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产品 301 到 350 共 1548个

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  1. Broflanilide

    Catalog No. A19824
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    Broflanilide is a potential insecticide and metabolized to desmethyl-broflanilide, which is a potent antagonist at the insect resistant-to-dieldrin (RDL) GABA receptor, and inhibits S. litura RDL GABAR, with an IC50 value of 1.3 nM. 了解更多
  2. Fluxametamide

    Catalog No. A19815
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    Fluxametamide is an insecticide with wide spectrum, acts as an antagonist of GABA- and glutamate-gated chloride channels, with IC50 of 1.95 nM and 225 nM for M. domestica GABACls and GluCls. 了解更多
  3. SPP-86

    Catalog No. A19812
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    RET inhibitor
    SPP-86 is a potent and selective cell permeable inhibitor of RET tyrosine kinase, with an IC50 of 8 nM. 了解更多
  4. BCECF-AM

    Catalog No. A19809
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    intracellular pH fluorescent indicator
    BCECF-AM is a cell membrane permeable compound, widely used as a fluorescent indicator for intracellular pH. 了解更多
  5. O-304

    Catalog No. A19807
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    AMPK activator
    O-304 is a first-in-class, orally available pan-AMPK activator, which increases AMPK activity by suppressing the dephosphorylation of pAMPK. 了解更多
  6. Zuranolone

    Catalog No. A19805
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    GABAA receptor agonist
    Zuranolone is a potent GABAA receptor agonist with EC50s of 296 and 163 nM for α1β2γ2 and α4β3δ GABAA receptors, respectively. 了解更多
  7. D-Lin-MC3-DMA

    Catalog No. A19797
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    siRNA delivery vehicle
    D-Lin-MC3-DMA, an ionizable cationic lipid, is a potent siRNA delivery vehicle. 了解更多
  8. CMPD101

    Catalog No. A19795
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    GRK2/GRK3 inhibitor
    CMPD101, is a novel membrane-permeable, small-molecule inhibitor of both GRK2 and GRK3 with IC50s of 18 nM and 5.4 nM. CMPD101 also inhibits ROCK-2 and PKCα (IC50s=1.4 μM and 8.1 μM, respectively). 了解更多
  9. ATRA-hydroxyimino

    Catalog No. A19791
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    ATRA-hydroxyimino (CRABP-II ligand 1), the Retinoic acid (ATRA)-based moiety, binds to cIAP1 ligand (Bestatin) via a linker to form SNIPER to degrade CRABP-II in IMR-32 cells. 了解更多
  10. 5-BrUTP sodium salt

    Catalog No. A19789
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    5-BrUTP sodium salt can be used to label RNA to measure the transcription. 了解更多
  11. PROTAC CRABP-II Degrader-1

    Catalog No. A19782
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    CRABP-II degrader
    PROTAC CRABP-II Degrader-1 is a potent cellular retinoic acid binding protein (CRABP-II) degrader based on cIAp1. 了解更多
  12. Calcein Blue

    Catalog No. A19780
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    blue-fluorescent dye
    Calcein Blue is a short-term, blue-fluorescent dye for labeling live cells. 了解更多
  13. GSK3004774

    Catalog No. A19779
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    CaSR agonist
    GSK3004774 is a potent, nonabsorbable agonist of CaSR, with an pEC50 of 7.3, 6.6 and 6.5 for human, mouse and rat CaSR, respectively. GSK3004774 shows an EC50 of 50 nM for human CaSR. 了解更多
  14. ACP-105

    Catalog No. A19778
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    androgen receptor modulator
    ACP-105 is an orally available, selective amd potent androgen receptor modulator (SARM), with pEC50s of 9.0 and 9.3 for AR wild type and T877A mutant, respectively. 了解更多
  15. Retagliptin Phosphate

    Catalog No. A19777
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    DPP-4 inhibitor
    Retagliptin Phosphate is pharmaceutical composition of DPP-4 inhibitor for treating type-2 diabetes. 了解更多
  16. PROTAC CRABP-II Degrader-2

    Catalog No. A19773
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    CRABP-II degrader
    PROTAC CRABP-II Degrader-2 is a potent cellular retinoic acid binding protein (CRABP-II) degrader based on cIAp1. 了解更多
  17. PROTAC CRABP-II Degrader-3

