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Home >> Signaling Pathways >> Others >> Others

Others

Products for  Others

  1. Cat.No. Product Name Information
  2. GC35318 Amifampridine Amifampridine (3,4-Diaminopyridine) is an orally active, potent and cell permeable voltage-gated potassium (Kv) channel blocker (PCB). Amifampridine Chemical Structure
  3. GC15473 Amifostine cytoprotective adjuvant Amifostine Chemical Structure
  4. GC32021 Aminochlorthenoxazin (ICI 350) Aminochlorthenoxazin (ICI 350) is an antipyretic and analgesic agent. Aminochlorthenoxazin (ICI 350) Chemical Structure
  5. GC15727 Aminoguanidine hydrochloride iNOS inhibitor Aminoguanidine hydrochloride Chemical Structure
  6. GC35326 Amotosalen hydrochloride Amotosalen hydrochloride (S-59) is a light-activated, DNA-, RNA-crosslinking psoralen compound, which is used to neutralise pathogens. Amotosalen hydrochloride Chemical Structure
  7. GC13574 Amoxapine GLYT2a transport activity inhibitor Amoxapine Chemical Structure
  8. GC34470 AMXT-1501 tetrahydrochloride AMXT-1501 tetrahydrochloride is an orally active polyamine transport inhibitor. AMXT-1501 tetrahydrochloride Chemical Structure
  9. GC30122 AMZ30 AMZ30 is a selective, covalent inhibitors of protein phosphatase methylesterase-1(PME-1; IC50=600 nM); selectively inactivates PME-1 and reduces the demethylated form of PP2A in living cells. AMZ30 Chemical Structure
  10. GC33001 Anethole trithione Anethole trithione, a sulfur heterocyclic choleretic, is a bile secretion-stimulating agent. Anethole trithione Chemical Structure
  11. GC32467 Anisindione Anisindione is a synthetic anticoagulant, prevents the formation of active procoagulation factors II, VII, IX, and X. Anisindione Chemical Structure
  12. GC31859 Anitrazafen (LY 122512) Anitrazafen (LY 122512) is a topically effective antiinflammatory agent. Anitrazafen (LY 122512) Chemical Structure
  13. GC30846 Anle138b

    An inhibitor of protein aggregation

     Anle138b Chemical Structure
  14. GC35359 Anthraflavic acid Anthraflavic acid, a flavonoid, is a potent IQ mutagenicity inhibitor by virtue of its ability to inhibit both its microsomal and cytosolic activation pathways. Anthraflavic acid is a potent and specific cytochrome P-448 inhibitor activity an enzyme system closely associated with the activation of many chemical carcinogens. Anthraflavic acid Chemical Structure
  15. GC32656 Anti-Heart Failure Agent 1 Anti-Heart Failure Agent 1 an orally available compound suitable for the treatment of heart failure without inducing nausea, vomiting and restlessness. Anti-Heart Failure Agent 1 Chemical Structure
  16. GC33770 Anti-hypertensive sulfonanilide 1 Anti-hypertensive sulfonanilide 1 is a potent antihypertensive agent extracted from patent EP0338793A2, compound XVIIIa,b*, example No.1. Anti-hypertensive sulfonanilide 1 Chemical Structure
  17. GC31976 Anti-inflammatory agent 1 Anti-inflammatory agent 1 is an anti-inflammatory agent extracted from patent WO 2009003229 A1, example 36. Anti-inflammatory agent 1 Chemical Structure
  18. GC32009 Anti-inflammatory agent 2 Anti-inflammatory agent 2 (Compound 6) is a leukotriene synthesis (LTB4) inhibitor with an IC50 of 70 nM. Anti-inflammatory agent 2 Chemical Structure
  19. GC31244 Anti-neurodegeneration agent 1

    Anti-neurodegeneration agent 1 a neurodegeneration-targeting compound extracted from patent WO2008039514A1, Compound I.

     Anti-neurodegeneration agent 1 Chemical Structure
  20. GC10553 Anti-PIKFyve antibody against human PIKfyve Anti-PIKFyve Chemical Structure
  21. GC38146 Antiarol Antiarol (3,4,5-Trimethoxyphenol) is a natural compound isolated from Salmaliamalabaricum. Antiarol Chemical Structure
  22. GC31991 Antiasthmatic Compound 1

    Antiasthmatic Compound 1 is an antiasthmatic agent, which has the potential for allergic asthma treatment.

