“ehop 016”的搜索结果

产品 51 到 100 共 123个

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  1. HAX1 Human

    Catalog No. AP0623
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    HCLS1 Associated Protein X-1 Human Recombinant 了解更多
  2. RPS2 Human

    Catalog No. AP1016
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    Ribosomal Protein S2 Human Recombinant 了解更多
  3. THYN1 Human

    Catalog No. AP1748
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    Thymocyte Nuclear Protein 1 Human Recombinant 了解更多
  4. DR1 Human

    Catalog No. AP1966
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    Down-Regulator of Transcription 1 Human Recombinant 了解更多
  5. CST3 Mouse

    Catalog No. AP2016
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    Cystatin-C Mouse Recombinant 了解更多
  6. SNAP23 Human

    Catalog No. AP2074
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    Synaptosomal-associated protein 23 Human Recombinant 了解更多
  7. CYB5A Human

    Catalog No. AP2318
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    Cytochrome B5 Type A Human Recombinant 了解更多
  8. MRSA Antibody

    Catalog No. AP3016
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    MRSA (Staphylococcus aureus), Mouse Antibody 了解更多
  9. Procalcitonin Mouse

    Catalog No. AP3307
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    Procalcitonin Mouse Recombinant 了解更多
  10. TDP1 Human

    Catalog No. AP4016
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    Tyrosyl-DNA Phosphodiesterase 1 Human Recombinant 了解更多
  11. UBE2M Human

    Catalog No. AP5016
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    Ubiquitin Conjugating Enzyme E2M Human Recombinant 了解更多
  12. IL1RL1 Human, Sf9 Active

    Catalog No. AP5303
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    Interleukin-1 Receptor Like-1 Human Recombinant, Sf9 Active 了解更多
  13. IL 7 Mouse

    Catalog No. AP5360
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    Interleukin-7 Mouse Recombinant 了解更多
  14. IL1RL1 Human

    Catalog No. AP5432
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    Interleukin-1 receptor-like 1 Human Recombinant 了解更多
  15. IL1RL1 Human, Sf9

    Catalog No. AP5492
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    Interleukin-1 Receptor Like-1 Human Recombinant, Sf9 了解更多
  16. GCP-2 Human

    Catalog No. AP5744
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    Granulocyte Chemotactic Protein 2 (CXCL6) Human Recombinant 了解更多
  17. CD1B Human

    Catalog No. AP5779
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    CD1B Human Recombinant 了解更多
  18. HBsAg adw2

    Catalog No. AP6016
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    Hepatitis B Surface Antigen, adw2 Recombinant 了解更多
  19. Vadadustat

    Catalog No. A16794
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    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
  20. NS 1738

    Catalog No. A17079
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    α7 Positive Modulator
    NS 1738是α7阳性变构调节剂。在卵母细胞实验中,正调节 α7nAChR,EC50 为 3.4 μM。 了解更多
  21. LY2562175

    Catalog No. A17016
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    FXR 激动剂
    LY2562175是体外有效的选择性FXR激动剂,其EC50值为193 nM。具有强大的脂质调节特性,可降低临床前物种中的LDL和甘油三酸酯,同时提高HDL。 了解更多
  22. MIK665

    Catalog No. A18362
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    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
  23. Fosfomycin calcium

    Catalog No. A18154
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    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
  24. VU6005806

    Catalog No. A18488
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    M4 modulator
    VU6005806 (AZN-00016130) is a potent muscarnic acethylcholine receptor subtype 4 (M4) positive allosteric modulator (PAM), with EC50s of 94 nM, 28 nM, 87 nM and 68 nM for human, rat, dog and cyno M4, respectively. Used in the research of neuropsychiatric disorders. 了解更多
  25. Bepridil hydrochloride

    Catalog No. A18016
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    calcium channel blocker
    Bepridil hydrochloride (CERM 1978) is a calcium channel blocker, with antianginal activity. 了解更多
  26. ABBV-4083

    Catalog No. A20165
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    ABBV-4083 is an analog of Tylosin A that has potent anti-Wolbachia and anti-filarial activity. 了解更多
  27. NRA-0160

    Catalog No. A20128
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    Dopamine D4 receptor antagonist
    NRA-0160 is a selective dopamine D4 receptor antagonist, with a Ki value of 0.48 nM and with negligible affinity for dopamine D2 receptor (Ki: >10000 nM), D3 receptor (Ki: 39 nM), rat 5-HT2A receptor (Ki: 180 nM) and rat α1 adrenoceptor (Ki: 237 nM). 了解更多
  28. RV01

    Catalog No. A19104
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    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
  29. UPGL00004

    Catalog No. A19047
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    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
  30. cIAP1 Ligand-Linker Conjugates 15

    Catalog No. A19016
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    PROTAC linker
    cIAP1 Ligand-Linker Conjugates 15 incorporates an IAP ligand for the E3 ubiquitin ligase, and a PROTAC linker. cIAP1 Ligand-Linker Conjugates 15 can be used to design SNIPERs. 了解更多
  31. MV1