    Catalog No. A19764
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    CRABP-II degrader
    PROTAC CRABP-II Degrader-3 is a potent cellular retinoic acid binding protein (CRABP-II) degrader based on cIAp1. 了解更多
  18. Dabsyl chloride

    Catalog No. A19755
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    amine derivatizing agent
    Dabsyl chloride is an amine derivatizing agent, able to give rise to stable products that can be easily monitored spectrophotometrically at 460 nm; Dabsyl chloride also used for labeling amino acids. 了解更多
  19. Foliglurax

    Catalog No. A19753
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    mGluR4 modulator
    Foliglurax (PXT002331) is a highly selective and potent, brain-penetrant metabotropic glutamate receptor 4 positive allosteric modulator (mGluR4 PAM) with an EC50 of 79 nM. Antiparkinsonian effect. 了解更多
  20. GDC-0927

    Catalog No. A19747
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    estrogen receptor antagonist
    GDC-0927 (SRN-927) is a novel, potent, non-steroidal, orally bioavailable, selective estrogen receptor antagonist. 了解更多
  21. CT-721

    Catalog No. A19742
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    Bcr-Abl kinase inhibitor
    CT-721 is a potent and time-dependent Bcr-Abl kinase inhibitor with an IC50 of 21.3 nM for wild-type Bcr-Abl kinase, and possesses anti-chronic myeloid leukemia (CML) activities. 了解更多
  22. INCB-057643

    Catalog No. A19737
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    BET inhibitor
    INCB-057643 is a novel, orally bioavailable BET inhibitor. 了解更多
  23. 4-Octyl Itaconate

    Catalog No. A19731
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    4-Octyl Itaconate is a cell-permeable Itaconate derivative. Itaconate is an anti-inflammatory metabolite that activates Nrf2 via alkylation of KEAP1. 了解更多
  24. Seclidemstat

    Catalog No. A19730
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    LSD1 inhibitor
    Seclidemstat (SP-2577) is a potent and orally bioavailable LSD1 inhibitor, with a mean IC50 of 127 nM. 了解更多
  25. LSZ-102

    Catalog No. A19728
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    estrogen receptor degrader
    LSZ-102 is a potent, orally bioavailable selective estrogen receptor degrader with an IC50 of 0.2 nM. 了解更多
  26. KDM2A/7A-IN-1

    Catalog No. A19724
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    KDM2A/7A inhibitor
    KDM2A/7A-IN-1 is a first-in-class, selective and cell-permeable inhibitor of histone lysine demethylases KDM2A/7A, with an IC50 of 0.16?μM for KDM2A, exhibits 75 fold selevtivity over other JmjC lysine demethylases, and is inactive on methyl transferases, and histone acetyl transferases. 了解更多
  27. Desisobutyryl-ciclesonide

    Catalog No. A19718
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    Desisobutyryl-ciclesonide is the active metabolite of Ciclesonide. Desisobutyryl-ciclesonide has affinity for the glucocorticoid receptor. 了解更多
  28. PAT-505

    Catalog No. A19715
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    autotaxin inhibitor
    PAT-505 is a potent, selective, noncompetitive and orally available autotaxin inhibitor, with an IC50 of 2 nM in Hep3B cells, 9.7 nM in human blood and 62 nM in mouse plasma. 了解更多
  29. E7046

    Catalog No. A19711
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    EP4 antagonist
    E7046 is an orally bioavailable and specific EP4 antagonist, with IC50 of 13.5 nM and Ki of 23.14 nM, exhibiting anti-tumor activities. 了解更多
  30. 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
  31. VU0650786

    Catalog No. A19689
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    CNS penetrant modulator
    VU0650786 is a potent and selective CNS penetrant negative allosteric modulator of metabotropic glutamate receptor subtype 3 (mGlu3 NAM), with an IC50 of 392 nM. VU0650786 has antidepressant and anxiolytic activity in rodents. 了解更多
  32. GPR120 Agonist 1

    Catalog No. A19679
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    GPR120 agonist
    GPR120 Agonist 1 is a potent and selective GPR120 agonist, and possesses promising antidiabetic effect and good safety profile to be a development candidate. 了解更多
  33. Imatinib carbaldehyde

    Catalog No. A19670
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    Imatinib carbaldehyde (CGP-57148B carbaldehyde), the Imatinib (ABL inhibitor) based moiety, binds to IAP ligand via a linker to form SNIPER. 了解更多
  34. 4-Hydroxychalcone