     Antiasthmatic Compound 1 Chemical Structure
  23. GC35360 Anticancer agent 3 Anticancer agent 3 (Compound 4) is a anti-cancer agent. Anticancer agent 3 Chemical Structure
  24. GC33745 Anticonvulsant agent 1 Anticonvulsant agent 1 is an anticonvulsant agent extracted from patent WO2001062726A2, Compound 156. Anticonvulsant agent 1 Chemical Structure
  25. GC16636 Antipyrine analgesic and antipyretic agent Antipyrine Chemical Structure
  26. GC35363 Antitumor Compound 1 Antitumor Compound 1 is a potent compound which comprises a new imidazopyridine having excellent antitumor activity as an active ingredient. Antitumor Compound 1 Chemical Structure
  27. GC33386 Antitumor Compound 2 Antitumor Compound 2, a butenylphenyl phosphate derivative, is a drug for mammary cancer and anovulatory sterility. Antitumor Compound 2 Chemical Structure
  28. GC33655 Antiulcer Agent 1 Antiulcer Agent 1 is a 2-(3,4-dimethoxyphenyl)ethylamine derivative for oral administration at an exploratory stage of new drug development. Antiulcer Agent 1 Chemical Structure
  29. GC35365 Apelin agonist 1 Apelin agonist 1 is an oral selective apelin agonist AM-2995, a agonist of the APJ (APLNR, angiotensin receptor like-1) receptor, may be used in the treatment of cardiovascular conditions. Apelin agonist 1 Chemical Structure
  30. GC16237 Apocynin Selective NADPH-oxidase inhibitor Apocynin Chemical Structure
  31. GC33737 Apronal (Allylisopropylacetylurea) A muscle relaxant Apronal (Allylisopropylacetylurea) Chemical Structure
  32. GC31850 Apyramide Apyramide is an?anti-inflammatory?agent (NSAID) and behaves as a prodrug of indomethacin. Apyramide Chemical Structure
  33. GC34423 AR-13324 M1 metabolite AR-13324 M1 metabolite is a hydrolysis metabolite of AR-13324 mesylate. AR-13324 M1 metabolite Chemical Structure
  34. GC35378 AR-9281 AR9281 (APAU) is a potent, selective and orally active soluble epoxide hydrolase (s-EH) inhibitor. AR-9281 Chemical Structure
  35. GC19435 Aramchol Aramchol, also known as arachidyl amido cholanoic acid, is a conjugate of arachidic acid and cholic acid . Aramchol Chemical Structure
  36. GC17225 ARL 67156 trisodium salt ARL67156 (FPL 67156) trisodium is a selective ecto-ATPase inhibitor. ARL 67156 trisodium salt Chemical Structure
  37. GC31913 ARN 077 (URB913) ARN 077 (URB913) is a potent and selective N-acylethanolamine acid amidase (NAAA) inhibitor with an IC50 of 7 nM for human NAAA. ARN 077 (URB913) Chemical Structure
  38. GC18448 ARN272 ARN272 is an anandamide transport inhibitor. ARN272 Chemical Structure
  39. GC32668 Arrhythmias-Targeting Compound 1 Arrhythmias-Targeting Compound 1 is used in the research of arrhythmias, extracted from patent WO 2001028992 A2. Arrhythmias-Targeting Compound 1 Chemical Structure
  40. GC32669 Arrhythmic-Targeting Compound 1 Arrhythmic-Targeting Compound 1 is used for the research of arrhythmic disease, with nitrogen-containing spirocycles. Arrhythmic-Targeting Compound 1 Chemical Structure
