Other inhibitors

Items 951-980 of 980

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  1. p18INK inhibitor

    NSC23005 is a p18INK inhibitor. NSC23005 potently promotes hematopoietic stem cell (HSC) expansion (ED50 = 5.21 nM).
  2. Thiambutosine was a candidate for treatment of lepromatous leprosy.
  3. Isocyclosporin A is a rearranged degradation product formed by acid treatment of cyclosporin A under aqueous and non-aqueous conditions.
  4. Dextromethorphan (Discontinued) (DXM or DM) is an antitussive (cough suppressant) drug of the morphinan class with sedative and dissociative properties.
  5. 3CLpro inhibitor

    GC376 is a 3CLpro inhibitor (3C-like protease inhibitor).
  6. inhibitor for GA perception

    TSPC is an inhibitor for GA perception by in vitro and in planta evaluations.
  7. autoinducer of P. fischeri luciferase

    N-(beta-ketocaproyl)-L-Homoserine lactone (N-(Ketocaproyl)-L-homoserine lactone, N-(β-Ketocaproyl)-L-hoMoserine lactone) is an autoinducer of P. fischeri luciferase and a component of quorum regulatory sensing.
  8. Eph family tyrosine kinase inhibitor

    Ehp inhibitor 2 is a Eph family tyrosine kinase inhibitor.
  9. S-adenosylhomocysteine hydrolase inhibitor

    3-Deazaadenosine (hydrochloride) is an inhibitor of S-adenosylhomocysteine hydrolase, with a Ki of 3.9 ?M; 3-Deazaadenosine has anti-inflammatory, anti-proliferative and anti-HIV activity.
  10. antiproliferative agent

    Coumarin-3-carboxylic acid (2- Oxochromene-3-carboxylic acid) is an important initial compound for the synthesis of coumarins which are well known natural products for their diverse biological activities. Lanthanide complexes of Coumarin-3-carboxylic acid exhibit antiproliferative activity towards K-562 cell line.
  11. inhibitor of glycogen synthase kinase 3

    5-bromoindole is an important pharmaceutical chemical intermediate and a potential inhibitor of glycogen synthase kinase 3 (GSK-3).
  12. non-steroidal anti-inflammatory drug

    Indoprofen is a non-steroidal anti-inflammatory drug, provide insight into treatments for spinal muscular atrophies.
  13. AKR1C3 inhibitor

    Stylopine is a potent AKR1C3 inhibitor.
  14. Violanthrone-79 is an n-channel organic semiconductor
  15. AH10639 is a novel inhibitor of Pneumocystis carinii and Toxoplasma gondii dihydrofolate reductase.
  16. Beclamide is a chlorinated benzylpropanamide used as an anticonvulsant drug. It is used in the treatment of tonic-clonic seizyres and has sedative properties.
  17. NCGC00262650 is an inhibitor of AMA1-RON2 interaction and c-Src tyrosine kinase activity.
  18. PLAP inhibitor

    ML-095 is an inhibitor of PLAP (IC50 = 3.7 μM) that demonstrates high selectivity against the related alkaline phosphatases, TNAP and IAP (IC50s > 100 μM).
  19. FTO inhibitor

    FB23 is a potent and selective inhibitor of N6-methyladenosine (m6A) demethylase FTO (fat mass and obesity associated protein).
  20. hypoglycemic agent

    Carbutamide (BZ-55) is an orally active and first-generation sulfonylurea with hypoglycemic activity.
  21. Methyl 13-cis-4-Oxoretinoate is a bioactive chemical.
  22. transcriptional inhibitor of G0/G1 switch 2

    NS-3-008 hydrochloride is an orally active transcriptional inhibitor of G0/G1 switch 2 (G0s2) with an IC50 of 2.25 μM. NS-3-008 hydrochloride can be used for chronic kidney disease.
  23. U 19963 (1,3-Bis(4-fluorophenyl)thiourea) is a bioactive compound.
  24. NSC 191412 (1-(4-Fluorophenyl)-3-phenylthiourea) is an active compound.
  25. Adipamidoxime (NSC 70868) is a new bioactive compoud.
  26. oxyhaemoglobin stabilizer

    Velaresol, also known as BW12C or BW12C79, is a oxyhaemoglobin stabilizer.
  27. anticonvulsant/antiepileptic agent

    Lvguidingan (Anticonvulsant 7903, 3,4-dichlorophenyl propenylisobutylamide) is an anticonvulsant/antiepileptic agent. Lvguidingan (Anticonvulsant 7903) is found to be able to increase the concentration of 5-HT and 5-HIAA in mice brain.
  28. Tri-Salicylic Acid (Trisalicylic Acid), a product of the thermal decomposition of aspirin, is a biochemical for proteomics research.
  29. chemical cyclophilin A inhibitor

    TMN355 is a potent chemical cyclophilin A inhibitor and reduces foam cell formation and cytokine secretion. TMN355 is used for atherosclerosis.
  30. liver receptor homolog 1 (LRH-1; NR5A2) inverse agonist

    ML-180 (SR1848) is a potent orphan nuclear receptor liver receptor homolog 1 (LRH-1; NR5A2) inverse agonist with an IC50 of 3.7 ?M.

Items 951-980 of 980

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