Other inhibitors

Items 951-980 of 980

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  1. antilipidemic agent

    Nicomol is a niacin derivative that exhibits antilipidemic activity.
  2. p18INK inhibitor

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