RG-6016)是一种活性的选择性赖氨酸脱甲基酶LSD1/KDM1A抑制剂，IC50 <20 nM，对相关FAD依赖性氨氧化酶具有高选择性。 了解更多
  20. ETC-1002
    Quick View

    ETC-1002

    Catalog No. A15815
    Quick View
    ACL 抑制剂 and AMPK 激活剂
    ETC-1002是一种新颖的，一流的可以降低LDL-C的小分子；肝AMP激活的蛋白激酶（AMPK）的激活剂;对肝ATP-柠檬酸裂解酶也具有有效的抑制活性（IC50 = 29 uM）。 了解更多
  21. JH-II-127
    Quick View

    JH-II-127

    Catalog No. A15777
    Quick View
    LRRK2 抑制剂
    JH-II-127是一种高效，选择性和脑渗透性的LRRK2抑制剂，对于LRRK2野生型，LRRK2-G2019S和LRRK2-A2016T，IC50为6.6 nM，2.2 nM和47.7 nM。 了解更多
  22. SU6656
    Quick View

    SU6656

    Catalog No. A15518
    Quick View
    SRC 抑制剂
    SU6656是Src激酶的选择性抑制剂，包括Src，Yes，Lyn和Fyn（分别为IC50 = 280、20、130、170 nM）。 了解更多
  23. NVP DPP 728 dihydrochloride
    Quick View

    NVP DPP 728 dihydrochloride

    Catalog No. A15320
    Quick View
    DPP-4 抑制剂
    NVP DPP 728 dihydrochloride是一种有效的活性二肽基肽酶(DPP)-IV抑制剂，Ki和IC50值分别为11 nM和14 nM。 了解更多
  24. LY2801653 dihydrochloride
    Quick View

    LY2801653 dihydrochloride

    Catalog No. A15150
    Quick View
    MET 抑制剂
    LY2801653 dihydrochloride是一种有效的，口服可生物利用的c-MET激酶小分子抑制剂（Ki = 2 nM）。 了解更多
  25. SR 11302
    Quick View

    SR 11302

    Catalog No. A14950
    Quick View
    AP-1 transcription factor 抑制剂
    SR 11302，活化蛋白1（AP-1）转录因子活性的抑制剂，在体内表现出抗肿瘤作用。 了解更多
  26. Deoxygalactonojirimycin HCl
    Quick View

    Deoxygalactonojirimycin HCl

    Catalog No. A14016
    Quick View
    Alpha-galactosidase 抑制剂
    Deoxygalactonojirimycin Hydrochloride是一种有效且选择性的Alpha-gal A（Alpha-半乳糖苷酶）抑制剂。 了解更多
  27. BV-6
    Quick View

    BV-6

    Catalog No. A14231
    Quick View
    dual cIAP and XIAP 抑制剂
    BV-6是一种SMAC模拟，双重cIAP和XIAP抑制剂。 了解更多
  28. KX2-391
    Quick View

    KX2-391

    Catalog No. A11177
    Quick View
    Src 抑制剂
    KX2-391是新型的非ATP竞争底物口袋定向SRC抑制剂。 了解更多
  29. SB939 ( Pracinostat )
    Quick View

    SB939 ( Pracinostat )

    Catalog No. A10830
    Quick View
    HDAC 抑制剂
    SB939 (Pracinostat)是HDAC的口服抑制剂，对I，II和IV类HDAC具有选择性，在体外HDAC1活性测定中显示IC50值为77 nM。 了解更多
  30. BS-181
    Quick View

    BS-181

    Catalog No. A10163
    Quick View
    CDK 抑制剂
    BS-181 是作为CDK7抑制剂的潜在抗肿瘤剂。 了解更多
  31. Bosutinib (SKI-606)
    Quick View

    Bosutinib (SKI-606)

    Catalog No. A10161
    Quick View
    Src 抑制剂
    Bosutinib (SKI-606)是一种酪氨酸激酶抑制剂。 了解更多
  32. Brivanib alaninate (BMS-582664)
    Quick View

