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  1. AH10639 is a novel inhibitor of Pneumocystis carinii and Toxoplasma gondii dihydrofolate reductase.
  2. Beclamide is a chlorinated benzylpropanamide used as an anticonvulsant drug. It is used in the treatment of tonic-clonic seizyres and has sedative properties.
  3. NCGC00262650 is an inhibitor of AMA1-RON2 interaction and c-Src tyrosine kinase activity.
  4. 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).
  5. Nafocare B1 is a synthetic immune biological response modifier.
  6. NFTs tracer

    MK-6240 is a positron emission tomography (PET) tracer for neurofibrillary tangles (NFTs), exhibiting high specificity and selectivity for binding to NFTs.
  7. PET tracer

    T807 a novel tau positron emission tomography (PET) tracer.
  8. TN1

    HbF inducer

    TN1 is a potent fetal hemoglobin (HbF) inducer.
  9. Dansyl glutathione is a trapping agent for the quantitative estimation and identification of reactive metabolites.
  10. IGPS inhibitor

    ATB107 is a novel and potent inhibitor of indole-3-glycerol phosphate synthase (IGPS) with a KD of 3 μM.
  11. FOXM1 inhibitor

    RCM-1 is a FOXM1 inhibitor.
  12. breast cancer stem cells inhibitor

    ML239 is a potent and selective inhibitor of breast cancer stem cells, with an IC50 of 1.16 μM.
  13. nitrification inhibitor

    3-Methylpyrazole is used as a nitrification inhibitor of nitrification in soil.
  14. F 16915 is a docosahexaenoic acid derivative which can prevent heart failure-induced atrial fibrillation.
  15. p18 inhibitor

    NSC23005 sodium is a novel and effective p18 inhibitor (ED50=5.21 nM) in promoting Hematopoietic stem cells (HSCs) expansion in both murine and human models.
  16. BAL-30072, a siderophore sulfactam, is a monocyclic beta-lactam antibiotic, with activity against multiresistant gram-negative bacilli.
  17. PCA-1/ALKBH3 inhibitor

    HUHS015 is a potent PCA-1/ALKBH3 inhibitor both in vitro and in vivo.
  18. E-982 is extracted from the reference, compound 12.
  19. fibrinogen receptor antagonist

    SC-52012 is an orally active fibrinogen receptor antagonist, with antiplatelet activities.

  20. memory-enhancing agent

    CL-275838 is a memory-enhancing agent, also with potent antidepressant activities.
  21. PEP inhibitor

    Z-321 is a prolylendopeptidase (PEP) inhibitor.
  22. KW-6055 is a benzylpyridine derivative and has anti-amnesic activity.
  23. Trombodipine is an antithrombotic agent.
  24. hypolipidemic agent

    TA-1801 is a hypolipidemic agent.
  25. Fenclozine is a non-steroidal antiinflammatory drug extracted from patent WO 2012112690 A2.
  26. Valrocemide (TV1901) is a promising antiepileptic drug candidate that shows a broad spectrum of anticonvulsant activity.
  27. FKK

    bronchodilator

    FKK is an indazole derivative and also a novel bronchodilator.
  28. glycogen phosphorylase inhibitor

    Ingliforib is a glycogen phosphorylase inhibitor, with IC50s of 52, 352 and 150 nM for liver, muscle and brain glycogen phosphorylase, and has cardioprotective activity.
  29. Cease inhibitor

    SMP-028 is an inhibitor of neutral cholesterol esterase (CEase), with an IC50 of 1.01 μM.
  30. LS2265 is a taurine derivative of fenofibrate and can induce proliferation of peroxisomes in liver cells of rats.
  31. impurity of Calcitriol

    Calcitriol Impurities D is the impurity of Calcitriol, Calcitriol is the hormonally active form of vitamin D, Calcitriol is the active metabolite of vitamin D3 that activates the vitamin D receptor (VDR).
  32. hTGase inhibitor

    LDN-27219 is a potent inhibitor of hTGase(Tissue transglutaminase) with an IC50 of 0.6 uM.
  33. squalene synthase inhibitor

    Lapaquistat acetate (TAK-475) is a squalene synthase inhibitor, blocking the conversion of farnesyl diphosphate (FPP) to squalene.
  34. HbS polymerization inhibitor

    Voxelotor (GBT 440) is an orally bioavailable sickle hemoglobin (HbS) polymerization inhibitor.
  35. α-Tocopherol phosphate is the compound demonstrating the highest vitamin E activity, which is available both in its natural form as RRR-alpha-tocopherol isolated from plant sources.
  36. Glufosfamide is a novel alkylating agent in which the active metabolite of isophosphoramide mustard is glycosidically linked to β-D-glucose.
  37. PROTO-1 shows significant protection of hair cells, with HC50(concentration that would produce 50% hair cell survival) of 1 μM-10 μM (1 μM??HC50??10 μM).
  38. BoNTA LC inhibitor

    BoNT-IN-1 is a potent inhibitor of Botulinum neurotoxin A light chain (BoNTA LC) with IC50 of 0.9 uM.
  39. 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.
  40. SAHH inhibitor

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

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

    HLM006474 is a pan E2F inhibitor, which inhibits E2F4 DNA-binding with an IC50 of 29.8 ?M in A375 cells.
  43. 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.
  44. 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.
  45. 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.
  46. PIP5K1α inhibitor

    ISA-2011B is a PIP5Kα inhibitor with promising anticancer effects .
  47. 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.
  48. (R)-Oxiracetam is the (R)-enantiomer of the nootropic drug oxiracetam. Oxiracetam (ISF 2522) is a nootropic drug of the racetam family and stimulant.
  49. 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.
  50. RR6

    vanin inhibitor

    RR6 is a selective, reversible, and competitive vanin inhibitor.

Items 901-950 of 13505

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