  41. GC10889 Artesunate Derivative of the natural product artemisinin Artesunate Chemical Structure
  42. GC13404 Articaine HCl Articaine HCl (Hoe-045) is an amide anaesthetic containing an ester group, reversibly binding to the α-subunit of the voltage-gated sodium channels within the inner cavity of the nerve, can provide effective pain relief. Articaine HCl Chemical Structure
  43. GC32936 ASP-9521 An inhibitor of 17β-HSD5/AKR1C3 ASP-9521 Chemical Structure
  44. GC30004 Asparagusic acid Asparagusic acid is a sulfur-containing flavor component produced by asparagus plants, with anti-parasitic effect. Asparagusic acid Chemical Structure
  45. GC12862 Aspartame non-saccharide sweetener Aspartame Chemical Structure
  46. GC35410 Aspartyl-alanyl-diketopiperazine Aspartyl-alanyl-diketopiperazine (DA-DKP) is an immunomodulatory molecule generated by cleavage and cyclization from the N-terminus of human albumin and can modulate the inflammatory immune response through a molecular pathway implicated in T- lymphocyte anergy. Aspartyl-alanyl-diketopiperazine Chemical Structure
  47. GC33886 Aspirin Aluminum (Aluminum diacetylsalicylate) Aspirin Aluminum (Aluminum diacetylsalicylate) is a novel intermolecular compound which can inhibit gastrointestinal mucosal disorders induced by NSAIDs (non-steroidal anti-inflammatory agents) extracted from patent WO 2010064441 A1. Aspirin Aluminum (Aluminum diacetylsalicylate) Chemical Structure
  48. GC32014 Asthma relating compound 1 Asthma relating compound 1 is an anti-asthmatic agent candidate extracted from patent EP0295656A1. Asthma relating compound 1 Chemical Structure
  49. GC32200 ATB107 ATB107 is a novel and potent inhibitor of indole-3-glycerol phosphate synthase (IGPS) with a KD of 3 μM. ATB107 Chemical Structure
  50. GC15770 Atglistatin ATGL inhibitor, potent and selective Atglistatin Chemical Structure
  51. GC35417 Athidathion Athidathion(GS-13006) is an organophosphate insecticide. Athidathion Chemical Structure
  52. GC18537 ATN-224 ATN-224 is a choline salt of tetrathiomolybdate and an inhibitor of superoxide dismutase 1 (SOD1; IC50s = 2.91 and 3.51 uM in human and mouse blood cells, respectively, in vitro). ATN-224 Chemical Structure
  53. GC10274 Atomoxetine HCl Atomoxetine HCl is a potent and selective noradrenalin re-uptake inhibitor (Ki values are 5, 77 and 1451 nM for inhibition of radioligand binding to human NET, SERT and DAT respectively). Atomoxetine HCl Chemical Structure
  54. GC34155 Atrimustine (Bestrabucil) Atrimustine (Bestrabucil) is a conjugate of chlorambucil and β-estradiol benzoate with the antitumor activity. Atrimustine (Bestrabucil) Chemical Structure
  55. GC34219 ATWLPPR Peptide TFA ATWLPPR Peptide TFA, a heptapeptide, acts as a selective neuropilin-1 inhibitor, inhibits VEGF165 binding to NRP-1, used in the research of angiogenesis. ATWLPPR Peptide TFA Chemical Structure
