Home >> Signaling Pathways >> Microbiology & Virology

Microbiology & Virology

Microbiology & Virology

Microbiology & Virology

A virus is a small infectious agent that replicates inside living cells. Viruses cause many human diseases from small illnesses, like influenza, to more deadly diseases, like hepatitis B and HIV. Our body’s immune system defends against viral infection by generating specific antibodies to bind to and neutralize viral particles and by cell mediated immunity that destroys infected host cells.

Targets for  Microbiology & Virology

Products for  Microbiology & Virology

  1. Cat.No. Product Name Information
  2. GC39580 Ceftezole sodium Ceftezole sodium (CTZ sodium) is a broad-spectrum cephem antibiotic against many species of gram-positive and gram-negative bacteria. Ceftezole sodium  Chemical Structure
  3. GC15695 Ceftibuten third-generation cephalosporin antibiotic Ceftibuten  Chemical Structure
  4. GC35647 Ceftibuten dihydrate

    SCH 39720

    Ceftibuten (Sch-39720) dihydrate, an antibiotic, is an orally active cephalosporin, possesses potent activity in vitro against a wide range of gram-negative and certain gram-positive pathogens. Ceftibuten dihydrate  Chemical Structure
  5. GC11235 Ceftiofur HCl

    U-64279A, U-67279A

    Ceftiofur HCl is a semisynthetic antibiotic, with activity against various gram-positive and gram-negative, aerobic and anaerobic bacteria encountered by domestic animals. Ceftiofur HCl  Chemical Structure
  6. GC32159 Ceftiofur sodium (sodium ceftiofur) Ceftiofur sodium (sodium ceftiofur) is an antibiotic of the cephalosporin type (third generation), licensed for use in veterinary medicine. Ceftiofur sodium (sodium ceftiofur)  Chemical Structure
  7. GC32229 Ceftizoxime Ceftizoxime is a bacterial inhibitor which acts by interfering with bacterial cell wall synthesis and inhibiting cross-linking of the peptidoglycan. Ceftizoxime  Chemical Structure
  8. GC32180 Ceftizoxime sodium (SKF-88373)

    FR 13479

    Ceftizoxime sodium (SKF-88373) (SKF-88373) is third generation cephalosporin effective against Gram-negative and Gram-positive bacteria. Ceftizoxime sodium (SKF-88373)  Chemical Structure
  9. GC32128 Ceftobiprole (Ro 63-9141) Ceftobiprole (Ro 63-9141) (Ro 63-9141) is a broad-spectrum cephalosporin with high levels of in vitro activity against methicillin- (MRSA) and vancomycin-resistant staphylococci (VRSA) and penicillin-resistant streptococci with a MIC90 value of 2 μg/mL for MRSA. Ceftobiprole (Ro 63-9141)  Chemical Structure
  10. GC68005 Ceftobiprole medocaril sodium Ceftobiprole medocaril sodium  Chemical Structure
  11. GC71542 Ceftolozane Ceftolozane (CXA-101 free base; FR264205 free base) is a cephalosporin antibiotic with potent activity againstPseudomonas aeruginosa and strains Enterobacteriaceae, with MICs of 0.5 and 0.25-0.5 mg/L. Ceftolozane  Chemical Structure
  12. GC35648 Ceftriaxone Ceftriaxone is a third-generation cephalosporin antibiotic with excellent activity against many gram-negative, and reasonable activity against most gram-positive microorganisms. Ceftriaxone  Chemical Structure
  13. GC32075 Ceftriaxone sodium salt (Disodium ceftriaxone) Ceftriaxone sodium salt (Disodium ceftriaxone) (Disodium ceftriaxone) is a third-generation cephalosporin antibiotic with excellent activity against many gram-negative, and reasonable activity against most gram-positive microorganisms. Ceftriaxone sodium salt (Disodium ceftriaxone)  Chemical Structure
  14. GC11349 Ceftriaxone Sodium Trihydrate

