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  1. Cat.No. Product Name Information
  2. GC38904 Desoxycorticosterone pivalate Desoxycorticosterone pivalate (DOCP) is a mineralocorticoid hormone and an analog of Desoxycorticosterone. Desoxycorticosterone pivalate Chemical Structure
  3. GC31869 Dexamethasone 9,11-epoxide Dexamethasone 9,11-epoxide, a compound extracted from patent CN 106520896 A and RU 2532902 C1, is an intermediate in the preparation of dexamethasone. Dexamethasone 9,11-epoxide Chemical Structure
  4. GC10655 Dexrazoxane cardioprotective agent Dexrazoxane Chemical Structure
  5. GC38241 Dextran Dextran (Dextran 40) has an inhibitory effect on thrombocyte aggregation and coagulation factors and is used as a plasma volume expander. Dextran Chemical Structure
  6. GC17252 Dextrose (D-glucose) Dextrose (D-glucose) (Glucose), a monosaccharide, is an important carbohydrate in biology. Dextrose (D-glucose) Chemical Structure
  7. GC38769 DFP00173 DFP00173 is a potent and selective aquaporin-3 (AQP3) inhibitor. DFP00173 Chemical Structure
  8. GC30335 Diatrizoic acid (Amidotrizoic acid) Diatrizoic acid (Amidotrizoic acid) (Diatrizoate) is an iodinated radiocontrast agent and has the potential for radiographic imaging of the airways. Diatrizoic acid (Amidotrizoic acid) Chemical Structure
  9. GC16674 Dibenzothiophene Intermediate of organic synthesis Dibenzothiophene Chemical Structure
  10. GC38770 Dichlorophenyl-ABA Dichlorophenyl-ABA is an inhibitor of transthyretin (TTR) amyloid fibril formation, inhibiting aggregate formation in more than 80% in TTR L55P-expressing cells. Dichlorophenyl-ABA Chemical Structure
  11. GC33569 Dicloralurea (DCU) Dicloralurea (DCU) is a veterinary food additive that inhibits methane production in herbicide ruminants, acts as a growth stimulant. Dicloralurea (DCU) Chemical Structure
  12. GC14336 Dicyclomine HCl Dicyclomine HCl is a potent and orally active muscarinic cholinergic receptors antagonist. Dicyclomine HCl Chemical Structure
  13. GC30606 Diethyl aminoethyl hexanoate citrate (DA-6 citrate) Diethyl aminoethyl hexanoate citrate (DA-6 citrate) is a compound that is widely used as a plant growth regulator. Diethyl aminoethyl hexanoate citrate (DA-6 citrate) Chemical Structure
  14. GC30163 Diethyl phosphate (Diethyl phosphoric acid) Diethylphosphate (DEP) is product of metabolism and of environmental degradation of a commonly used insecticide Chlorpyrifos. Diethyl phosphate (Diethyl phosphoric acid) Chemical Structure
  15. GC38771 Diethyl succinate Diethyl succinate (Diethyl Butanedioate) is used at physiological pH and crosses biological membranes, incorporates into cells in tissue culture and is metabolized by the TCA cycle. Diethyl succinate Chemical Structure
  16. GC32949 Diethyl-pythiDC Diethyl-pythiDC is an inhibitor of collagen prolyl 4-hydroxylases (CP4Hs). Diethyl-pythiDC Chemical Structure
  17. GC30590 Diethylamino hydroxybenzoyl hexyl benzoate (DHHB) Diethylamino hydroxybenzoyl hexyl benzoate (DHHB) is a photostable UV-A absorber. Diethylamino hydroxybenzoyl hexyl benzoate (DHHB) Chemical Structure
  18. GC11776 Diethylmaleate Maleic acid diethyl ester Diethylmaleate Chemical Structure
  19. GC16213 Difloxacin HCl Difloxacin HCl is a broad-spectrum antibacterial drug. Difloxacin HCl Chemical Structure
  20. GC31895 Diflumidone (R807) Diflumidone (R807) is a non-steroidal antiinflammatory drug. Diflumidone (R807) Chemical Structure
  21. GC13358 Difluprednate Corticosteroid Difluprednate Chemical Structure
  22. GC16682 Difopein 14.3.3 protein inhibitor Difopein Chemical Structure
