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Home >> Signaling Pathways >> Others >> Others

Others

Products for  Others

  1. Cat.No. Product Name Information
  2. GC10582 Betacarotene Betacarotene (Provitamin A), a carotenoid compound, is a naturally-occurring vitamin A precursor. Betacarotene Chemical Structure
  3. GC33890 Betamethasone 17-benzoate Betamethasone 17-benzoate is a representative steroid, which can be used in the treatment of recurrent aphothous ulcers (RAU). Betamethasone 17-benzoate Chemical Structure
  4. GC12122 Betamethasone Dipropionate Glucocorticoid receptor agonist Betamethasone Dipropionate Chemical Structure
  5. GC13638 Betamethasone Valerate anti-inflammatory corticosteroid Betamethasone Valerate Chemical Structure
  6. GC33906 Betamethasone-17-butyrate-21-propionate Betamethasone-17-butyrate-21-propionate is a topical corticosteroid with potential in the treatment of inflammatory skin diseases. Betamethasone-17-butyrate-21-propionate Chemical Structure
  7. GC30492 BFCAs-1 BFCAs-1 is a polyamino polycarboxylic bifunctional chelating agent(BFCAs); a broad range of applications in chemistry, biology and medicine and diagnostic imaging (MRI, SPECT, PET). BFCAs-1 Chemical Structure
  8. GC32178 BI-3802 BI-3802 is a highly potent BCL6 degrader and inhibits the Bric-à-brac (BTB) domain of BCL6 with an IC50 of ≤3 nM. BI-3802 induces the polymerization of BCL6 and promotes BCL6 degration depended on E3 ligase SIAH1. BI-3802 has antitumor activity. BI-3802 Chemical Structure
  9. GC32990 BI-3812 BI-3812 is potent and efficacious BCL6 inhibitor, inhibiting the BTB domain of BCL6, with an IC50 of ≤3 nM; BI-3812 has antitumor activity. BI-3812 Chemical Structure
  10. GC35514 BI-4916 BI-4916 is a prodrug of BI-4924. BI-4924 is a NADH/NAD+-competitive PHGDH inhibitor. BI-4916 Chemical Structure
  11. GC35515 BI-4924 BI-4924 is a lipophilic, highly plasma protein bound selective phosphoglycerate dehydrogenase (PHGDH) inhibitor (IC50=3 nM) with excellent microsomal, as well as hepatocytic stability. Intracellular trapping of BI-4924 disrupts serine biosynthesis with an IC50 of 2200 nM at 72 h. BI-4924 Chemical Structure
  12. GC14267 Bialaphos (sodium salt)