    Ceftriaxone disodium hemiheptahydrate, Ro 13-9904, Rosihlitazone

    Ceftriaxone Sodium Trihydrate (Ceftriaxone disodium hemiheptahydrate) is a third-generation cephalosporin antibiotic with excellent activity against many gram-negative, and reasonable activity against most gram-positive microorganisms. Ceftriaxone Sodium Trihydrate  Chemical Structure
  15. GC71669 Ceftriaxone-d3 disodium Ceftriaxone-d3 (disodium) is the deuterium labeled Ceftriaxone. Ceftriaxone-d3 disodium  Chemical Structure
  16. GC33998 Cefuracetime (SKF81367) SKF81367 is a cephalosporin antibiotic. Cefuracetime (SKF81367)  Chemical Structure
  17. GC18670 Cefuroxime Cefuroxime is an orally active second-generation cephalosporin antibiotic with increased stability to β-lactamase. Cefuroxime  Chemical Structure
  18. GC39548 Cefuroxime axetil Cefuroxime Axetil, a prodrug of the cephalosporin cefuroxime and an oarl broad spectrum antibiotic, inhibits several gram-positive and gram-negative organisms, including those most frequently associated with various common community-acquired infections. Cefuroxime axetil  Chemical Structure
  19. GC32086 Cefuroxime sodium (Cefuroxime sodium salt) Cefuroxime sodium (Cefuroxime sodium salt) is an orally active second-generation cephalosporin antibiotic with increased stability to β-lactamase. Cefuroxime sodium (Cefuroxime sodium salt)  Chemical Structure
  20. GC47069 Cefuroxime-d3 An internal standard for the quantification of cefuroxime Cefuroxime-d3  Chemical Structure
  21. GC14356 Celastramycin A inhibits the growth of bacteria and mycobacteria Celastramycin A  Chemical Structure
  22. GC32191 Celgosivir (MBI 3253)

    MBI 3253; MDL 28574; MX3253

    Celgosivir (MBI 3253) (MBI 3253; MDL 28574; MX3253) is an α-glucosidase I inhibitor; inhibits bovine viral diarrhoea virus (BVDV) with an IC50 of 1.27 μM in in vitro assay. Celgosivir (MBI 3253)  Chemical Structure
  23. GC32074 Celgosivir hydrochloride (MBI 3253 (hydrochloride))

    MBI 3253 hydrochloride; MDL 28574 hydrochloride; MX3253 hydrochloride

    Celgosivir hydrochloride (MBI 3253 (hydrochloride)) (MBI 3253 hydrochloride; MDL 28574 hydrochloride; MX3253 hydrochloride) is an α-glucosidase I inhibitor; inhibits bovine viral diarrhoea virus (BVDV) with an IC50 of 1.27 μM in in vitro assay. Celgosivir hydrochloride (MBI 3253 (hydrochloride))  Chemical Structure
  24. GC19101 Cenicriviroc

    TAK-652

    Cenicriviroc (CVC) is an oral, dual CCR2/CCR5 antagonist with nanomolar potency against both receptors. Cenicriviroc  Chemical Structure
  25. GC35650 Cenicriviroc Mesylate

    TAK-652 Mesylate; TBR-652 Mesylate

    Cenicriviroc Mesylate (TAK-652 Mesylate) is a dual CCR2/CCR5 antagonist, also inhibits both HIV-1 and HIV-2, and displays potent anti-inflammatory and antiinfective activity. Cenicriviroc Mesylate  Chemical Structure
  26. GC64261 Censavudine

    OBP-601; BMS-986001

    Censavudine (OBP-601; BMS-986001), a nucleoside analog, is a nucleoside reverse transcriptase inhibitor. Censavudine  Chemical Structure
  27. GC49593 Cephacetrile

    Cefacetrile, 7-Cyanoacetamidocephalosporanic Acid

    Cephacetrile (Cephacetrile) is a broad-spectrum antibiotic that is effective in gram-positive and gram-negative bacterial infection. Cephacetrile  Chemical Structure
  28. GC43228 Cephaeline

    (-)-Cephaeline

    Cephaeline is an alkaloid originally isolated from C. Cephaeline  Chemical Structure
  29. GC15625 Cephalexin

    Cefalexin

    Antibiotic Cephalexin  Chemical Structure
  30. GC13641 Cephalexin hydrochloride Cephalosporin antibiotic Cephalexin hydrochloride  Chemical Structure
  31. GC15593 Cephalexin monohydrate Semisynthetic cephalorsporin antibiotic Cephalexin monohydrate  Chemical Structure
  32. GC68853 Cephaloridine hydrate

    Cephaloridine hydrate is a broad-spectrum antibiotic. It has some dose-related kidney toxicity.