    Catalog No. A19662
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    4-Hydroxychalcone is a chalcone metabolite with anti-angiogenic and anti-inflammatory activities. 了解更多
  35. Bestatin-amido-Me

    Catalog No. A19661
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    Bestatin-amido-Me, the Bestatin-based IAP ligand, binds to ABL inhibitor via a linker to form SNIPER. 了解更多
  36. NCT-506

    Catalog No. A19660
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    ALDH1A1 inhibitors
    NCT-506 is an orally bioavailable aldehyde dehydrogenase 1A1 (ALDH1A1) inhibitors with an IC50 of 7 nM. 了解更多
  37. Asciminib

    Catalog No. A19658
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    Bcr-Abl inhibitor
    Asciminib (ABL001) is a potent and selective allosteric Bcr-Abl inhibitor; inhibits Ba/F3 cells grown with an IC50 of 0.25 nM. 了解更多
  38. GNF5-amido-Me

    Catalog No. A19651
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    GNF5-amido-Me, the GNF5 (ABL inhibitor) based moiety, binds to IAP ligand via a linker to form SNIPER. 了解更多
  39. NAcM-OPT

    Catalog No. A19646
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    DCN1 inhibitor
    NAcM-OPT is an orally bioavailable cullin neddylation 1 (DCN1) inhibitor, which potently inhibits the DCN1-UBE2M interaction. 了解更多
  40. MV-1-NH-Me

    Catalog No. A19642
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    MV-1-NH-Me, the MV-1 based IAP ligand, binds to ABL inhibitor via a linker to form SNIPER. 了解更多
  41. CRS400393

    Catalog No. A19640
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    CRS400393 is a potent antimycobacterial agent, with MIC of 0.03, 2, and ?? 0.12 ?g/mL against M. abs., M. avium, M. intracellulare, and M. tuberculosis, respectively. 了解更多
  42. Melinamide

    Catalog No. A19631
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    cholesterol absorption inhibitor
    Melinamide, an amide derivative of an unsaturated long-chain fatty acid, is an inhibitor of cholesterol absorption with an IC50 of 20.9 μM. 了解更多
  43. Dasatinib carbaldehyde

    Catalog No. A19627
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    Dasatinib carbaldehyde (BMS-354825 carbaldehyde), the Dasatinib (ABL inhibitor) based moiety, binds to IAP ligand via a linker to form SNIPER . 了解更多
  44. ABT-702 dihydrochloride

    Catalog No. A19624
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    AK inhibitor
    ABT-702 dihydrochloride is a potent adenosine kinase (AK) inhibitor (IC50=1.7 nM). 了解更多
  45. Modecainide

    Catalog No. A19620
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    Modecainide is a major metabolite of Encainide, which is an antiarrhythmic agent. 了解更多
  46. SNIPER(ABL)-058

    Catalog No. A19616
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    SNIPER(ABL)-058, conjugating Imatinib (ABL inhibitor) to LCL161 derivative (IAP ligand) with a linker, induces the reduction of BCR-ABL protein with a DC50 of 10 μM. 了解更多
  47. TAK-828F

    Catalog No. A19611
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    RORγt inverse agonist
    TAK-828F is a potent, selective, and orally available retinoic acid receptor-related orphan receptor γt (RORγt) inverse agonist (binding IC50=1.9 nM, reporter gene IC50=6.1 nM). 了解更多
  48. Heparan Sulfate

    Catalog No. A19609
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    Heparan sulfate, a complex and linear polysaccharide, exists as part of glycoproteins named heparan sulfate proteoglycans, which are expressed abundantly on the cell surface and in the extracellular matrix. 了解更多
  49. SNIPER(ABL)-024

    Catalog No. A19607
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    SNIPER(ABL)-024, conjugating GNF5 (ABL inhibitor) to LCL161 derivative (IAP ligand) with a linker, induces the reduction of BCR-ABL protein with a DC50 of 5μM. 了解更多
  50. PI3Kγ inhibitor 2

    Catalog No. A19606
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    PI3Kγ inhibitor
    PI3Kγ inhibitor 2 (Compound 16) is an orally bioavailable, CNS-penetrant, isoform selective PI3Kγ inhibitor with a Ki of 4 nM. 了解更多

产品 301 到 350 共 1548个

每页
页面:
  1. 5
  2. 6
  3. 7
  4. 8
  5. 9

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