    natural non-selective phytotoxin

     Bialaphos (sodium salt) Chemical Structure
  13. GC42929 BIBB 515 2,3-Oxidosqualene cyclase (OSC) is an important enzyme in the biosynthesis of animal, plant, and fungal sterols. BIBB 515 Chemical Structure
  14. GC31417 BIBR 1087 SE (Desethyl Dabigatran Etexilate) BIBR 1087 SE (Desethyl Dabigatran Etexilate) is an intermediate metabolite of dabigatran etexilate. BIBR 1087 SE (Desethyl Dabigatran Etexilate) Chemical Structure
  15. GC34050 Bidisomide (SC40230) Bidisomide (SC40230) (SC40230) is a class I antiarrhythmic agent. Bidisomide (SC40230) Chemical Structure
  16. GC33908 Bimosiamose (TBC 1269) Bimosiamose (TBC 1269) (TBC-1269) is a nonoligosaccharide pan-selectin antagonist with IC50s of 88 μM, 20 μM, and 86 μM for E-selectin, P-selectin, and L-selectin, respectively. Bimosiamose (TBC 1269) Chemical Structure
  17. GC14990 Biocytin Versatile marker used in anterograde, retrograde and intracellular neuroanatomical investigations and in biotinidase assays. Biocytin Chemical Structure
  18. GC13376 Biotin-tyramide Biotin-tyramide is a biotin derivative used for tyramide signal amplification (TSA), as a reagent to amplify both immunohistochemical signals and in situ hybridization protocols. Biotin-tyramide Chemical Structure
  19. GC11364 Bisacodyl stimulant laxative drug Bisacodyl Chemical Structure
  20. GC17707 Bismuth Subsalicylate Prostaglandin G/H Synthase 1/2 inhibitor Bismuth Subsalicylate Chemical Structure
  21. GC30483 Bisoctrizole Bisoctrizole is a broad-spectrum ultraviolet radiation absorber, absorbing UVB as well as UVA rays; also reflects and scatters UV. Bisoctrizole Chemical Structure
  22. GC31480 BM-131246 BM-131246 is an oral antidiabetic agent. BM-131246 Chemical Structure
  23. GC31534 BM152054 BM152054 can promote glucose utilization in peripheral tissues by enhancing insulin action. BM152054 Chemical Structure
  24. GC35540 Boc-MLF TFA Boc-MLF (TFA) is a peptide, used as a specific formyl peptide receptor (FPR) antagonist, also inhibits the signaling through formyl peptide receptor like 1 (FPRL1) at higher concentrations. Boc-MLF TFA Chemical Structure
  25. GC31061 BoNT-IN-1 BoNT-IN-1 is a potent inhibitor of Botulinum neurotoxin A light chain (BoNTA LC) with IC50 of 0.9 uM. BoNT-IN-1 Chemical Structure
  26. GC34502 BPK-29 BPK-29 is a specific ligand that disrupts the atypical orphan nuclear receptor NR0B1-protein (such RBM45 and SNW1) interactions by covalently modifying C274. BPK-29 impairs the anchorage-independent growth of KEAP1-mutant cancer cells. BPK-29 Chemical Structure
  27. GC38643 BPK-29 hydrochloride BPK-29 hydrochloride is a specific ligand that disrupts the atypical orphan nuclear receptor NR0B1-protein (such RBM45 and SNW1) interactions by covalently modifying C274. BPK-29 hydrochloride impairs the anchorage-independent growth of KEAP1-mutant cancer cells. BPK-29 hydrochloride Chemical Structure
  28. GC13958 BPTES A GLS inhibitor BPTES Chemical Structure
  29. GC10233 BRD 7552 PDX1 inducer BRD 7552 Chemical Structure
  30. GC10259 BRD4770 novel G9a(EHMT2) inhibitor BRD4770 Chemical Structure
  31. GC12811 BRD7116 inhibitor of leukemia stem cell activity BRD7116 Chemical Structure
  32. GC38743 Bredinin aglycone Bredinin aglycone (5-Hydroxy-1H-imidazole-4-carboxamide) is a purine nucleotide analogue. Bredinin aglycone Chemical Structure
  33. GC30874 Bretylium tosylate A class III antiarrhythmic agent Bretylium tosylate Chemical Structure
  34. GC34891 BRM/BRG1 ATP Inhibitor-1 BRM/BRG1 ATP Inhibitor-1 (compound 14) is an orally active allosteric dual brahma homolog (BRM)/SWI/SNF related matrix associated actin dependent regulator of chromatin subfamily A member 2 (SMARCA2) and brahma related gene 1 (BRG1)/SMARCA4 ATPase activity inhibitor, both IC50s are below 0.005 ?M. BRM/BRG1 ATP Inhibitor-1 has anticancer activity. BRM/BRG1 ATP Inhibitor-1 Chemical Structure
  35. GC16979 Bromethalin rodenticide Bromethalin Chemical Structure
  36. GC35556 Bromfenac sodium hydrate Bromfenac sodium hydrate (Bromfenac monosodium salt sesquihydrate) is a potent and orally active inhibitor of COX, with IC50s of 5.56 and 7.45 nM for COX-1 and COX-2, respectively. Bromfenac sodium hydrate Chemical Structure
  37. GC32577 Bromindione (Fluidane) Bromindione (Fluidane) is a potent, long-acting, inandione-derived, oral anticoagulant compound. Bromindione (Fluidane) Chemical Structure
  38. GC33694 Bromisoval (Bromovalerylurea) Bromisoval (Bromovalerylurea) has anti-inflammatory effects. Bromisoval (Bromovalerylurea) Chemical Structure
  39. GC30666 Bronchospasmolytic agent 1 Bronchospasmolytic agent 1, a synthetic flutropium bromide compound, acts as a bronchospasmolytic agent. Bronchospasmolytic agent 1 Chemical Structure
  40. GC39165 BTL-105 BTL-105 is a monobiotinylated Phos-tag derivative for the detection of phosphopeptides and phosphoproteins. BTL-105 Chemical Structure
  41. GC30061 BTTAA

    BTTAA is a Cu(I)-stabilizing ligand, whch performs potently with ubiquitin Glu18AzF.

