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  1. BoNTA LC inhibitor

    BoNT-IN-1 is a potent inhibitor of Botulinum neurotoxin A light chain (BoNTA LC) with IC50 of 0.9 uM.
  2. metal chelators

    HQ-415 is a class of clinically relevant bioactive metal chelators related to clioquinol. The effective concentration eliciting a EC50 for HQ-415 is 15 μM.
  3. SAHH inhibitor

    DZ2002 is a potent and reversible S-Adenosyl-L-homocysteine Hydrolase(SAHH; AdoHcy Hydrolase) inhibitor with Ki of 17.9 nM.
  4. α-glucoside hydrolase inhibitor

    Emiglitate (BAY o 1248) is a potent, selective and competitive inhibitor of α-glucoside hydrolase.
  5. E2F inhibitor

    HLM006474 is a pan E2F inhibitor, which inhibits E2F4 DNA-binding with an IC50 of 29.8 ?M in A375 cells.
  6. TrioN inhibitor

    ITX3 is a specific and nontoxic inhibitor of the TrioN (N-terminal GEF domain of the multidomain Trio protein) with IC50 of 76 uM; inhibits TrioN-stimulated RhoG exchange in vitro.
  7. insect chitinase and N- acetyl hexosaminidase inhibitor

    Chitinase-IN-2 is a insect chitinase and N- acetyl hexosaminidase inhibitor and pesticide; 50 μM/20 μM compound concentration's inhibitory percentage are 98%/92% for chitinase/N- acetyl-hexosaminidase respectively.
  8. insect chitinase and N- acetyl hexosaminidase inhibitor

    Chitinase-IN-1 is a insect chitinase and N- acetyl hexosaminidase inhibitor and pesticide; 50 uM/20 uM compound concentration's inhibitory percentage are 75%/67% for chitinase/N- acetyl-hexosaminidase respectively.
  9. PIP5K1α inhibitor

    ISA-2011B is a PIP5Kα inhibitor with promising anticancer effects .
  10. FPPS inhibitor

    NE 10790, a poor farnesyl pyrophosphate synthase inhibitor, is a phosphonocarboxylate analogue of the potent bisphosphonate risedronate and is a weak antiresorptive agent.
  11. (R)-Oxiracetam is the (R)-enantiomer of the nootropic drug oxiracetam. Oxiracetam (ISF 2522) is a nootropic drug of the racetam family and stimulant.
  12. Vitamin CK3 is the combination of Vitamin C and vitamin K3 (100:1 ratio) and has been shown to inhibit tumor growth and lung metastasis.
  13. RR6

    vanin inhibitor

    RR6 is a selective, reversible, and competitive vanin inhibitor.
  14. Furilazole(MON-13900) is a pesticide agent.
  15. Antitumor agent-3 is a potent compound which comprises a new imidazopyridine having excellent antitumor activity as an active ingredient.
  16. Chromafenozide (ANS118) is a lepidopteran insecticide; it is highly effective in controlling various lepidopteran pests.
  17. plant growth regulator

    Cloxyfonac is a plant growth regulator and a chemical transformation product; Pesticide agent.
  18. Benoxafos (HOE 2910) is an insecticide.
  19. Athidathion(GS-13006) is an organophosphate insecticide.
  20. Cobalt phthalocyanine is a catalyst of redox reaction, catalyzes aerobic regenerations of aldehydes and ketones from aldoximes and ketoximes has been developed.
  21. Novaluron is a chemical with pesticide properties, belonging to the class of insecticides called insect growth regulators.
  22. Ipfencarbazone is a substance being developed for the control of weeds such as watergrass in rice; herbicide agent.
  23. Ropidoxuridine (IPdR) is a novel orally available, halogenated thymidine analog and is a potential radiosensitizer for use in human tumors.
  24. RH1
    RH1 (NSC 697726) is a potent bioreductive agent with profound anti-cancer activity in vitro and in vivo.
  25. DβH inhibitor

    Etamicastat (BIA 5-453) is a potent and reversible peripheral dopamine-β-hydroxylase (DβH) inhibitor.
  26. P-selectin inhibitor

    PSI-697 is an oral P-selectin inhibitor with an IC50 of 125 μM.
  27. (R)-1,2,3,4-Tetrahydro-3-isoquinolinecarboxylic acid is a constrained Phe analogue which can fold into a beta-bend and a helical structure, and to adopt a preferred side-chain disposition in the peptide.
  28. HO inhibitor

    Tin(IV) mesoporphyrin IX dichloride (Stannsoporfin) is a heme oxygenase (HO) inhibitor being developed for the prevention of hyperbilirubinemia in infants at risk of developing jaundice, extracted from patent WO2011103196A1.
  29. S186 is a kind of sodium salts of calcium-acetylpropylamine phosphonate(APA); a new strontium-specific chelating agent.
  30. 20-Hydroxyeicosatetraenoic acid synthesis inhibitor

    TS-011 is a selective inhibitor of 20-Hydroxyeicosatetraenoic acid synthesis.
  31. CHAPS is a zwitterionic nondenaturing detergent for solubilizing membrane proteins.
  32. 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.
  33. Camobucol is an orally active, phenolic antioxidant and anti-inflammatory compound with antirheumatic properties.
  34. 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.
  35. 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.
  36. Imexon (BM 06002) is an iminopyrrolidone aziridine with anti-cancer activity.
  37. Glyparamide is a chlorophenyl-containing sulfonylurea with hypoglycemic activity; Glyparamide rarely causes hepatic injury.
  38. 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.
  39. L,L-Dityrosine is a constituent of acid hydrolysates of a number of biological materials, including the insect cuticular resilin.
  40. L,L-Dityrosine (hydrochloride) is a constituent of acid hydrolysates of a number of biological materials, including the insect cuticular resilin.
  41. PIK3C3/Vps34 inhibitor

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

    Camicinal hydrochloride (GSK962040 hydrochloride) is a small molecule, selective motilin receptor agonist with pEC50 of 7.9.
  43. 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.
  44. 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.
  45. plant growth regulator

    Diethyl aminoethyl hexanoate citrate is a compound that is widely used as a plant growth regulator.
  46. 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.
  47. Tenosal is a new compound obtained by esterifying salicylic acid with 2-thiophene-carboxylic acid and displays anti-inflammatory, analgesic and antipyretic properties.
  48. Heterotrimeric G-protein complex inhibitor

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

    TY-51469 is a chymase inhibitor with IC50s for simian and human chymases of 0.4 and 7.0 nM, respectively.
  50. (Z)-MDL 105519 is the inactive isoform of MDL 105519.

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