    Cephaloridine hydrate  Chemical Structure
  33. GC35653 Cephalotaxlen

    (–)-Cephalotaxine, NSC 128487, NSC 245454, ZINC19795976

    Cephalotaxlen ((-)-Cephalotaxlen) is an alkaloid that can be isolated from Cephalotaxus drupacea, with antileukemic and antiviral activities. Cephalotaxlen  Chemical Structure
  34. GC11507 Cephalothin NULL Cephalothin  Chemical Structure
  35. GC38664 Cephalothin sodium Cephalothin sodium is a first generation cephem antibiotic with a wide range antibacterial activity, is active against gram-positive and gram-negative bacteria. Cephalothin sodium  Chemical Structure
  36. GC19760 Cephapirin Benzathine Cephapirin Benzathine is the benzathine salt form of cephapirin. Cephapirin Benzathine  Chemical Structure
  37. GC38188 Cephapirin sodium Cephapirin sodium (Cefapirin sodium) is an ephalosporin antibiotic with broad-spectrum antimicrobial activity. Cephapirin sodium  Chemical Structure
  38. GN10113 Cepharanthine

    O-Methylcepharanoline, NSC 623442

    Cepharanthine  Chemical Structure
  39. GC25218 Cephradine monohydrate Cefradine is a beta-lactam, first-generation cephalosporin antibiotic with bactericidal activity. Cephradine monohydrate  Chemical Structure
  40. GC32323 Ceratotoxin A Ceratotoxin A, a 29-residue peptide isolated from the accessory gland secretion fluid, with strong anti-bacterial activity. Ceratotoxin A  Chemical Structure
  41. GC15391 Cercosporamide

    (-)-Cercosporamide

    A potent inhibitor of fungal Pkc1 and mammalian Mnk isoforms

    Cercosporamide  Chemical Structure
  42. GC65430 Cerebroside B Cerebroside B, a sphingolipid compound, is a non-racespecific elicitor, which elicits defense responses in rice. Cerebroside B  Chemical Structure
  43. GC60689 Cetalkonium chloride Cetalkonium chloride is an ammonium antiseptic agent used in many topical drugs for infections of mouth, throat and eye. Cetalkonium chloride  Chemical Structure
  44. GC65087 Cethromycin Cethromycin (ABT-773) is a ketolide antibiotic. Cethromycin  Chemical Structure
  45. GC11689 Cetylpyridinium Chloride

    Hexadecylpyridinium

    Cationic quaternary ammonium compound used as oropharyngeal antiseptic.

    Cetylpyridinium Chloride  Chemical Structure
  46. GC35658 Cetylpyridinium chloride monohydrate Cetylpyridinium chloride monohydrate is a cationic quaternary ammonium compound, used in some types of mouthwashes, toothpastes, throat and nasal sprays, is an antiseptic that kills bacteria and other microorganisms, effective in preventing dental plaque and reducing gingivitis. Cetylpyridinium chloride monohydrate  Chemical Structure
  47. GC63826 Chalcone Chalcone is isolated from Glycyrrhizae inflata and used to synthesize chalcone derivatives. Chalcone  Chemical Structure
  48. GC70407 Chalcone 4 hydrate Chalcone 4 hydrate is an anti-parasite agent, inhibits the growth of Babesia and Theileria. Chalcone 4 hydrate  Chemical Structure
  49. GC68859 Chamaechromone

    Chamaechromone is a flavonoid component isolated from the roots of plants in the thyme family. It has anti-hepatitis B virus (HBV) activity, inhibits the surface secretion antigen (HBsAg) of hepatitis B virus, and also has insecticidal activity.

