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Home >> Infectious Disease

Infectious Disease

Products for  Infectious Disease

  1. Cat.No. Product Name Information
  2. GC52351 Citrullinated α-Enolase (R8 + R14) (1-19)-biotin Peptide A biotinylated and citrullinated α-enolase peptide Citrullinated α-Enolase (R8 + R14) (1-19)-biotin Peptide Chemical Structure
  3. GC66467 Claficapavir Claficapavir (A1752) is a specific nucleocapsid protein (NC) inhibitor with an IC50 around 1 μM. Claficapavir strongly binds the HIV-1 NC (Kd=20 nM) thereby inhibiting the chaperone properties of NC and leading to good antiviral activity against the HIV-1. Claficapavir Chemical Structure
  4. GC49852 Clindamycin (hydrochloride hydrate) Clindamycin (hydrochloride hydrate) is an oral protein synthesis inhibitory agent that has the ability to suppress the expression of virulence factors in Staphylococcus aureus at sub-inhibitory concentrations (sub-MICs). Clindamycin (hydrochloride hydrate) Chemical Structure
  5. GC43278 Clindamycin Sulfoxide Clindamycin sulfoxide is an active metabolite of the antibiotic clindamycin. Clindamycin Sulfoxide Chemical Structure
  6. GC52171 Clindamycin-d3 (hydrochloride) Clindamycin-d3 (hydrochloride) is the deuterium labeled Clindamycin. Clindamycin-d3 (hydrochloride) Chemical Structure
  7. GC47105 Clonostachydiol A fungal metabolite with anticancer and anthelmintic activities Clonostachydiol Chemical Structure
  8. GC47109 Clotrimazole-d5 An internal standard for the quantification of clotrimazole Clotrimazole-d5 Chemical Structure
  9. GC49096 Cobaltic Protoporphyrin IX (chloride) An inducer of HO-1 activity Cobaltic Protoporphyrin IX (chloride) Chemical Structure
  10. GC43298 Colistin Colistin is a complex antibiotic containing greater than 30 components, with the cyclic polypeptide antibiotics polymyxins E1 (colistin A) and E2 (colistin B) as the major components. Colistin Chemical Structure
  11. GC46122 Collinin A coumarin with diverse biological activities Collinin Chemical Structure
  12. GC43314 Corynecin I Corynecin I is a chloramphenicol-like antibiotic originally isolated from Corynebacterium. Corynecin I Chemical Structure
  13. GC40079 Corynecin II Corynecin II is a chloramphenicol-like antibiotic originally isolated from Corynebacterium. Corynecin II Chemical Structure
  14. GC40083 Corynecin III Corynecin III is a chloramphenicol-like antibiotic originally isolated from Corynebacterium. Corynecin III Chemical Structure
  15. GC47121 Cotrimoxazole A mixture of the antibiotics sulfamethoxazole and trimethoprom Cotrimoxazole Chemical Structure
  16. GC47122 Coumaphos An organophosphate pesticide Coumaphos Chemical Structure
  17. GC25306 CQ31

    CQ31, a small molecule, selectively activates caspase activation and recruitment domain-containing 8 (CARD8).

