Other inhibitors

Items 901-950 of 980

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  1. KMO inhibitor

    UPF-648 is a potent kynurenine 3-monooxygenase (KMO) inhibitor; exhibits highly active at 1 uM (81 ?? 10% KMO inhibition); ineffective at blocking KAT activity.
  2. Camobucol is an orally active, phenolic antioxidant and anti-inflammatory compound with antirheumatic properties.
  3. photosynthetic electron transport inhibitor

    Amicarbazone(BAY-MKH3586; BAY314666) is a potent inhibitor of photosynthetic electron transport via binding to the Qb domain of photosystem II (PSII); herbicide with a broad spectrum of weed control.
  4. uricase inhibitor

    Potassium oxonate is an inhibitor of uricase, inhibits the phosphorylation of 5-FU to 5-fluorouridine-5'-monophosphate catalyzed by pyrimidine phosphoribosyl-transferase in a different manner from allopurinol in cell-free extracts and intact cells in vitro.
  5. Imexon (BM 06002) is an iminopyrrolidone aziridine with anti-cancer activity.
  6. Glyparamide is a chlorophenyl-containing sulfonylurea with hypoglycemic activity; Glyparamide rarely causes hepatic injury.
  7. TPT-260(TPU260) is a thiophene thiourea derivative with molecule weight 260.00 in free base form; There is no formal name yet, we temporally call this molecule as TPT-260.
  8. L,L-Dityrosine is a constituent of acid hydrolysates of a number of biological materials, including the insect cuticular resilin.
  9. L,L-Dityrosine (hydrochloride) is a constituent of acid hydrolysates of a number of biological materials, including the insect cuticular resilin.
  10. PIK3C3/Vps34 inhibitor

    SAR405 R enantiomer is the less active enantiomer of SAR405. SAR405 is a PIK3C3/Vps34 inhibitor.
  11. motilin receptor agonist

    Camicinal hydrochloride (GSK962040 hydrochloride) is a small molecule, selective motilin receptor agonist with pEC50 of 7.9.
  12. Gemcabene calcium (PD-72953 calcium), a first-in-class lipid-lowering agent, lowers low-density lipoprotein cholesterol (LDL-C), decreases triglycerides, and raises high-density lipoprotein cholesterol (HDL-C) and lowers pro-inflammatory acute-phase protein, C-reactive protein (CRP), exerting anti-inflammatory activity.
  13. VKOR antagonist

    Tecarfarin sodium (ATI-5923 sodium) is a novel orally active non-competitive vitamin K epoxide reductase (VKOR) antagonist, impairs the activation of the vitamin K-dependent clotting factors II, VII, IX and X.
  14. plant growth regulator

    Diethyl aminoethyl hexanoate citrate is a compound that is widely used as a plant growth regulator.
  15. Ecteinascidin-Analog-1 is a useful intermediate for chemical sythesis of Ecteinascidin analogues; Ecteinascidins is a family of tetrahydroisoquinoline alkaloids with wide range of antitumor and antimicrobial activities.
  16. Tenosal is a new compound obtained by esterifying salicylic acid with 2-thiophene-carboxylic acid and displays anti-inflammatory, analgesic and antipyretic properties.
  17. Heterotrimeric G-protein complex inhibitor

    PH-064 (BIM-46187) is an inhibitor of heterotrimeric G-protein complex.
  18. chymase inhibitor

    TY-51469 is a chymase inhibitor with IC50s for simian and human chymases of 0.4 and 7.0 nM, respectively.
  19. (Z)-MDL 105519 is the inactive isoform of MDL 105519.
  20. Methoxatin (disodium salt) as the cofactor in bovine plasma amine oxidase from resonance Raman spectroscopy.
  21. Glyoxalase I (GLO1) inhibitor

    Glyoxalase I inhibitor (free base) is a potent Glyoxalase I (GLO1) inhibitor, candidate for anticancer agents.
  22. squalene epoxidase inhibitor

    FR194738 is a squalene epoxidase inhibitor. FR194738 inhibits squalene epoxidase activity in HepG2 cell homogenates with an IC50 of 9.8 nM.
  23. motilin receptor agonist