    Chamaechromone  Chemical Structure
  50. GC31707 Chebulagic acid Chebulagic acid is a COX-LOX dual inhibitor isolated from the fruits of Terminalia chebula Retz, on angiogenesis. Chebulagic acid  Chemical Structure
  51. GC14386 CHIR-090

    CHIR 090;CHIR090

    An antibiotic and LpxC inhibitor CHIR-090  Chemical Structure
  52. GC68860 Chitin synthase inhibitor 4

    Chitin synthase inhibitor 4 (compound 4fh) is a chitin synthase (CHS) inhibitor with fungicidal properties. Chitin synthase inhibitor 4 is a potential CHS-based agricultural fungicide.

    Chitin synthase inhibitor 4  Chemical Structure
  53. GC72154 Chitinase, serratia marcescens Chitinase (EC 3.2.1.14) has partial lysozyme activity and is widely found in bacteria, fungi, animals and some plants. Chitinase, serratia marcescens  Chemical Structure
  54. GC35676 Chitinase-IN-1 Chitinase-IN-1 is a insect chitinase and N- acetyl hexosaminidase inhibitor and pesticide; 50 uM/20 uM compound concentration's inhibitory percentage are 75%/67% for chitinase/N- acetyl-hexosaminidase respectively. Chitinase-IN-1  Chemical Structure
  55. GC34082 Chitosan (Deacetylated chitin) Chitosan (Deacetylated chitin) (Deacetylated chitin) is a polycationic linear polysaccharide derived from chitin. Chitosan (Deacetylated chitin)  Chemical Structure
  56. GC47079 Chloramine-T (hydrate) A common reagent Chloramine-T (hydrate)  Chemical Structure
  57. GC15185 Chloramphenicol Chloramphenicol is a highly lipid-soluble broad-spectrum antibiotic for bacterial infections. Chloramphenicol inhibits protein synthesis by binding to the 50S subunit of the ribosome, thus acting as an antibacterial agent. Chloramphenicol can be used in the treatment of meningitis and cancer research. Chloramphenicol  Chemical Structure
  58. GC43241 Chloramphenicol Palmitate Chloramphenicol palmitate is an orally bioavailable ester prodrug form of the antibiotic chloramphenicol. Chloramphenicol Palmitate  Chemical Structure
  59. GC43242 Chloramphenicol Succinate Chloramphenicol succinate is a water-soluble prodrug form of the antibiotic chloramphenicol. Chloramphenicol Succinate  Chemical Structure
  60. GC39661 Chloramphenicol succinate sodium Chloramphenicol succinate sodium is a prodrug of Chloramphenicol, with Haemotoxicity. Chloramphenicol succinate sodium  Chemical Structure
  61. GC71628 Chloramphenicol-d5 Chloramphenicol-d5 is the deuterium labeled Chloramphenicol. Chloramphenicol-d5  Chemical Structure
  62. GC32394 Chlordantoin (Clodantoin) Chlordantoin (Clodantoin) is an antifungal agent and has the potential for vaginal candidiasis treatment. Chlordantoin (Clodantoin)  Chemical Structure
  63. GC35680 Chlorhexidine Chlorhexidine is an antibacterial used as an antiseptic and for other applications. Chlorhexidine  Chemical Structure
  64. GC43243 Chlorhexidine (acetate hydrate)

    CHX

    Chlorhexidine is a bis(biguanide) antimicrobial disinfectant and antiseptic agent. Chlorhexidine (acetate hydrate)  Chemical Structure
  65. GC60699 Chlorhexidine diacetate Chlorhexidine diacetate is a biguanide disinfectant with rapid bactericidal activity against both Gram-positive and Gram-negative organism. Chlorhexidine diacetate  Chemical Structure
  66. GC16201 Chlorhexidine digluconate antiseptic Chlorhexidine digluconate  Chemical Structure
  67. GC15204 Chlorhexidine HCl

    CHX

    Chlorhexidine HCl is an antibacterial, used as an antiseptic and for other applications. Chlorhexidine HCl  Chemical Structure
  68. GC39601 Chlormidazole hydrochloride

    Clomidazole hydrochloride

    Chlormidazole hydrochloride is an antifungal agent and has inhibitory activity against many fungi and some gram-positive cocci. Chlormidazole hydrochloride  Chemical Structure
  69. GC39358 Chlorobutanol Chlorobutanol is a pharmaceutical preservative. Chlorobutanol  Chemical Structure
  70. GC62358 Chlorobutanol hemihydrate Chlorobutanol hemihydrate is a pharmaceutical preservative. Chlorobutanol hemihydrate  Chemical Structure
  71. GC19549 Chloroquine