     BTTAA Chemical Structure
  42. GC18127 BTZ043 Racemate DprE1 inhibitor BTZ043 Racemate Chemical Structure
  43. GC11141 BTZO 1 migration inhibitory factor (MIF) binder BTZO 1 Chemical Structure
  44. GC30364 Bucetin (3-Hydroxy-p-butyrophenetidide) Bucetin (3-Hydroxy-p-butyrophenetidide) (3-Hydroxy-p-butyrophenetidide) is an analgesic and antipyretic compound. Bucetin (3-Hydroxy-p-butyrophenetidide) Chemical Structure
  45. GC33875 Bucloxic acid (804CB) Bucloxic acid (804CB) is an anti-inflammatory pyrrazole derivative. Bucloxic acid (804CB) Chemical Structure
  46. GC16118 Buflomedil HCl Buflomedil HCl is a vasodilator used to treat claudication or the symptoms of peripheral arterial disease. Buflomedil HCl Chemical Structure
  47. GC32661 Bunaftide (Bunaftine) Bunaftide (Bunaftine) (Bunaftine; Bunaphtide; Meregon) is an antiarrhythmic agent. Bunaftide (Bunaftine) Chemical Structure
  48. GC30487 Bupropion morpholinol D6 (Hydroxy Bupropion D6) Bupropion morpholinol D6 (Hydroxy Bupropion D6) Chemical Structure
  49. GC33725 Butacaine Butacaine is a reversible nerve conduction blocker. Butacaine Chemical Structure
  50. GC15738 BVT 2733 BVT 2733 is a novel, small-molecule, nonsteroidal, isoform-selective inhibitor of 11beta-hydroxysteroid dehydrogenase type 1 (11β-HSD1) with IC50 of 96 nM (mice). BVT 2733 Chemical Structure
  51. GC31368 BVT-14225

    BVT-14225 is a selective 11β-Hydroxysteroid dehydrogenase type 1 (11β-HSD1) inhibitor with an IC50 of 52 nM.

     BVT-14225 Chemical Structure
  52. GC13643 c-di-AMP

    C-di-AMP is a STING agonist, which binds to the transmembrane protein STING, thereby activating the TBK3-IRF3 signaling pathway, subsequently triggering the production of type I IFN and TNF.

     c-di-AMP Chemical Structure
  53. GC33095 C-Phycocyanin (C-PC) C-phycocyanin (C-PC) is a protein pigment which is also widely used as an excellent nutrient supplement for human beings. C-Phycocyanin (C-PC) Chemical Structure
  54. GC35576 CADD522 CADD522 is a RUNX2-DNA binding inhibitor (downregulates RUNX2-mediated transcription of downstream target genes), with an IC50 of 10 nM. CADD522 inhibits primary tumor growth and experimental metastasis of tumor cells in the lungs of immune-compromised mice. CADD522 can be used in study of cancer. CADD522 Chemical Structure
  55. GC11242 Calcium Gluceptate Calcium Gluceptate is an endogenous metabolite. Calcium Gluceptate Chemical Structure
  56. GC34036 Calcium polystyrene sulfonate Calcium polystyrene sulfonate is an ion-exchange resin used for reducing blood levels of potassium. Calcium polystyrene sulfonate Chemical Structure
  57. GC33841 Calf thymus DNA Calf thymus DNA (DNA from calf thymus) is high quality double-stranded template DNA isolated from the thymus of male and female calves. Calf thymus DNA Chemical Structure
  58. GC31703 CAM-IN-1 CAM-IN-1 is a potent and selective inhibitor of E-selectin and ICAM-1 with IC50 values of 7 and 5 nM, respectively. CAM-IN-1 Chemical Structure
  59. GC31811 Camobucol (AGIX 4207) Camobucol (AGIX 4207) (AGIX 4207) is an orally active, phenolic antioxidant and anti-inflammatory compound with antirheumatic properties. Camobucol (AGIX 4207) Chemical Structure
  60. GC13480 Camostat Mesilate Camostat Mesilate (Camostat mesilate) is an orally active, synthetic serine protease inhibitor for chronic pancreatitis. Camostat Mesilate Chemical Structure
  61. GC33138 Cancer-Targeting Compound 1 Cancer-Targeting Compound 1 is used in the research of hormone-?related cancer, extracted from patent WO 2008021331 A2. Cancer-Targeting Compound 1 Chemical Structure
  62. GC31308 Carabersat