    Brivanib alaninate (BMS-582664)

    Catalog No. A10162
    Quick View
    VEGFR 抑制剂
    Brivanib alaninate (BMS-582664)是VEGFR和FGFR信号转导的双重酪氨酸激酶抑制剂。 了解更多
  33. YM201636
    Quick View

    YM201636

    Catalog No. A11064
    Quick View
    PI3K 抑制剂
    YM201636是PIKfyve的细胞渗透性和选择性抑制剂（IC50 = 33 nM）。 了解更多
  34. BSI-201 (Iniparib)
    Quick View

    BSI-201 (Iniparib)

    Catalog No. A10164
    Quick View
    PARP 抑制剂
    BSI-201 (Iniparib)是一种有效的PARP-1抑制剂，已被证明可以穿越血脑屏障。 了解更多
  35. BTZ043 (BTZ038, BTZ044) Racemate
    Quick View

    BTZ043 (BTZ038, BTZ044) Racemate

    Catalog No. A10165
    Quick View
    DprE1 抑制剂
    BTZ043 (BTZ038,BTZ044) Racemate 抑制癸二烯基磷酸基-β-d-核糖2α-表异构酶，它是一种产生致病细菌结核分枝杆菌细胞壁的酶。 了解更多
  36. Bortezomib (Velcade)
    Quick View

    Bortezomib (Velcade)

    Catalog No. A10160
    Quick View
    Proteasome 抑制剂
    Bortezomib (Velcade)是26S蛋白酶体的高度选择性，可逆抑制剂。 了解更多
  37. BKM120 (NVP-BKM120, Buparlisib)
    Quick View

    BKM120 (NVP-BKM120, Buparlisib)

    Catalog No. A11016
    Quick View
    PI3K 抑制剂?
    BKM120 (NVP-BKM120,Buparlisib)是生物可利用的口服泛I类磷脂酰肌醇3激酶（PI3K）激酶抑制剂，在无细胞试验中作用于p110α/β/δ/γ的。对VPS34，mTOR，DNAPK的作用效果下降，而对 PI4Kβ几乎没有活性。 了解更多

37 个项目

每页

设置降序顺序
联系我们
ChinaChina

Adooq 中国 (南京百鑫德诺生物科技有限公司)

免费电话: 400-025-6535

企业QQ: 400-025-6535

www.adooq.cn

sales@adooq.cn

United StatesUnited States

Adooq Bioscience

Toll Free: (866) 930-6790

Fax: +1-323-606-8156

Email: sales@adooq.com

Not your Region? View all Distributors

FILTER BY:

Filtering:

  1. 作用机制: Inhibitor (抑制剂) 删除该内容
清除全部

购物选项

分类
  1. Epigenetics (6)
  2. Apoptosis (1)
  3. PI3K / Akt / mTOR (3)
  4. Protein Tyrosine Kinases (6)
  5. Angiogenesis (2)
  6. MAPK (1)
  7. Cell Cycle (4)
  8. DNA Damage (4)
  9. Cell Metabolism (1)
  10. Autophagy Signaling (1)
  11. Immunology & Inflammation (1)
  12. NF-kB/IkB (2)
  13. TGF-β / Smad (2)
  14. Proteases (3)
  15. Others (2)
  16. Ready to Use Solution (9)
  17. Products On Sale (12)
靶点
  1. cIAP (1)
  2. FGFR1 (1)
  3. HDAC (1)
  4. KDM1A (LSD1) (1)
  5. PARP1 (1)
  6. VEGFR1 (FLT1) (1)
  7. VEGFR2 (FLK1) (1)
  8. XIAP (1)
ADOOQ 产品质量保证
Guaranteed product quality, 365 days Unconditional Return & Replacement

We promise all products to perform as described.

立即申请
Get Code
联系我们
查看FAQs

Adooq 公司

产品订购

技术资源

地址

© 2006-2019 AdooQ BioScience （南京百鑫德诺生物科技有限公司）. All Rights Reserved.
苏ICP备14027875号
Accept Payment
Rewards