1. Cat.No. Product Name Information
  2. GC35706 Cl-amidine Cl-amidine (N-α-benzoyl-N5-(2-chloro-1-iminoethyl)-l-ornithine amide), is a PAD4 inactivator with enhanced potency. Cl-amidine  Chemical Structure
  3. GC48807 (±)12(13)-EpOME MaxSpec® Standard (±)12(13)-EpOME MaxSpec® Standard  Chemical Structure
  4. GC91295 PPZ-A10

    An ionizable cationic lipid

    PPZ-A10  Chemical Structure
  5. GC69961 STING agonist-22

    STING agonist-22 (CF501) is an effective non-nucleotide STING agonist.

    STING agonist-22  Chemical Structure
  6. GK10026 Coomassie Blue Fast Staining Solution

    Coomassie Blue Fast Staining Solution can be used for polyacrylamide protein gel without pollution, fast, and high-sensitive staining. The minimum protein detection is 10 ng.

    Coomassie Blue Fast Staining Solution  Chemical Structure
  7. GC19278 Tis108 Strigolactone synthesis inhibitor  Tis108  Chemical Structure
  8. GC41452 Luteoloside A flavanoid with diverse biological activities Luteoloside  Chemical Structure
  9. GC65924 Lipopolysaccharides Lipopolysaccharides (LPS) is an endotoxin derived from the outer leaflet of the outer membrane of Gram-negative bacteria. Lipopolysaccharides consists of an antigen O-specific chain, a core oligosaccharide and lipid A. Lipopolysaccharides is a pathogenic associated molecular pattern (PAMP) that activates the immune system. Lipopolysaccharides activates TLR-4 on immune cells. This product is derived from Escherichia coli O55:B5. Lipopolysaccharides  Chemical Structure
  10. GC12645 Imiquimod maleate Immune response modifier Imiquimod maleate  Chemical Structure
  11. GC25314 CU-CPD107

    CU-CPD107 is a selective, dual-activity small-molecule which demonstrated differential activity against the TLR8 agonists and ssRNA ligands.

    CU-CPD107  Chemical Structure
  12. GC68897 CpG ODN 10101

    CpG ODN 10101 is a synthetic oligodeoxynucleotide (ODN) and a Toll-like receptor 9 (TLR9) agonist.

    CpG ODN 10101  Chemical Structure
  13. GC12439 Quinacrine (hydrochloride hydrate) voltage-dependent sodium channels blocker Quinacrine (hydrochloride hydrate)  Chemical Structure
  14. GC37081 Rebaudioside N

    Rebaudioside N is a minor steviol glycoside isolated from the leaves of Stevia rebaudiana Bertoni.

    Rebaudioside N  Chemical Structure
  15. GB50448 (2R,3S,4R,5R,6R)-6-(Methoxycarbonyl)tetrahydro-2H-pyran-2,3,4,5-tetrayltetraacetate (2R,3S,4R,5R,6R)-6-(Methoxycarbonyl)tetrahydro-2H-pyran-2,3,4,5-tetrayltetraacetate  Chemical Structure
  16. GB61555 Potassium ferrocyanide trihydrate


    Potassium ferrocyanide trihydrate  Chemical Structure
  17. GC15098 Trometamol proton acceptor used to treat acidemia Trometamol  Chemical Structure
  18. GC15676 Quinacrine 2HCl Anti-protozoal agent Quinacrine 2HCl  Chemical Structure
  19. GC26118 Dispase II

    Dispase, a neutral protease, is a non-specific metalloprotease, which is used to digest extracellular matrix from different tissues or organs, release and prepare primary single cells.

    Dispase II  Chemical Structure
  20. GC36103 Galanthamine hydrobromide Galanthamine hydrobromide  Chemical Structure
  21. GB10038 Creatine phosphokinase(Rabbit muscle, >150u/mg, Type I)

    Enzymes that catalyze the conversion of adenosine diphosphate (ADP) and phosphocreatine to ATP and creatine.