  56. GC31568 AU-224 AU-224 is a benzamide derivative used as a promising gastrointestinal prokinetic agent without significant side effects. AU-224 Chemical Structure
  57. GC35431 Aurothioglucose Aurothioglucose (Gold thioglucose) is a well known active-site inhibitor of TrxR1, inhibited TrxR1 activity in HeLa cell cytosol but had no effect on the viability of the cells. Aurothioglucose Chemical Structure
  58. GC30028 Auxinole Auxinole is a potent auxin antagonist of TIR1/AFB receptors, binding TIR1 to block the formation of the TIR1-IAA-Aux/IAA complex and so inhibits auxin-responsive gene expression. Auxinole Chemical Structure
  59. GC31627 AVE5688 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. AVE5688 Chemical Structure
  60. GC19045 AVN-944 AVN-944(VX-944) is a selective, noncompetitive inhibitor of the enzyme directed against human IMPDH with Ki of 6-10 nM for IMPDH1/IMPDH2. AVN-944 Chemical Structure
  61. GC14614 Avobenzone topical, broad range UV protector Avobenzone Chemical Structure
  62. GC30139 Avoralstat (BCX4161) Avoralstat (BCX4161) (BCX4161), a potent and orally active plasma kallikrein (PKK) inhibitor, is used for hereditary angioedema research. Avoralstat (BCX4161) Chemical Structure
  63. GC12429 AY 9944 dihydrochloride AY 9944 dihydrochloride is a specific cholesterol biosynthesis inhibitor. AY 9944 dihydrochloride Chemical Structure
  64. GC34479 AZ PFKFB3 26 AZ PFKFB3 26 is a potent and selective inhibitor of the metabolic kinase PFKFB3 with an IC50 of 23 nM. AZ PFKFB3 26 inhibits PFKFB1 and PFKFB2 with IC50s of 2.06 and 0.384 μM, respectively. AZ PFKFB3 26 Chemical Structure
  65. GC16119 Azacyclonol tranquilizer，antipsychotic Azacyclonol Chemical Structure
  66. GC14874 Azaserine tumor-inhibiting antibiotic Azaserine Chemical Structure
  67. GC31601 AZD 4017 AZD 4017 is a potent, selective 11β-Hydroxysteroid Dehydrogenase Type 1 (11β-HSD1) inhibitor, with an IC50 of 7 nM. AZD 4017 Chemical Structure
  68. GC35449 AZD8329 AZD8329 is a potent 11β-Hydroxysteroid dehydrogenase type 1 (11β-HSD1) inhibitor with an IC50 of 9 nM for human 11β-HSD1, displays excellent selectivity versus 11β-HSD2, 17β-HSD1 and 17β-HSD3. AZD8329 Chemical Structure
  69. GC30508 Azelaprag Azelaprag Chemical Structure
  70. GC34337 AzKTB AzKTB is a capture reagent which bears a short trypsin-cleavable peptide sequence between the azide module and the TAMRA/PEG-biotin labels. AzKTB Chemical Structure
  71. GC30634 Azobenzene Azobenzene can be used as an optical trigger for the design and synthesis of a large variety of photoresponsive systems. Azobenzene Chemical Structure
  72. GC14184 Azomycin antimicrobial antibiotic Azomycin Chemical Structure
  73. GC19445 Azoxymethane Azoxymethane, as a colon carcinogen, can lead to the formation of DNA adducts. Azoxymethane (AOM) causes O(6)-methylguanine adduct formation which leads to G-->A transitions. . Azoxymethane Chemical Structure
  74. GC19056 BAM 15