  23. GC15863 Dilazep dihydrochloride vasodilator that acts as an adenosine reuptake inhibitor Dilazep dihydrochloride Chemical Structure
  24. GC34557 DIM-C-pPhCO2Me DIM-C-pPhCO2Me is a nuclear receptor 4A1 (NR4A1) antagonist. Antineoplastic activity. DIM-C-pPhCO2Me Chemical Structure
  25. GC32884 DIM-C-pPhOCH3 A Nur77 receptor agonist DIM-C-pPhOCH3 Chemical Structure
  26. GC16262 Dimesna Uroprotective agent Dimesna Chemical Structure
  27. GC31182 Dimetacrine (Dimethacrine) Dimetacrine (Dimethacrine) is a useful antidepressant effect, and can be used for the research of various types of depression. Dimetacrine (Dimethacrine) Chemical Structure
  28. GC30221 Dimethyl 4-hydroxyisophthalate Dimethyl 4-hydroxyisophthalate is a methyl salicylate analogue. Dimethyl 4-hydroxyisophthalate Chemical Structure
  29. GC40997 Dimethyl biphenyl-4,4'-dicarboxylate Dimethyl biphenyl-4,4'-dicarboxylate is a planar biphenyldicarboxylic acid ester used as a hepatoprotectant in the treatment of chronic hepatitis. Dimethyl biphenyl-4,4'-dicarboxylate Chemical Structure
  30. GC33535 Dioxybenzone (Benzophenone-8) Dioxybenzone (Benzophenone-8) is an organic compound used in sunscreen to block UVB and short-wave UVA (ultraviolet) rays. Dioxybenzone (Benzophenone-8) Chemical Structure
  31. GC17794 Diperodon HCl Diperodon is a local anaesthetics, by the action of hydrolazes in blood serum is decomposed. Diperodon HCl Chemical Structure
  32. GC14984 Diphenylpyraline HCl Diphenylpyraline HCl is a potent histamine H1receptor antagonist. Diphenylpyraline HCl Chemical Structure
  33. GC35868 DIPQUO DIPQUO is an activator of the bone marker alkaline phosphatase (ALP), with an EC50 of 6.27 μM in C2C12 cells. DIPQUO Chemical Structure
  34. GC31982 Dipyrocetyl Dipyrocetyl is an anti-inflammatory and analgesic agent extracted from patent WO 2011132171 A1. Dipyrocetyl Chemical Structure
  35. GC31454 Dirlotapide (CP742033) Dirlotapide (CP742033) (CP742033) is a gut-selective inhibitor of microsomal triglyceride transfer protein (MTP) that reliably produces weight loss in obese dogs. Dirlotapide (CP742033) Chemical Structure
  36. GC35871 Diroximel fumarate Diroximel fumarate (ALKS 8700) is an orally-active and well-tolerated monomethyl fumarate (MMF) prodrug in a controlled-release formulation. Diroximel fumarate Chemical Structure
  37. GC10981 Disodium (R)-2-Hydroxyglutarate Disodium (R)-2-Hydroxyglutarate (Disodium (R)-2-hydroxyglutarate) is the principal metabolite accumulating in neurometabolic disease D-2-hydroxyglutaric aciduria. Disodium (R)-2-Hydroxyglutarate Chemical Structure
  38. GC31286 Dixyrazine Dixyrazine, a phenothiazine derivative, can prevent brain oedema induced by intracarotid injection of protamine sulphate. Dixyrazine Chemical Structure
  39. GC35872 DiZPK DiZPK is a structural analog of pyrrolysine (Pyl), acting as a photocrosslinker for identifying direct protein-protein interactions in living prokaryotic and eukaryotic cells. DiZPK Chemical Structure
  40. GC19125 DiZPK Hydrochloride DiZPK Hydrochloride as a probe has two characteristics, the first DiZPK Hydrochloride as a derivative of pyrrolysine can be used for genetic codon expansion technology DiZPK Hydrochloride Chemical Structure
  41. GC33498 DL-3-Indolylglycine DL-3-Indolylglycine is an unnatural amino acid that is very similar to Tryptophan, with the indole moiety directly attached to the α-position. DL-3-Indolylglycine Chemical Structure
  42. GC35875 DL-alpha-Tocopherol methoxypolyethylene glycol succinate DL-alpha-Tocopherol methoxypolyethylene glycol succinate solution (TPGS-750-M) is an amphiphile, acts as a surfactant. DL-alpha-Tocopherol methoxypolyethylene glycol succinate Chemical Structure