    Camicinal (GSK962040) is a small molecule, selective motilin receptor agonist with pEC50 of 7.9.
  24. ELX-02 disulfate (NB-124 disulfate) is an investigational, advanced synthetic eukaryotic ribosome selective glycoside (ERSG). ELX-02 disulfate is being developed as a therapy for genetic diseases caused by nonsense mutations.
  25. ELX-02 sulfate (NB-124 sulfate) is an investigational, advanced synthetic eukaryotic ribosome selective glycoside (ERSG). ELX-02 sulfate is being developed as a therapy for genetic diseases caused by nonsense mutations.
  26. Imisopasem manganese , also known as M40403, or GC4419, is a manganese-based non-peptidyl mimetic of the human mitochondrial manganese superoxide dismutase (MnSOD), with potential antioxidant and chemo/radioprotective activities.
  27. Pimonidazole, also known as Ro 03-8799 and PD 126675, is a nitroimidazole drug with hypoxic selectivity and radiosensitizing property.
  28. triazole DAGL(α) inhibitor

    DO34 analog is a triazole DAGL(α) inhibitor extracted from patent WO2017096315 A1, compound 100.
  29. S107 hydrochloride is a RyR-selective 1,4-benzothiazepine derivative that stabilizes RyR2 channels by enhancing the binding affinity of calstabin2 to mutant and/or PKA-phosphorylated channels.
  30. anticholinergic antiparkinsonian agent

    Metixene hydrochloride is an anticholinergic antiparkinsonian agent, potently inhibits binding of quinuclidinyl benzilate (QNB) to the muscarinic receptor in rat brain cortical tissue, with an IC50 of 55 nM and a Kd of 15 nM.
  31. enkephalin degrading enzymes inhibitor

    Kelatorphan is a full inhibitor of enkephalin degrading enzymes.
  32. CDC7 kinase inhibitor

    (R)-Simurosertib ((R)-TAK-931) is the (R)-enantiomer of Simurosertib, Simurosertib (TAK-931) is a selective cycle 7 (CDC7) kinase inhibitor, with an IC50<0.3 nM.
  33. Amotosalen hydrochloride (S-59) is a light-activated, DNA-, RNA-crosslinking psoralen compound, which is used to neutralise pathogens.
  34. MBC-11 trisodium is a first-in-class conjugate of the bone-targeting bisphosphonate HEDP covalently linked to the antimetabolite Ara-C. Has potential to treat tumor-induced bone disease (TIBD).
  35. GJ103 sodium salt is an active analog of the read-through compound GJ072.
  36. MSI-1701 is an analogue of MSI-1436 which can control weight gain and blood glucose level extracted from patent US 7410959 B1.
  37. L-Homocysteine thiolactone hydrochloride is an intramolecular thioester of homocysteine; prevents translational incorporation of homocysteine into proteins.
  38. Oleanolic acid derivative 2 is an oleanolic acid derivative, which is a novel triterpenoid-steroid hybrid molecule.
  39. Oleanolic acid derivative 1 is an oleanolic acid derivative, which is a novel triterpenoid-steroid hybrid molecule.
  40. SAMDC inhibitor

    Sardomozide is an S-adenosylmethionine decarboxylase (SAMDC) inhibitor with an IC50 of 5 nM.
  41. CID797718 analog

    kb-NB77-78 is an analogue of CID797718, but shows no PKD inhibitory activity.
  42. VP40 Inhibitor

    ASN03576800 is an inhibitor of the VP40 matrix protein.
  43. β-cell protector

    RH01687 is a potent β-cell protector that exhibits β-cell-protective activities against endoplasmic reticulum (ER) stress.
  44. TAAR1 agonist

    RO5203648 hydrochloride is a partial agonist of Trace amine-associated receptor 1 (TAAR1).
  45. anti-infective agent

    RGW 611, a morpholine derivative, is an impurity of Nimorazole, which is an anti-infective agent against anaerobic bacteria and protozoa.
  46. antagonist of melanopsin-mediated phototransduction

    AA41612 is an antagonist of melanopsin-mediated phototransduction.
  47. Ces3 inhibitor

    WWL229 is a selective inhibitor of Ces3 that acts by inhibiting recombinant Ces3 and recapitulating the effects of WWL113 in adipocytes.
  48. polymerase inhibitor

    ERDRP-0519 is an orally available inhibitor of polymerase that shows efficacy against a lethal morbillivirus infection in a large animal model.
  49. non-narcotic analgesic

    Simetride, a non-narcotic analgesic, is an ingredient of Kyorin AP2 which is used to treat low back pain, symptomatic neuralgia, headache, menstrual pain and etc.
  50. antilipidemic agent

    Nicomol is a niacin derivative that exhibits antilipidemic activity.

Items 901-950 of 980

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