    BAM 15 is a novel mitochondrial protonophore uncoupler.

     BAM 15 Chemical Structure
  75. GC14668 BAMB-4 Inositol-1,4,5-trisphosphate-3-kinase A (ITPKA) inhibitor BAMB-4 Chemical Structure
  76. GC13517 BAPTA-AM

    BAPTA-AM is a well-known membrane-permeable Ca2+ chelator, to prevent cell injury by allaying the intracellular calcium overload

     BAPTA-AM Chemical Structure
  77. GC38351 Barbadin Barbadin is a novel and selective β-arrestin/β2-adaptin interaction inhibitor, has IC50 values of 19.1?μM for β-arrestin1 and 15.6?μM for β-arrestin2. Barbadin Chemical Structure
  78. GC32824 BAY-1816032 BAY-1816032 is a potent and oral available BUB1 (budding uninhibited by benzimidazoles 1) kinase inhibitor with an IC50 of 7 nM. BAY-1816032 Chemical Structure
  79. GC34164 BAY-320 BAY-320 is a Bub1 inhibitor, with an IC50 of 680 nM for human Bub1 in the presence of 2 mM ATP. BAY-320 Chemical Structure
  80. GC33236 BAY-524 BAY-524 is a potent Bub1 kinase inhibitor. BAY-524 inhibits the recombinant catalytic domain of human Bub1 with an IC50 of 450 nM. BAY-524 can be used for the research of anti-cancer in combination with other agents. BAY-524 Chemical Structure
  81. GC30619 BAY-677 BAY-677 is an inactive control for BAY-678. BAY-677 Chemical Structure
  82. GC31484 BAY-850 BAY-850 is a potent and isoform selective ATPase family AAA domain-containing protein 2 (ATAD2) inhibitor, with an IC50 of 166 nM. BAY-850 Chemical Structure
  83. GC19061 BAY-876 BAY-876 is the first highly selective GLUT1 inhibitor with IC50 of 0.002 uM. BAY-876 Chemical Structure
  84. GC33707 Beclamide (N-Benzyl-3-chloropropionamide) Beclamide (N-Benzyl-3-chloropropionamide) is a drug that possesses anticonvulsant activity, has been used as an anticonvulsant. Beclamide (N-Benzyl-3-chloropropionamide) Chemical Structure
  85. GC11228 Benazepril ACE inhibitor Benazepril Chemical Structure
  86. GC17941 Benazepril HCl Benazepril HCl, an angiotensin converting enzyme inhibitor, which is a medication used to treat high blood pressure. Benazepril HCl Chemical Structure
  87. GC31028 Bencianol (ZY15051) Bencianol (ZY15051) is a the semisynthetic flavinoid, with anti-spasmogenic activities. Bencianol (ZY15051) Chemical Structure
  88. GC30257 Bendazac L-Lysine Bendazac L-Lysine is one of agents that have been introduced for the management of cataracts, protecting the level of vision in patients, thus delaying the need for surgical intervention. Bendazac L-Lysine Chemical Structure
  89. GC35489 Benfluorex hydrochloride Benfluorex hydrochloride (JP-992 hydrochloride) is a hepatic nuclear factor 4 alpha (HNF4α) activator. Benfluorex hydrochloride Chemical Structure
  90. GC30747 Benfluralin Benfluralin is a kind of herbicide and an agrochemical which can be used as a pre-emergence herbicide used for the control of grass and other weeds in a range of food and non-food crops. Benfluralin Chemical Structure
  91. GC33174 Benin (Butocin) Benin (Butocin) is a potent cytostatic drug that can be used for the treatment of generalized carcinoma of the breast. Benin (Butocin) Chemical Structure
  92. GC35490 Benoxafos Benoxafos (HOE 2910) is an insecticide. Benoxafos Chemical Structure
  93. GC11886 Benserazide HCl Benserazide HCl (Serazide) is commonly used in Parkinson's disease and is an inhibitor of peripheral aromatic L-amino acid decarboxylase (AADC). Benserazide HCl Chemical Structure
  94. GC35491 Bentiromide Bentiromide is a peptide that is broken down in the pancreas by chymotrypsin. Bentiromide Chemical Structure
  95. GC32506 Benzcyclane (Bencyclane) Benzcyclane (Bencyclane) (Bencyclane; Benzcyclan) is a platelet aggregation inhibitor and a vasodilator effective in a variety of peripheral circulation disorders. Benzcyclane (Bencyclane) Chemical Structure
  96. GC38599 Benzobicyclon Benzobicyclon is a 4-HPPD inhibitor and herbicide that reacts with water to form a hydrolysate of the active herbicide benzobicycline, causing bleaching and death of weeds. Benzobicyclon Chemical Structure
  97. GC32624 Benzofurodil (Benfurodil) Benzofurodil (Benfurodil) is a cardiotonic, which is used for the chronic treatment of congestive heart failure. Benzofurodil (Benfurodil) Chemical Structure
  98. GC32497 Benzophenonetetracarboxylic acid (Benzophenone-3,3',4,4'-tetracarbonic acid) Benzophenonetetracarboxylic acid (Benzophenone-3,3',4,4'-tetracarbonic acid) (3,3',4,4'-Benzophenonetetracarboxylic acid (Benzophenone-3,3',4,4'-tetracarbonic acid)) is particularly useful in the preparation of high performance polyimides and also useful as curing agents for epoxy resins. Benzophenonetetracarboxylic acid (Benzophenone-3,3',4,4'-tetracarbonic acid) Chemical Structure
  99. GC32985 Benzo[a]pyrene (3,4-Benzopyrene) Benzo[a]pyrene (3,4-Benzopyrene) shows lung carcinogenicity in animal models, and it is frequently used in chemoprevention studies. Benzo[a]pyrene (3,4-Benzopyrene) Chemical Structure
  100. GC12697 Bephenium Hydroxynaphthoate Anthelmintic agent Bephenium Hydroxynaphthoate Chemical Structure
  101. GC38707 Beta-d-N4-hydroxycytidine Beta-d-N4-hydroxycytidine Chemical Structure

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