     CQ31 Chemical Structure
  18. GC47128 CU-32 A cGAS inhibitor CU-32 Chemical Structure
  19. GC47129 CU-76 A cGAS inhibitor CU-76 Chemical Structure
  20. GC49557 Cu-GTSM A copper-containing compound with diverse biological activities Cu-GTSM Chemical Structure
  21. GC64348 Cyanidin 3-sambubioside chloride Cyanidin 3-sambubioside chloride (Cyanidin-3-O-sambubioside chloride), a major anthocyanin, a natural colorant, and is a potent NO inhibitor. Cyanidin 3-sambubioside chloride Chemical Structure
  22. GC49821 Cyclamidomycin A bacterial metabolite with antibiotic activity Cyclamidomycin Chemical Structure
  23. GC43339 Cyclic di-AMP (sodium salt) Cyclic di-AMP (c-di-AMP) is a second messenger produced by bacteria but not by mammals. Cyclic di-AMP (sodium salt) Chemical Structure
  24. GC19526 Cyclic di-GMP (sodium salt) Cyclic di-GMP (sodium salt) is a STING agonist and a bacterial second messenger that coordinates different aspects of bacterial growth and behavior, including motility, virulence, biofilm formation, and cell cycle progression. Cyclic di-GMP (sodium salt) has anti-cancer cell proliferation activity and also induces elevated CD4 receptor expression and cell cycle arrest. Cyclic di-GMP (sodium salt) can be used in cancer research. Cyclic di-GMP (sodium salt) Chemical Structure
  25. GC43340 Cyclic di-IMP (sodium salt) Cyclic di-IMP (sodium salt) (c-di-IMP) is a synthetic second messenger structurally related to the bacterial second messengers cyclic di-GMP and cyclic di-AMP. Cyclic di-IMP (sodium salt) Chemical Structure
  26. GC48397 Cyclic di-UMP (sodium salt) A pyrimidine-containing CDN Cyclic di-UMP (sodium salt) Chemical Structure
  27. GC41176 Cyclo(δ-Ala-L-Val) Cyclo(δ-Ala-L-Val) is a bacterial cyclic dipeptide characterized as a diketopiperazine. Cyclo(δ-Ala-L-Val) Chemical Structure
  28. GC43342 Cyclo(L-Leu-L-Pro) Cyclo(L-Leu-L-Pro) is a diketopiperazine metabolite that has been isolated from various bacterial and fungal species including Streptomyces. Cyclo(L-Leu-L-Pro) Chemical Structure
  29. GC18488 Cyclo(L-Leu-L-Trp) Cyclo(L-Leu-L-Trp) is a diketopiperazine metabolite originally isolated from Penicillium. Cyclo(L-Leu-L-Trp) Chemical Structure
  30. GC41555 Cyclo(L-Phe-L-Val) Cyclo(L-Phe-L-Val) is a metabolite of the sponge bacterium Pseudoalteromonas sp. Cyclo(L-Phe-L-Val) Chemical Structure
  31. GC18268 Cyclo(L-Trp-L-Trp) Cyclo(L-Trp-L-Trp) is a cyclic dipeptide that has been used as a substrate for indole prenyltransferases in the synthesis of mono- and diprenylated indolines. Cyclo(L-Trp-L-Trp) Chemical Structure
  32. GC40569 Cyclopenin Cyclopenin is an inhibitor of acetylcholinesterase (AChE; IC50 = 2.04 μM for human recombinant AChE) that is produced by Penicillium. Cyclopenin Chemical Structure
  33. GC64068 Cyclotriazadisulfonamide Cyclotriazadisulfonamide (CADA) is a specific CD4-targeted HIV entry inhibitors. Cyclotriazadisulfonamide Chemical Structure
  34. GC43368 D,L-1′-Acetoxychavicol Acetate D,L-1′-Acetoxychavicol acetate is a natural compound first isolated from the rhizomes of ginger-like plants. D,L-1′-Acetoxychavicol Acetate Chemical Structure
  35. GC49792 D-(+)-Cellopentaose D-(+)-Cellopentaose is a penta oligosaccharide of cellulose. D-(+)-Cellopentaose Chemical Structure
  36. GC40294 D-Eritadenine D-Eritadenine is an adenosine analog and a potent, reversible inhibitor of S-adenosylhomocysteine hydrolase (SAAH; IC50 = 7 nM). D-Eritadenine Chemical Structure
  37. GC49378 D-Glutamic Acid-d5 An internal standard for the quantification of D-glutamic acid D-Glutamic Acid-d5 Chemical Structure
  38. GC47246 D-Lysine lactam A chiral building block D-Lysine lactam Chemical Structure
  39. GC47266 D-Ornithine lactam A building block D-Ornithine lactam Chemical Structure
  40. GC47270 D-Pyroaspartic Acid A synthetic intermediate D-Pyroaspartic Acid Chemical Structure
  41. GC46124 D13 An acylhydrazone antifungal D13 Chemical Structure
  42. GC45883 Daclatasvir-d6 An internal standard for the quantification of daclatasvir Daclatasvir-d6 Chemical Structure
  43. GC43386 DDD85646

    DDD85646 is a moderately bioavailable pyrazole sulphonamide inhibitor of T.