    Creatine phosphokinase(Rabbit muscle, >150u/mg, Type I)  Chemical Structure
  22. GC19516 1H,1H,2H,2H-Perfluoro-1-octanol 1H,1H,2H,2H-Perfluoro-1-octanol   Chemical Structure
  23. GC16736 Etomoxir Etomoxir  Chemical Structure
  24. GC35181 6''-O-Acetylglycitin 6''-O-Acetylglycitin, a acetyl glucoside, is one of the isoflavone isomer in soybeans, shows various extents of content reduction dependent on storage temperature, packaging condition, and its isoflavone isomer kind. 6''-O-Acetylglycitin  Chemical Structure
  25. GC25991 tetrathiomolybdate Tetrathiomolybdate (TM) is used in the clinic for the treatment of Wilson's disease by inducing dimerization of the metal-binding domain of the cellular copper efflux protein ATP7B (WLN4) through a unique sulfur-bridged Mo2S6O2 cluster. tetrathiomolybdate  Chemical Structure
  26. GC67669 Ammonium tetrathiomolybdate(VI) Ammonium tetrathiomolybdate(VI)  Chemical Structure
  27. GC19399 Derazantinib An inhibitor of FGFR Derazantinib  Chemical Structure
  28. GC47423 Heptaminol An aliphatic amine with cardiotonic and sympathomimetic activities Heptaminol  Chemical Structure
  29. GC10171 Puromycin aminonucleoside

    A glomerular epithelial cell toxin

    Puromycin aminonucleoside  Chemical Structure
  30. GC17550 A66 P110α inhibitor A66  Chemical Structure
  31. GC12604 Fumonisin B1 A PP5/PP2Cα/PP2A/PP1γ2/PP2B inhibitor Fumonisin B1  Chemical Structure
  32. GD22104 Tris(2,4,6-trimethoxyphenyl)phosphine Tris(2,4,6-trimethoxyphenyl)phosphine  Chemical Structure
  33. GC13671 Busulfan DNA alkylating agent Busulfan  Chemical Structure
  34. GC37074 Rebaudioside B Rebaudioside B is the minor constituent isolated from the leaves of Stevia rebaudiana Bertoni. Rebaudioside B  Chemical Structure
  35. GC26274 IR-117-17

    IR-117-17 is an ionizable cationic and biodegradable amino lipid.

    IR-117-17  Chemical Structure
  36. GC16892 XL-888 An orally bioavailable Hsp90 inhibitor XL-888  Chemical Structure
  37. GA20558 Ac-Gln-Gln-OH NAGG, precursor of the bacterial osmoprotectant N-acetylglutaminylglutamine amide (NAGGN). Ac-Gln-Gln-OH  Chemical Structure
  38. GC13055 Mocetinostat (MGCD0103, MG0103) An orally available HDAC inhibitor Mocetinostat (MGCD0103, MG0103)  Chemical Structure
  39. GC65516 Bemarituzumab Bemarituzumab is a first-in-class, humanized IgG1 monoclonal antibody against FGFR2b (a FGF receptor). Bemarituzumab blocks fibroblast growth factors from binding and activating FGFR2b. Bemarituzumab has the potential for cancer research. Bemarituzumab  Chemical Structure
  40. GA22068 H-Arg-Arg-OH Arginine-containing dipeptides as RR and RF (G-1515) are used by nitric oxide synthase as substrates in place of Arg. H-Arg-Arg-OH  Chemical Structure
  41. GC11719 HG-9-91-01

    HG-9-91-01 is a salt-inducible kinases (SIK) inhibitor, inhibited SIK1, SIK2, SIK3 with IC50 values of 0.92nM, 6.5nM and 19.4nM, respectively. HG-9-91-01  Chemical Structure