    Carabersat is a potent anticonvulsant agent.

     Carabersat Chemical Structure
  63. GC16295 Carbadox

    antibiotic

     Carbadox Chemical Structure
  64. GC31273 Carbamic acid Carbamic acid is an agent for treating, one or more disorders or conditions wherein the dopaminergic system is disrupted, such as one or more disorders or conditions independently selected from the group consisting of: schizophrenia and other psychotic states; mood disorders ADHD; aggression; movement disorders. Carbamic acid Chemical Structure
  65. GC31968 Carbasalate calcium A calcium-urea chelate of aspirin Carbasalate calcium Chemical Structure
  66. GC32421 Carbazole derivative 1 Carbazole derivative 1 (2-Fluoro-7-[(3-pyridinyl)methyl]-9H-carbazole) is a carbazole derivative which can be used to reduce androgen or oestrogen levels in mammals, including humans. Carbazole derivative 1 Chemical Structure
  67. GC11419 Carbetocin oxytocin receptor agonist Carbetocin Chemical Structure
  68. GC12225 Carbidopa Decarboxylase inhibitor Carbidopa Chemical Structure
  69. GC11142 Carbimazole imidazole antithyroid agent Carbimazole Chemical Structure
  70. GC34430 Carboxy pyridostatin trifluoroacetate salt Carboxy pyridostatin trifluoroacetate salt has the peculiarity to exhibit high molecular specificity for RNA over DNA G4s. Carboxy pyridostatin trifluoroacetate salt Chemical Structure
  71. GC38067 Carcainium chloride Carcainium chloride (QX 572) is a quaternary derivative of Lidocaine. Carcainium chloride Chemical Structure
  72. GC34336 Carnostatine (SAN9812) Carnostatine (SAN9812) Chemical Structure
  73. GC38897 Carnostatine hydrochloride Carnostatine hydrochloride (SAN9812 hydrochloride) is a potent and selective carnosinase 1 (CN1) inhibitor with a Ki of 11 nM for human recombinant CN1. Carnostatine hydrochloride Chemical Structure
  74. GC33864 Carsalam (Carbonylsalicylamide) Carsalam (Carbonylsalicylamide) (Carbonylsalicylamide) is a nonsteroidal anti-inflammatory drug. Carsalam (Carbonylsalicylamide) Chemical Structure
  75. GC33576 Carzenide (4-Sulfamoylbenzoic acid) Carzenide (4-Sulfamoylbenzoic acid) is an organic synthesis intermediate, for synthetic drug. Carzenide (4-Sulfamoylbenzoic acid) Chemical Structure
  76. GC15997 Casanthranol Mixture of anthranol glycosides Casanthranol Chemical Structure
  77. GC34317 CB-6644 CB-6644 is a selective inhibitor of RUVBL1/2 complex with anti-cancer activity. CB-6644 blocks the ATPase activity of RUVBL1/2 with an IC50 of 15 nM. CB-6644 Chemical Structure
  78. GC15227 CB-839 CB-839 (CB-839) is a first-in-class, selective, reversible and orally active glutaminase 1 (GLS1) inhibitor. CB-839 selectively inhibits GLS1 splice variants KGA (kidney-type glutaminase) and GAC (glutaminase C) compared to GLS2. The IC50s are 23 nM and 28 nM for endogenous glutaminase in mouse kidney and brain, respectively. CB-839 inudces autophagy and has antitumor activity. CB-839 Chemical Structure
  79. GC13336 CBR-5884 selective inhibitor of PHGDH CBR-5884 Chemical Structure
  80. GC32893 CCF642 A PDI inhibitor CCF642 Chemical Structure
  81. GC16722 CE3F4 Uncompetitive Epac1 inhibitor CE3F4 Chemical Structure
  82. GC30227 Cenobamate S-Enantiomer Cenobamate S-Enantiomer Chemical Structure
  83. GC31771 Cephalosporin C zinc salt A cephalosporin antibiotic Cephalosporin C zinc salt Chemical Structure
  84. GC16301 Cetaben unique,PPARα-independent peroxisome proliferator Cetaben Chemical Structure
  85. GC31374 Cetilistat (ATL-962) Cetilistat (ATL-962) (ATL-962), an inhibitor of pancreatic lipase, acts as an effective anti-obesity agent. Cetilistat (ATL-962) Chemical Structure
  86. GC15892 Cetrimonium Bromide (CTAB) Cetrimonium Bromide (CTAB) (CTAB) is an amine based cationic quaternary surfactant, is one of the components of the topical antiseptic Cetrimide. Cetrimonium Bromide (CTAB) Chemical Structure
  87. GC10666 CGP 57380 MNK1 inhibitor, specific and selective CGP 57380 Chemical Structure
  88. GC30589 CGP 65015 CGP 65015 is an oral iron chelator, which can mobilize iron deposits. CGP 65015 Chemical Structure
  89. GC35677 Chitinase-IN-2 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. Chitinase-IN-2 Chemical Structure
  90. GC35678 Chitinase-IN-2 hydrochloride Chitinase-IN-2 hydrochloride is a insect chitinase and N- acetyl hexosaminidase inhibitor and pesticide; 50 uM/20uM compound concentration's inhibitory percentage are 98%/92% for chitinase/N- acetyl-hexosaminidase respectively. Chitinase-IN-2 hydrochloride Chemical Structure
  91. GC30906 Chloralose (α-Chloralose) Chloralose (α-Chloralose) Chemical Structure
  92. GC38306 Chloramben Chloramben (3-Amino-2,5-dichlorobenzoic acid) is a pre-emergence herbicide used to control the seedlings of annual grasses and broadleaf weeds. Chloramben Chemical Structure
  93. GC12908 Chlorambucil