  43. GC30369 DL-Carnitine ((±)-Carnitin) DL-Carnitine ((±)-Carnitin) is a racemic mixture of L-Carnitine and D-Carnitine, regulates fatty acid transport in mitochondria, elevates serum carnitine fractions. DL-Carnitine ((±)-Carnitin) Chemical Structure
  44. GC30236 DL-Lysine ((±)-2,6-Diaminocaproic acid) DL-Lysine ((±)-2,6-Diaminocaproic acid) is a racemic mixture of the D-Lysine and L-Lysine. DL-Lysine ((±)-2,6-Diaminocaproic acid) Chemical Structure
  45. GC35880 DL-threo-2-methylisocitrate DL-threo-2-methylisocitrate is a substrate of isocitrate lyase 1(ICL1). DL-threo-2-methylisocitrate Chemical Structure
  46. GC16274 DL-threo-2-methylisocitrate sodium

    Substrate of isocitrate lyase 1(ICL1)

     DL-threo-2-methylisocitrate sodium Chemical Structure
  47. GC12595 DL-α-Difluoromethylornithine (hydrochloride hydrate) DL-α-Difluoromethylornithine (hydrochloride hydrate) (DFMO hydrochloride hydrate) is a specific, irreversible inhibitor of the enzyme ornithine decarboxylase. DL-α-Difluoromethylornithine (hydrochloride hydrate) is a medication for the treatment of African trypanosomiasis and excessive facial hair growth in women. DL-α-Difluoromethylornithine (hydrochloride hydrate) Chemical Structure
  48. GC35878 DLin-KC2-DMA An ionizable amino lipid DLin-KC2-DMA Chemical Structure
  49. GC33476 DLinDMA DLinDMA is a key lipid component of stable nucleic acid lipid particles as a benchmark. DLinDMA Chemical Structure
  50. GC31030 DMP 696 DMP 696 is a selective corticotropin-releasing hormone receptor 1 (CRHR1) antagonist, used for the treatment of anxiety and depression. DMP 696 Chemical Structure
  51. GC35885 DMT1 blocker 1 DMT1 blocker 1 is a blocker of divalent metal transporter 1 (DMT1) with an IC50 of 0.64 μM, is expected to block iron uptake by enterocytes in vivo. DMT1 blocker 1 Chemical Structure
  52. GC35886 DMT1 blocker 2 DMT1 blocker 2 is a direct inhibitor of divalent metal transporter 1 (DMT1), with an IC50 of 0.83 μM. DMT1 blocker 2 Chemical Structure
  53. GC38207 DNA2 inhibitor C5 DNA2 inhibitor C5 is a potent, competitive and specific inhibitor of DNA2 nuclease activity with an IC50 of 20 μM. DNA2 inhibitor C5 inhibits nuclease, DNA dependent ATPase, helicase, and DNA binding activities of DNA2. DNA2 inhibitor C5 is a promising lead compound to develop sensitizers for cancer chemotherapeutics that cause replication stress. DNA2 inhibitor C5 Chemical Structure
  54. GC31446 DO34 DO34 is a highly potent, selective and centrally active diacylglycerol lipase (DAGL) inhibitor, with an IC50 of 6 nM for DAGLα conversion of SAG to 2-AG, and an IC50 for DAGLβ. DO34 Chemical Structure
  55. GC31496 DO34 analog DO34 analog is a triazole DAGL(α) inhibitor extracted from patent WO2017096315 A1, compound 100. DO34 analog Chemical Structure
  56. GC30357 DO3A tert-Butyl ester (DO3A tert-butyl) DOTA tert-Butyl ester is a benxyl derivative of the cyclic tosamide; can be nitrated directly; is more convenient to incorporate the nitro group after deprotection lithium aluminum hydride. DO3A tert-Butyl ester (DO3A tert-butyl) Chemical Structure
  57. GC30461 Dobupride Dobupride is a novel gastroprokinetic drug. Dobupride Chemical Structure
  58. GC12881 Docosanol (Abreua) Docosanol (Abreua) is a saturated fatty alcohol used traditionally as an emollient, emulsifier, and thickener in cosmetics, and nutritional supplement; inhibitor of lipid-enveloped viruses including herpes simplex. Docosanol (Abreua) Chemical Structure