  42. GC15164 PND-1186 A potent FAK inhibitor PND-1186  Chemical Structure
  43. GF41712 2-(3-Bromophenyl)dibenzo[b,d]furan 2-(3-Bromophenyl)dibenzo[b,d]furan  Chemical Structure
  44. GC66145 Azido-PEG1-amine Azido-PEG1-amine is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. Azido-PEG1-amine  Chemical Structure
  45. GC63819 Asenapine maleate Asenapine maleate is a 5-HT (1A, 1B, 2A, 2B, 2C, 5A, 6, 7) and D2 antagonist with Ki values of 0.03-4.0 nM, 1.3nM, respectively, and an antipsychotic. Asenapine maleate  Chemical Structure
  46. GC39115 Terpinen-4-ol Terpinen-4-ol (4-Carvomenthenol), a naturally occurring monoterpene, is the main bioactive component of tea-tree oil. Terpinen-4-ol  Chemical Structure
  47. GC19275 Paritaprevir A HCV NS3/4A protease inhibitor Paritaprevir  Chemical Structure
  48. GB60264 N-tert-Butylbenzenesulfinimidoyl Chloride N-tert-Butylbenzenesulfinimidoyl Chloride  Chemical Structure
  49. GD14329 2,2,3,4,4,4-Hexafluoro-1-butanol 2,2,3,4,4,4-Hexafluoro-1-butanol  Chemical Structure
  50. GK10008 Ultra High Sensitivity ECL Kit Luminol-based chemiluminescent kit for detection of horseradish peroxidase (HRP)-labeled antibodies and their associated antigens Ultra High Sensitivity ECL Kit  Chemical Structure
  51. GF11402 Fmoc-His(Clt)-OH Fmoc-His(Clt)-OH  Chemical Structure
  52. GC14024 DL-AP3 A metabotropic glutamate receptor antagonist DL-AP3  Chemical Structure
  53. GC70125 Vosoritide acetate

    Vosoritide (BMN 111) acetate is a natriuretic peptide receptor 2 (NPR2) agonist that can stimulate the proliferation and differentiation of chondrocytes, promoting bone growth.

    Vosoritide acetate  Chemical Structure
  54. GC25736 Phycocyanobilin

    Phycocyanobilin (PCB) is an open-chain tetrapyrrole chromophore covalently bonded to both polypeptide chains of C-Phycocyanin (C-PC), the most represented biliprotein of Spirulina platensis, the mechanisms by which it protected cells included the reduction of oxidative stress damage, which could contribute to its clinical efficacy for the treatment of neurodegenerative diseases.This product has poor solubility, animal experiments are available, cell experiments please choose carefully!

    Phycocyanobilin  Chemical Structure
  55. GC63978 ML089

    ML089 is a potent, selective, and orally available phosphomannose isomerase (PMI) inhibitor with an IC50 of 1.3 ?M.

    ML089  Chemical Structure
  56. GC26273 α-Amylase, heat-stable (BR, 40000u/g)

    α-Amylase(heat-stable) (from Bacillus licheniformis), is widely used in various fermentation industries. This product is provided in solution form, with an enzyme activity of ≥500U/ml. The effective pH range of α-Amylase(heat-stable) is 5.5-8.0, with an optimal pH range of 5.8-6.5.

    α-Amylase, heat-stable (BR, 40000u/g)  Chemical Structure
  57. GC44152 MEGA-8

    MEGA-8 is a nonionic detergent that can be used to solubilize membrane proteins.

    MEGA-8  Chemical Structure
  58. GC14062 EPZ-6438 A EZH2 inhibitor,potent and selective EPZ-6438  Chemical Structure
  59. GC15289 Polymyxin B (sulfate) bactericidal activity against major multidrug-resistant Gram-negative bacteria. Polymyxin B (sulfate)  Chemical Structure
  60. GC26272 Mersalyl

    Mersalyl (Salirgan) is a potent vascular endothelial growth factor (VEGF) and hypoxia-inducible factor 1 (HIF-1) inducer.