    nitrogen mustard alkylating agent

     Chlorambucil Chemical Structure
  94. GC30169 Chloramine-T Chloramine-T is a titrimetric reagent, and an oxidizing agent. Chloramine-T Chemical Structure
  95. GC30656 Chlorantraniliprole An anthranilic diamide insecticide and ryanodine receptor agonist Chlorantraniliprole Chemical Structure
  96. GC31336 Chlorazanil Chlorazanil is a triazine derivative and also a new nonmercurial diuretic agent. Chlorazanil Chemical Structure
  97. GC31469 Chlorazanil hydrochloride Chlorazanil hydrochloride is a orally effective diuretic agent. Chlorazanil hydrochloride Chemical Structure
  98. GC30478 Chlorindanol (Clorindanol) Chlorindanol (Clorindanol) is a new antiseptic agent. Chlorindanol (Clorindanol) Chemical Structure
  99. GC16311 Chlormethiazole hydrochloride GABAA agonist Chlormethiazole hydrochloride Chemical Structure
  100. GC30190 Chlorophyllin sodium copper salt (Chlorophyllin copper sodium complex) Sodium copper chlorophyllin A is a semi-synthetic mixture of sodium copper salts derived from chlorophyll, primarily used as a food additive and in alternative medicine. Chlorophyllin sodium copper salt (Chlorophyllin copper sodium complex) Chemical Structure
  101. GC17732 Chloroprocaine HCl Chloroprocaine HCl (2-Chloroprocaine HCl) is a potent inhibitor of Na,K-ATPase activity with an IC50 of 13 mM. Chloroprocaine HCl Chemical Structure

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