  59. GC30687 Dolutegravir intermediate-1 Dolutegravir intermediate-1 is a synthetic intermediate of Dolutegravir extracted from patent WO 2016125192 A2. Dolutegravir intermediate-1 Chemical Structure
  60. GC38553 Dooku1 Dooku1, an analog of Yoda1, is a selective antagonist of the endogenous Piezo1 channel. Dooku1 Chemical Structure
  61. GC13932 Dorzolamide Carbonic anhydrase inhibitor Dorzolamide Chemical Structure
  62. GC30481 DOTA derivative DOTA derivative is a benxyl derivative of the cyclic tosamide; can be nitrated directly; is more convenient to incorporate the nitro group after deprotection lithium aluminum hydride. DOTA derivative Chemical Structure
  63. GC35895 Dotinurad Dotinurad is a potent and selective urate reabsorption inhibitor. Dotinurad Chemical Structure
  64. GC13976 Doxapram HCl Potassium channel inhibitor Doxapram HCl Chemical Structure
  65. GC38384 DPA-714 DPA-714 is a high affinity translocator protein (TSPO) ligand (Ki=7 nM), which is designed with a fluorine atom in its structure, allowing labelling with fluorine -18 and in vivo imaging using positron emission tomography. DPA-714 Chemical Structure
  66. GC35899 Draflazine Draflazine (R-75231) is a ENT1 inhibitor. Draflazine Chemical Structure
  67. GC32635 Drobuline hydrochloride Drobuline hydrochloride is an anti-arrhythmic agent with cardiac depressant. Drobuline hydrochloride Chemical Structure
  68. GC14609 Dropropizine Racemic non-opiate antitussive agent Dropropizine Chemical Structure
  69. GC32525 Droxicainide Droxicainide is an antiarrhythmic agent. Droxicainide Chemical Structure
  70. GC32492 DS-1040 Tosylate DS-1040 Tosylate is an orally active, selective inhibitor of activated thrombin-activatable fibrinolysis inhibitor (TAFIa) with IC50s of 5.92 nM and 8.01 nM for human and rat TAFIa. DS-1040 Tosylate Chemical Structure
  71. GC30540 Ds-HAPP Ds-HAPP is an anthrancenyl and dansyl fluorophore ligand. Ds-HAPP Chemical Structure
  72. GC38906 DS18561882 DS18561882 is a highly potent, isozyme-selective methylenetetrahydrofolate dehydrogenase 2 (MTHFD2) inhibitor with an IC50 value of 0.0063 μM. DS18561882 also has inhibitory effect on MTHFD1 (IC50=0.57 μM). DS18561882 exhibits a good oral pharmacokinetic profile. DS18561882 Chemical Structure
  73. GC35901 DS21360717 DS21360717 is a potent and orally active FER tyrosine kinase inhibitor, with an IC50 of 0.49 nM. Anti-cancer activity. DS21360717 Chemical Structure
  74. GC35902 DS28120313 DS28120313 (compound 32) is an orally hepcidin production inhibitor with an IC50 of 0.093 μM. DS28120313 Chemical Structure
  75. GC12042 DSP-4 DSP-4 is a highly and selective adrenergic neurotoxin. DSP-4 Chemical Structure
  76. GC34433 DTPA-DAB2 DAB2-DTPA is a conjugate of DTPA with two DAB used in the photooxidation experiments. DTPA-DAB2 Chemical Structure
  77. GC32647 DU717 DU-717 is an antihypertensive agent. DU717 Chemical Structure
  78. GC31031 Duoperone Duoperone is a neuroleptic agent and also a antiemetic agent in animal models. Duoperone Chemical Structure
  79. GC33083 DUPA(OtBu)-OH DUPA(OtBu)-OH is a DUPA precursor. DUPA is used as the targeting moiety to actively deliver Docetaxel (DTX) for treatment of Prostate-Specific Membrane Antigen (PSMA) expressing prostate cancer. DUPA(OtBu)-OH Chemical Structure
  80. GC35920 DZ2002 DZ2002 is an orally active, reversible and low-cytotoxic type III SAHH inhibitor (Ki=17.9 nM), with good immunosuppressive activity. DZ2002 Chemical Structure
  81. GC30470 E-982 E-982 is a steroid used for the on-line screening of the DNA unwinding element binding protein (DUE-B) immobilized protein column. E-982 Chemical Structure
  82. GC34103 E260

    E260 is a Fer/FerT kinase inhibitor.