    Mersalyl  Chemical Structure
  61. GC10396 S-Adenosylhomocysteine S-adenosylhomocysteine (SAH), an amino acid derivative, is a key intermediate metabolite in methionine metabolism[1]. S-Adenosylhomocysteine  Chemical Structure
  62. GD00205 Amberlite® IRA-410 ion-exchange resin Amberlite® IRA-410 ion-exchange resin  Chemical Structure
  63. GC36159 Glycerol 3-phosphate Glycerol 3-phosphate is produced by cytosolic glycerol 3-phosphate dehydrogenase pathway through the reduction of dihydroxyacetone phosphate using NADH formed during glycolysis. Glycerol 3-phosphate  Chemical Structure
  64. GC61482 sn-Glycerol 3-phosphate lithium sn-Glycerol 3-phosphate lithium is produced by cytosolic glycerol 3-phosphate dehydrogenase pathway through the reduction of dihydroxyacetone phosphate using NADH formed during glycolysis. sn-Glycerol 3-phosphate lithium  Chemical Structure
  65. GN20145 5'-Biotin-G-Monophosphate

    5’-Biotin-G-Monophosphate allows for the incorporation of biotin at the 5’ terminus of RNA, 

    5'-Biotin-G-Monophosphate  Chemical Structure
  66. GC19589 Collagenase I The collagenase currently has approximately four types: Type I collagenase, Type II collagenase, Type III collagenase, and Type IV collagenase. Collagenase I  Chemical Structure
  67. GC48293 α-Pyrrolidino-2-phenylacetophenone (hydrochloride) An Analytical Reference Standard α-Pyrrolidino-2-phenylacetophenone (hydrochloride)  Chemical Structure
  68. GC52208 5-fluoro ADB-5'Br-PINACA An Analytical Reference Standard 5-fluoro ADB-5'Br-PINACA  Chemical Structure
  69. GC16929 8-Bromo-cAMP, sodium salt Cell-permeable cAMP analog that activates PKA 8-Bromo-cAMP, sodium salt  Chemical Structure
  70. GC19987 AFUBIATA An Analytical Reference Standard AFUBIATA  Chemical Structure
  71. GC34470 AMXT-1501 tetrahydrochloride AMXT-1501 tetrahydrochloride is an orally active polyamine transport inhibitor. AMXT-1501 tetrahydrochloride  Chemical Structure
  72. GC31432 Asp-AMS Asp-AMS, an analogue of aspartyl-adenylate, is an aspartyl-tRNA synthetase inhibitor and also a strong competitive inhibitor of the mitochondrial enzyme. Asp-AMS  Chemical Structure
  73. GC42945 bk-2C-B (hydrochloride)

    A series of 2,5-dimethoxyphenethylamines, substituted at the four position of the aromatic ring, have psychoactive effects.

    bk-2C-B (hydrochloride)  Chemical Structure
  74. GC31655 Cholera toxin (choleragen) Cholera toxin (choleragen) is an enterotoxogenic protein complex consisting of a single A subunit (cholera toxin A subunit (CTA)) and a pentamer of B subunits (cholera toxin B subunit (CTB)). Cholera toxin (choleragen)  Chemical Structure
  75. GC47116 Coenzyme Q10-d6 An internal standard for the quantification of CoQ10 Coenzyme Q10-d6  Chemical Structure
  76. GC65550 Danavorexton Danavorexton is an orexin receptor agonist. Danavorexton  Chemical Structure
  77. GC66407 Etokimab Etokimab (Antibody ANB 020) is a humanized monoclonal antibody that targets IL-33. Etokimab can be used for the research of atopic dermatitis. Etokimab  Chemical Structure
  78. GC64281 Evolocumab

    Evolocumab (AMG 145) is a human monoclonal antibody that inhibits PCSK9.

    Evolocumab  Chemical Structure
  79. GM10002 Fluc mRNA(5’CAP)

    Fluc mRNA (5'CAP) is labeled luciferase mRNA produced by in vitro transcription and has a Cap 1 cap structure and a poly(A) tail.