     DDD85646 Chemical Structure
  44. GC64391 DDX3-IN-2 DDX3-IN-2 is an active DEADbox polypeptide 3 (DDX3) inhibitor with an IC50 value of 0.3 μM. DDX3-IN-2 Chemical Structure
  45. GC52191 Deacetylanisomycin Deacetylanisomycin is a potent growth regulator in plants and an inactive derivative of Anisomycin. Deacetylanisomycin Chemical Structure
  46. GC43390 Deacetylravidomycin Deacetylravidomycin is a microbial metabolite that has been found in Streptomyces and has light-dependent antibiotic and anticancer activities. Deacetylravidomycin Chemical Structure
  47. GC64270 Decanoyl-RVKR-CMK TFA Decanoyl-RVKR-CMK (DecRVKRcmk) TFA inhibits over-expressed gp160 processing and HIV-1 replication. Decanoyl-RVKR-CMK TFA Chemical Structure
  48. GC43394 Decatromicin B Decatromicin B is a bacterial metabolite that has been found in Actinomadura. Decatromicin B Chemical Structure
  49. GC43395 Deethylindanomycin Deethylindanomycin is a polyether antibiotic that has been found in S. Deethylindanomycin Chemical Structure
  50. GC43398 Defensin HNP-3 (human) (trifluoroacetate salt) Defensin HNP-3 is a peptide secreted by human polymorphonuclear leukocytes (PMNs) that has antimicrobial properties. Defensin HNP-3 (human) (trifluoroacetate salt) Chemical Structure
  51. GC43408 Deoxycholic Acid (sodium salt hydrate) Deoxycholic acid (cholanoic acid) sodium hydrate，a bile acid, is a by-product of intestinal metabolism, that activates the G protein-coupled bile acid receptorTGR5. Deoxycholic Acid (sodium salt hydrate) Chemical Structure
  52. GC47187 Deoxycholic Acid-d4 A quantitative analytical standard guaranteed to meet MaxSpec® identity, purity, stability, and concentration specifications Deoxycholic Acid-d4 Chemical Structure
  53. GC18869 Deoxyenterocin Deoxyenterocin is a bacterial metabolite originally isolated from Streptomyces that has diverse biological activities, including antibiotic, antiviral, and antioxidant properties. Deoxyenterocin Chemical Structure
  54. GC41092 Deoxyfusapyrone Deoxyfusapyrone is an α-pyrone fungal metabolite originally isolated from F. Deoxyfusapyrone Chemical Structure
  55. GC40654 Deoxyviolacein Deoxyviolacein is a bacterial metabolite and byproduct in the biosynthesis of the bisindole alkaloid violacein that has anticancer, antibacterial, and antifungal properties. Deoxyviolacein Chemical Structure
  56. GC49115 Desacetylcefotaxime (potassium salt) An active metabolite of cefotaxime Desacetylcefotaxime (potassium salt) Chemical Structure
  57. GC43417 Desertomycin A Desertomycin A is fungal metabolite and the major component of the desertomycin antibiotic complex that has been found in S. Desertomycin A Chemical Structure
  58. GC43418 Desethylene Ciprofloxacin (hydrochloride) Desethylene ciprofloxacin is a major metabolite of ciprofloxacin. Desethylene Ciprofloxacin (hydrochloride) Chemical Structure
  59. GC49100 Desmethyl Ofloxacin (hydrochloride) A metabolite of ofloxacin Desmethyl Ofloxacin (hydrochloride) Chemical Structure
  60. GC43424 Desotamide Desotamide is a cyclic hexapeptide antibiotic originally isolated from Streptomyces. Desotamide Chemical Structure
  61. GC46130 Destruxin B2 A mycotoxin with antiviral, insecticidal, and phytotoxic activities Destruxin B2 Chemical Structure
  62. GC45992 Diallyl Tetrasulfide An organosulfur compound with diverse biological activities Diallyl Tetrasulfide Chemical Structure
  63. GC49153 Didemnin B Didemnin B is a cyclic depsipeptide produced by marine tunicates that specifically binds the GTP-bound conformation of EEF1A. Didemnin B Chemical Structure
  64. GC45662 Dieugenol A neolignan with antioxidative and antiparasitic activities Dieugenol Chemical Structure
  65. GC47220 Difloxacin-d3 An internal standard for the quantification of difloxacin Difloxacin-d3 Chemical Structure
  66. GC40063 Dihydroaeruginoic Acid Dihydroaeruginoic acid is an antibiotic originally isolated from P. Dihydroaeruginoic Acid Chemical Structure
  67. GC47228 Dihydronovobiocin A coumarin antibiotic Dihydronovobiocin Chemical Structure
  68. GC41162 Dihydropleuromutilin Dihydropleuromutilin is a semisynthetic antibiotic and derivative of pleuromutilin. Dihydropleuromutilin Chemical Structure
  69. GC43467 Dimethyldioctadecylammonium (bromide) Dimethyldioctadecylammonium (DDA) is a cationic amphipathic lipid. Dimethyldioctadecylammonium (bromide) Chemical Structure
  70. GC52082 Dimidium (bromide) A trypanocide Dimidium (bromide) Chemical Structure
  71. GC43488 DL-erythro/threo Sphinganine (d16:0) DL-erythro/threo Sphinganine (d16:0) is a sphingolipid that is decreased in rats following long-term, low-dose administration of dimethoate and is used as a biomarker for dimethoate exposure. DL-erythro/threo Sphinganine (d16:0) Chemical Structure
  72. GC49383 DL-Phenyl-d5-alanine An internal standard for the quantification of DL-phenylalanine DL-Phenyl-d5-alanine Chemical Structure
  73. GC52120 DMPE-MPEG(2000) A PEGylated form of DMPE DMPE-MPEG(2000) Chemical Structure
  74. GC45995 DO264 An ABHD12 inhibitor DO264 Chemical Structure
  75. GC47257 Dodecanoyl D-Sucrose A nonionic surfactant Dodecanoyl D-Sucrose Chemical Structure
  76. GC52095 Dodecyltrimethylammonium (bromide) A cationic surfactant Dodecyltrimethylammonium (bromide) Chemical Structure
  77. GC43562 Doramectin aglycone Doramectin aglycone is an acid degradation product of doramectin, a disaccharide-containing anthelmintic that potentiates glutamate- and GABA-gated chloride channel opening in nematodes, and its acid-catalyzed hydrolysis product doramectin monosaccharide. Doramectin aglycone Chemical Structure
  78. GC43563 Doramectin monosaccharide Doramectin monosaccharide is an acid degradation product of doramectin, a disaccharide-containing anthelmintic that potentiates glutamate- and GABA-gated chloride channel opening in nematodes. Doramectin monosaccharide Chemical Structure
  79. GC46135 Drimendiol A sesquiterpene Drimendiol Chemical Structure
  80. GC43572 Drimentine A Drimentine A is a terpenylated diketopiperazine antibiotic originally isolated from Actinomycete bacteria. Drimentine A Chemical Structure
  81. GC40082 Drimentine B Drimentine B is a terpenylated diketopiperazine antibiotic originally isolated from Actinomycete bacteria. Drimentine B Chemical Structure
  82. GC40059 Echinocandin B Echinocandin B is an echinocandin antifungal originally isolated from Aspergillus. Echinocandin B Chemical Structure
  83. GC47279 Echinosporin A bacterial metabolite with antibacterial and anticancer activities Echinosporin Chemical Structure
  84. GC43588 EGA EGA is an inhibitor of endosomal trafficking. EGA Chemical Structure
  85. GC18191 Elastatinal