    Catalog No. A18963
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    IAP antagonist
    MV1 is an antagonist of IAP (inhibitor of apoptosis protein), leads to protein knockdown of HaloTag-fused proteins when combined with HaloTag ligand. 了解更多
  32. Bromodomain IN-1

    Catalog No. A18845
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    Bromodomain inhibitor
    Bromodomain IN-1 is a Bromodomain inhibitor extracted from patent WO2016069578A1, compound 4 . 了解更多
  33. UDM-001651

    Catalog No. A18843
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    PAR4 antagonist
    UDM-001651 is a potent , selective and orally active Protease-Activated Receptor 4 (PAR4) Antagonist with in Vivo Antithrombotic Efficacy (IC50 = 2.4 nM). 了解更多
  34. CB1 antagonist 2

    Catalog No. A18810
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    CB1 antagonist
    CB1 antagonist 2 is caimabinoid 1 (CB1) antagonist extracted from patent WO2016184310A1, compound 3, inhibits CB1 in vivo with an IC50 of 25.5 nM. 了解更多
  35. HPGDS inhibitor 2

    Catalog No. A18390
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    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
  36. NAMI-A

    Catalog No. A12143
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    ruthenium-based drug
    NAMI-A is a ruthenium-based drug characterised by the selective activity against tumour metastases, inhibits the adhesion and migration. 了解更多
  37. EC330

    Catalog No. A13799
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    leukemia inhibitory factor (LIF) inhibitor
    EC330 is a leukemia inhibitory factor (LIF) inhibitor. 了解更多
  38. T56-LIMKi

    Catalog No. A12266
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    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
  39. Glycolic acid oxidase inhibitor 1

    Catalog No. A13016
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    glycolate oxidase inhibitor
    Glycolic acid oxidase inhibitor 1 is a glycolate oxidase inhibitor, extracted from patent EP0021228A1, in Table IV. 了解更多
  40. CRA-026440

    Catalog No. A12179
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    HDAC inhibitor
    CRA-026440 is a potent, broad-spectrum HDAC inhibitor. 了解更多
  41. Cenerimod

    Catalog No. A20913
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    S1P1 agonist
    Cenerimod (ACT-334441) is a potent and orally available sphingosine 1-phosphate 1 receptor (S1P1) agonist extracted from patent WO 2016184939 A1 and WO 2011007324 A1, example 1, with an EC50 of 2.7 nM. 了解更多
  42. ENMD-119

    Catalog No. A20915
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    ENMD-119 is a 2-methoxyestradiol analogue with antiproliferative and antiangiogenic activity, and is suitable for inhibiting HIF-1α and STAT3 in human HCC cells. 了解更多
  43. MethADP sodium salt

    Catalog No. A21603
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    CD73 inhibitor
    MethADP (sodium salt) is a specific CD73 inhibitor. 了解更多
  44. ARN2966

    Catalog No. A21016
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    APP expression modulator
    ARN2966 is a potent post-transcriptional modulator of APP expression; reduces expression of APP with resultant lower production of Aβ. 了解更多
  45. Pparδ agonist 2

    Catalog No. A13262
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    PPARδ agonist
    Pparδ agonist 2 is a PPARδ agonist extracted from patent WO 2016057656 A1. 了解更多
  46. Nitroaspirin

    Catalog No. A19145
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    Nitroaspirin (NCX 4016) is a nitric oxide (NO) donor and a nitro-derivative of Aspirin, which combines with Nitroaspirin to inhibit cyclooxygenase. Nitroaspirin (NCX 4016) has antithrombotic and anti-platelet properties and acts as a direct and irreversible inhibitor of COX-1. 了解更多
  47. Ds-HAPP

    Catalog No. A19307
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    Ds-HAPP is an anthrancenyl and dansyl fluorophore ligand. 了解更多
  48. IDO-IN-11

    Catalog No. A19372
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    IDO inhibitor
    IDO-IN-11 is an indoleamine-2,3-dioxygenase (IDO) inhibitor with IC50s of 0.18 μM (Kinase) and 0.014 μM (Hela Cell), extracted from patent WO 2016041489 A1, compound 13. 了解更多
  49. IDO-IN-9

    Catalog No. A19647
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    IDO inhibitor
    IDO-IN-9 is an indoleamine-2,3-dioxygenase (IDO) inhibitor with IC50s of 0.011 μM (Kinase) and 0.0018 μM (Hela Cell), extracted from patent WO 2016041489 A1, compound 6. 了解更多
  50. CDK8-IN-3

    Catalog No. A19829
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    CDK8 inhibitor
    CDK8-IN-3 is an inhibitor of CDK8 extracted from patent WO2016041618A1, compound example 1.7. 了解更多

产品 51 到 100 共 123个

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