    Fluc mRNA(5’CAP)  Chemical Structure
  80. GC19597 Hydrogenated Soybean Phospholipids Hydrogenated lecithin Hydrogenated Soybean Phospholipids  Chemical Structure
  81. GC67690 JBJ-09-063 hydrochloride JBJ-09-063 hydrochloride is a mutation selective allosteric EGFR inhibitor JBJ-09-063 hydrochloride  Chemical Structure
  82. GC10181 L-803,087 trifluoroacetate somatostatin sst4 receptor agonist L-803,087 trifluoroacetate  Chemical Structure
  83. GC64338 LYP-IN-1 LYP-IN-1 is a potent, selective and specific LYP inhibitor with a Ki and an IC50 of 110 nM and 0.259 μM, respectively. LYP-IN-1  Chemical Structure
  84. GC52234 MDMB-5'Br-BUTINACA An Analytical Reference Standard MDMB-5'Br-BUTINACA  Chemical Structure
  85. GC14391 Moxalactam (sodium salt) β-lactam antibiotic Moxalactam (sodium salt)  Chemical Structure
  86. GC64295 MS67 MS67 is a potent and selective WD40 repeat domain protein 5 (WDR5) degrader with a Kd of 63 nM. MS67 is inactive against other protein methyltransferases, kinases, GPCRs, ion channels, and transporters. MS67 shows potent acticancer effects. MS67  Chemical Structure
  87. GC44284 N1,N8-Diacetylspermidine (hydrochloride) N1,N8-Diacetylspermidine is a diacetylated derivative of spermidine, a natural polyamine. N1,N8-Diacetylspermidine (hydrochloride)  Chemical Structure
  88. GC67929 Orexin 2 Receptor Agonist 2 Orexin 2 Receptor Agonist 2 is a selective orexin 2 receptor agonist. Orexin 2 Receptor Agonist 2  Chemical Structure
  89. GC63287 Pyrrolnitrin Pyrrolnitrin is an antibiotic isolated from Pseudomonas pyrrocinia. Pyrrolnitrin  Chemical Structure
  90. GC37571 Rubitecan A DNA topoisomerase I inhibitor Rubitecan  Chemical Structure
  91. GC62691 SG3199 SG3199 is a cytotoxic DNA minor groove interstrand crosslinking pyrrolobenzodiazepine (PBD) dimer. SG3199 is the released warhead component of the ADC payload Tesirine (SG3249). SG3199  Chemical Structure
  92. GC50098 TC-T 6000 TC-T 6000 is a potent and selective human ENT4 (equilibrative nucleoside transporter 4) inhibitor with an IC50 of 74.4 nM. TC-T 6000  Chemical Structure
  93. GC64862 Tricetin Tricetin is a potent competitive inhibitor of the Keap1-Nrf2 Protein Protein Interaction (PPI). Tricetin  Chemical Structure
  94. GC64727 Tris-NTA Tris-NTA is a His-tagged protein ligand, which can be used to bind His-tagged proteins. Tris-NTA  Chemical Structure
  95. GC19369 Vaborbactam Vaborbactam is a cyclic boronic acid pharmacophore β-lactamase inhibitor. Vaborbactam  Chemical Structure
  96. GA23909 Z-Phe-Phe-diazomethylketone Z-FF-DMK, a cathepsin L-selective inhibitor. Z-Phe-Phe-diazomethylketone  Chemical Structure
  97. GB61565 Tetrasodium pyrophosphate Tetrasodium pyrophosphate  Chemical Structure
  98. GC19889 Bovine Serum Albumin (Fatty acid Free)

    Bovine Serum Albumin (Fatty acid Free)  Chemical Structure
  99. GB20003 Pseudo-UTP,100mM Tris Solution A modified nucleoside-5’-O-triphosphate, commonly used for drugable mRNA synthesis Pseudo-UTP,100mM Tris Solution  Chemical Structure
  100. GA23511 Spexin Spexin (SPX, also called NPQ) is a gastro-intestinal peptide hormone. In situ hybridization localized its mRNA to the stomach and esophagus. Synthetic spexin induced dose-dependent contraction of stomach muscle, suggesting that it is involved in digestion. The results obtained by Rucinski et al. indicate that spexin may inhibit adrenocortical cell proliferation. Spexin  Chemical Structure
  101. GC67796 Sorbicillin Sorbicillin  Chemical Structure

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