    Elastatinal is a potent inhibitor of pancreatic elastase (Ki = 240 nM) that is produced by various species of Actinomycetes.

     Elastatinal Chemical Structure
  86. GC63987 Eleutheroside B1

    Eleutheroside B1, a coumarin compound, has a wide spectrum of anti-human influenza virus efficacy, with an IC50 value of 64-125μg/ml.

     Eleutheroside B1 Chemical Structure
  87. GC48546 Emeguisin A A fungal metabolite Emeguisin A Chemical Structure
  88. GC46137 Emestrin A mycotoxin Emestrin Chemical Structure
  89. GC64484 Emivirine Emivirine (MKC-442) is a non-nucleoside reverse transcriptase inhibitors (NNRTIs) with Ki values of 0.20 and 0.01 μM for dTTP- and dGTP-dependent DNA or RNA polymerase activity, respectively. Emivirine Chemical Structure
  90. GC43612 Enopeptin A Enopeptin A, originally isolated from a culture broth of Streptomyces sp. Enopeptin A Chemical Structure
  91. GC52334 ENPP1 Inhibitor 4e An ENPP1 inhibitor ENPP1 Inhibitor 4e Chemical Structure
  92. GC49101 Enrofloxacin-d5 An internal standard for the quantification of enrofloxacin Enrofloxacin-d5 Chemical Structure
  93. GC52261 Entecavir-d2 An internal standard for the quantification of entecavir Entecavir-d2 Chemical Structure
  94. GC47295 Enviroxime An antiviral agent Enviroxime Chemical Structure
  95. GC41326 Epioxytetracycline Epioxytetracycline, the degradation product of Oxytetracycline (OTC), can be found in swine manure compost and wastewater. Epioxytetracycline Chemical Structure
  96. GC40845 Eprinomectin B1a Eprinomectin B1a is a major component (>90%) of the antiparasitic compound eprinomectin, which also contains eprinomectin B1b and belongs to the avermectin family of insecticides and anthelmintics. Eprinomectin B1a Chemical Structure
  97. GC43622 Eprinomectin B1b Eprinomectin B1b is a minor component and belongs to the avermectin family of insecticides and anthelmintics. Eprinomectin B1b Chemical Structure
  98. GC48372 Erythromycin 2'-Propionate An antibiotic Erythromycin 2'-Propionate Chemical Structure
  99. GC43626 Erythromycin A N-oxide Erythromycin A N-oxide is a potential impurity found in commercial preparations of erythromycin. Erythromycin A N-oxide Chemical Structure
  100. GC18499 Erythromycin C Erythromycin C is an intermediate in the biosynthesis of erythromycin . Erythromycin C Chemical Structure
  101. GC43627 Erythromycin lactobionate A macrolide antibiotic Erythromycin lactobionate Chemical Structure

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