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  1. LH-RH, human is a biochem/physiol Actions LHRH Hypothalamic peptide that stimulates release of gonadotrophins from anterior pituitary, thus regulating reproductive functions.
  2. Anisole methoxybenzene is a colorless liquid with a smell reminiscent of anise seed, and in fact many of its derivatives are found in natural and artificial fragrances.
  3. DBU
    DBU is a chemical compound and belongs to the class of amidine compounds.
  4. Triisopropylsilane is a highly selective reducing agent which can be used to prepare anti-1,2-diols.
  5. Bisoctrizole is a broad-spectrum ultraviolet radiation absorber, absorbing UVB as well as UVA rays. Also a hybrid UV absorber, reflecting and scattering UV.
  6. PDX1 inducer

    BRD7552 is an inducer of transcription factor PDX1, which increases insulin expression.
  7. (Z)-2-decenoic acid is an unsaturated short chain fatty acid that is secreted by P. aeruginosa and induces a disp .
  8. 9-Dihydro-13-acetylbaccatin III (9-DHAB III) is an intermediate for taxol analog preparations.
  9. Benfotiamine is a synthetic S-acyl derivative of thiamine (vitamin B1), an antioxidant dietary supplement.
  10. BMX kinase inhibitor

    BMX-IN-1 is a highly selective and potent irreversible inhibitor which target the cysteine residue in the BMX ATP binding domain.
  11. COT/Tpl2 inhibitor

    Cot inhibitor-2 is a COT/Tpl2 inhibitor.
  12. Deferasirox Fe3+ chelate is a rationally-designed oral iron chelator; its main use is to reduce chronic iron overload in patients who are receiving long-term blood transfusions for conditions such as beta-thalassemia and other chronic anemias.
  13. EBE-A22 is a derivative of PD 153035 which can inhibit ErbB-1-phosphorylation, whereas EBE-A22 is inactive.
  14. Etimizol was shown to relieve amnesia effectively in the origin of which there is the hypoxic component (hypobaric hypoxia, actinomycin D, mechanical injury of the brain).
  15. GNG inhibitor

    MB05032 is a special and efficacious GNG inhibitor targeted the AMP binding site of fructose 1,6-bisphosphatase (FBPase) with an IC50 value of 16 nM.
  16. TK inhibitor

    N3PT is a potent and selective transketolase(TK) inhibitor (IC50= 22 nM for Apo-TK) both in vitro and in vivo.
  17. SE inhibitor

    NB-598 is a potent competitive inhibitor of squalene epoxidase (SE). NB-598 suppresses triglyceride biosynthesis through the farnesol pathway.
  18. Pafuramidine is an orally bioavailable prodrug of furamidine, which has clinical activity against Pneumocystis pneumonia.
  19. Pamabron is a common over-the-counter diuretic used for relief of menstrual-associated symptoms.
  20. Retinyl glucoside is a naturally occurring and biologically active metabolites of vitamin A, which are found in fish and mammals.
  21. sodium 4-pentynoate is a alkynylacetate analogue; can be metabolically incorporated onto cellular proteins through biosynthetic mechanisms for profiling of acetylated proteins in diverse cell types.
  22. Sodium formononetin-3'-sulfonate is a water-sol. derivate of formononetin.
  23. R18

    14.3.3 proteins Antagonist

    R18, antagonist of 14.3.3 proteins (KD ??? 80 nM). Competitively inhibits 14.3.3-ligand interactions without requiring phosphorylation.
  24. Immunomodulators

    Plumbagin, exhibits cytotoxicity in rodent models of carcinogenesis and carcinoma; has antifungal, antiviral, and antibacterial action.
  25. Morphine-like substance

    Beta-lipotropin (beta-LPH) was found to contain within its C-terminal sequence the primary structure of these peptides.
  26. Cell adhesion inhibitor

    K-7174 is a novel cell adhesion inhibitor; inhibits the expression of vascular cell adhesion molecule-1 (VCAM-1) induced by either IL-1beta or TNF-alpha.
  27. Cell adhesion inhibitor

    K-7174 dihydrochloride is a novel cell adhesion inhibitor; inhibits the expression of vascular cell adhesion molecule-1 (VCAM-1) induced by either IL-1beta or TNF-alpha.
  28. DNA repair inhibitor

    KRX-0402 is a small molecule that was specifically designed to block the DNA repair protein, MGMT. MGMT confers resistance to certain alkylating agents, such as temozolomide and BCNU, that are commonly used to treat brain cancer, melanoma and non-Hodgkin?€?s lymphoma.
  29. Finafloxacin hydrochloride is a fluoroquinolone compound.
  30. CBFBeta-SMMHC / RUNX1 inhibitor

    AI-10-49 is a protein-protein interaction inhibitor that selectively binds to CBFβ-SMMHC and disrupts its binding to RUNX1 with a FRET IC50 of 0.26 uM,
  31. Bucetin is an analgesic and antipyretice agent with a risk of carcinogenesis.
  32. AGE inhibitor

    LR-90 is an advanced glycation end product (AGE) inhibitor, inhibits inflammatory responses in human monocytes. LR-90 is also used in the research of diabetic animal model.
  33. RP 54275 (2-Octadecyl-1H-indole-5-carboxylic acid) is a novel hypocholesterolaemic drug.
  34. Ipenoxazone is a potent and centrally acting muscle relaxant.
  35. Docosahexaenoic Acid methyl ester is a methylated docosahexaenoic acid analog which can be intercalated into membrane phospholipids without being oxidized or hydrolyzed.
  36. Efaproxiral increases oxygen levels in hypoxic tumor tissues by binding non-covalently to the hemoglobin tetramer and decreasing hemoglobin-oxygen binding affinity.
  37. Visual cycle isomerase inhibitor

    Emixustat, a novel visual cycle modulator, is an inhibitor of the visual cycle isomerase with an IC50 value of 4.4 nM in vitro.
  38. nipradilol is an alpha(1),beta-blocker with a nitric oxide donative action
  39. Nalbuphine is a semi-synthetic opioid agonist-antagonist analgesic of the phenanthrene series
  40. LpxC inhibitor

    CHIR-090 is a potent, slow, tight-binding inhibitor of the LpxC deacetylase. It binds to E. coli LpxC with a Ki of 4.0 nM.
  41. Stiripentol is an epilepsy drug. It has been used as co-therapy for treatment of epilepsy
  42. Benperidol has been used in trials studying the treatment of Dementia, Depression, Schizophrenia, Anxiety Disorders, and Psychosomatic Disorders, among others.
  43. WF-11899A is a novel antifungal lipopeptide antibiotics were isolated from the culture broth of Coleophoma empetri F-11899
  44. Glycogen phosphorylase (GP) inhibitor

    AVE5688 is an inhibitor of glycogen phosphorylase (GP), with IC50s of 430 nM and 915 nM and Kds of 170 nM and 530 nM for rabbit muscle glycogen phosphorylase (rmGPb and rmGPa, respectively); AVE5688 can be used for the research of type 2 diabetes.
  45. antihypertensive agent

    RGH-5526 (GYKI-11679) is a new antihypertensive agent.
  46. UGT1A1 substrate

    UK-157147 is a substrate for UDP-glucuronosyltransferases (UGT1A1) with a Km value of 105 μM.
  47. Analeptic agent

    Mepixanox (Pimexone) is an analeptic drug used in respiratory and cardiorespiratory insufficiency.
  48. 20-HETE antagonist

    20-HEDE (WIT 002) is an antagonist of 20-hydroxyeicosatetraenoic acid (20-HETE).

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