     E260 Chemical Structure
  83. GC35959 EBE-A22 EBE-A22 is a derivative of PD 153035 which can inhibit ErbB-1-phosphorylation, whereas EBE-A22 is inactive. EBE-A22 Chemical Structure
  84. GC11676 EC 23 retinoic acid receptors agonist EC 23 Chemical Structure
  85. GC34017 EC-17 disodium salt EC-17 (disodium salt) is a folate receptor alpha (FRα) targeting contrast agent with fluorescent properties in the visible light spectrum. The peak excitation and emission wavelengths of EC-17 are 470/520?nm. EC-17 disodium salt Chemical Structure
  86. GC32756 EC330 EC330 is a leukemia inhibitory factor (LIF) inhibitor. EC330 Chemical Structure
  87. GC34161 Ecteinascidin-Analog-1 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. Ecteinascidin-Analog-1 Chemical Structure
  88. GC12838 Edaravone A radical scavenger and antioxidant Edaravone Chemical Structure
  89. GC32909 EED inhibitor-1 EED inhibitor-1 is an embryonic ectoderm development (EED) inhibitor extracted from patent US20160176882 A1, compound example 2. EED inhibitor-1 exhibits IC50s of 59, 89, 26 nM in EED Alphascreen binding, LC-MS and ELISA assay. EED inhibitor-1 Chemical Structure
  90. GC33348 EF-5 EF-5 (EF5; 2-Nitroimidazole) is a hypoxia labeling agent used to identify hypoxia in cells. EF-5 Chemical Structure
  91. GC30283 Eflornithine (DFMO) Eflornithine (DFMO) is a specific, irreversible inhibitor of the enzyme ornithine decarboxylase. Eflornithine (DFMO) Chemical Structure
  92. GC30308 Eflornithine hydrochloride (DFMO hydrochloride) Eflornithine hydrochloride (DFMO hydrochloride) is a specific, irreversible inhibitor of the enzyme ornithine decarboxylase. Eflornithine hydrochloride (DFMO hydrochloride) Chemical Structure
  93. GC32581 Efloxate (Angorlisin) Efloxate (Angorlisin) is a vasodilator, used to treat chronic coronary insufficiency and Angina pectoris, Efloxate (Angorlisin) Chemical Structure
  94. GC16183 EG00229

    Nrp1 inhibitor

     EG00229 Chemical Structure
  95. GC33272 EG01377 EG01377 is a potent, bioavailable and selective inhibitor of neuropilin-1 (NRP1), with a Kd of 1.32 μM, and IC50s of both 609 nM for NRP1-a1 and NRP1-b1. EG01377 has antiangiogenic, antimigratory, and antitumor effects. EG01377 Chemical Structure
  96. GC40813 Eicosapentaenoic Acid ethyl ester Fish oils in the diet have anti-inflammatory and cardiovascular benefits due to an abundance of ω-3 polyunsaturated fatty acids (PUFAs), including eicosapentaenoic acid (EPA). Eicosapentaenoic Acid ethyl ester Chemical Structure
  97. GC34182 Elacytarabine (CP 4055) Elacytarabine (CP 4055) (CP 4055) is a lipid-conjugated derivative of the nucleoside analog cytarabine. Elacytarabine (CP 4055) (CP 4055) is an antineoplastic drug with cytotoxicity in solid tumors. Elacytarabine (CP 4055) Chemical Structure
  98. GC35972 Eldecalcitol-d6 Eldecalcitol-d6 is the deuterium labeled Eldecalcitol. Eldecalcitol-d6 Chemical Structure
  99. GC19392 Eliglustat Eliglustat is an specific, potent and orally active glucocerebroside synthase inhibitor with an IC50 of 24 nM. Eliglustat Chemical Structure
  100. GC43595 Eliglustat (hemitartrate) Eliglustat is a potent and selective inhibitor of glucosylceramide synthase with an IC50 value of 40 nM for the reduction of glucosylceramide synthesis in K562 cells. Eliglustat (hemitartrate) Chemical Structure
  101. GC30936 ELN484228 ELN484228 is a blocker of α-synuclein which is a key protein in Parkinson’s disease. ELN484228 Chemical Structure

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