    CHLORO QUINE PHOSPHATE; 4-(7-chloro-4-quinolylamino)pentyldiethylamine; (4S)-N~4~-(7-chloroquinolin-4-yl)-N~1~,N~1~-diethylpentane-1,4-diamine

    An autophagy and toll-like receptors (TLRs) inhibitor

    Chloroquine  Chemical Structure
  72. GC60700 Chloroquine D5 Chloroquine D5 is deuterium labeled Chloroquine. Chloroquine D5  Chemical Structure
  73. GC10295 Chloroquine diphosphate

    DL-Chloroquine, NSC 14050

    Chloroquine diphosphate is an antimalarial and anti-inflammatory agent widely used to treat malaria and rheumatoid arthritis. Chloroquine diphosphate  Chemical Structure
  74. GC45885 Chloroquine-d5 (phosphate)

    DL-Chloroquine-d5

    An internal standard for the quantification of chloroquine Chloroquine-d5 (phosphate)  Chemical Structure
  75. GC60107 Chloroquinoxaline sulfonamide Chloroquinoxaline sulfonamide (Chloroquinoxaline), a structural analogue of sulfaquinoxaline, is a topoisomerase II alpha/beta poison. Chloroquinoxaline sulfonamide  Chemical Structure
  76. GC47082 Chlorothalonil

    2,4,5,6-Tetrachloroisophthalonitrile

    A broad-spectrum organochlorine fungicide Chlorothalonil  Chemical Structure
  77. GC16628 Chlorothricin

    Antibiotic K 818A

    macrolide-type antibiotic Chlorothricin  Chemical Structure
  78. GC17165 Chloroxine synthetic antibacterial compound Chloroxine  Chemical Structure
  79. GC33937 Chloroxylenol (4-Chloro-3,5-dimethylphenol) Chloroxylenol (4-Chloro-3,5-dimethylphenol) is a broad spectrum antimicrobial chemical compound used to control bacteria, algae, fungi and virus. Chloroxylenol (4-Chloro-3,5-dimethylphenol)  Chemical Structure
  80. GC71694 Chloroxylenol-d6 Chloroxylenol-d6 is the deuterium labeled Chloroxylenol. Chloroxylenol-d6  Chemical Structure
  81. GC60701 Chlorphenesin

    (±)-p-Chlorphenesin, NSC 6401

    Chlorphenesin is a reversible antigen-associated immunosuppressant. Chlorphenesin  Chemical Structure
  82. GC15312 Chlorprothixene Dopamine receptor antagonist Chlorprothixene  Chemical Structure
  83. GC17540 Chlorquinaldol Antifungal and antibacterial Chlorquinaldol  Chemical Structure
  84. GC40996 Chlortetracycline

    7-Chlortetracycline

    Chlortetracycline is a broad-spectrum antibiotic originally isolated from S. Chlortetracycline  Chemical Structure
  85. GC60702 Chlortetracycline hydrochloride Chlortetracycline hydrochloride (7-Chlorotetracycline hydrochloride) is a specific and potent calcium ionophore antibiotic, inhibits binding of aminoacyl-tRNA to ribosomes. Chlortetracycline hydrochloride  Chemical Structure
  86. GC43259 Cholesteryl Homo-γ-Linolenate

    20:3 (8Z,11Z,14Z) CE, 20:3 n-6 CE, 20:3 (8Z,11Z,14Z) Cholesterol Ester

    Cholesteryl homo-γ-linolenate is a cholesterol ester. Cholesteryl Homo-γ-Linolenate  Chemical Structure
  87. GC46119 Cholic Acid anilide A synthetic bile acid Cholic Acid anilide  Chemical Structure
  88. GC18344 Chrysomycin B

    Albacarcin M, Virenomycin M

    Chrysomycin B is an antibiotic isolated from a strain of Streptomyces. Chrysomycin B  Chemical Structure
  89. GC72052 Chrysophanol tetraglucoside Chrysophanol tetraglucoside possesses anti-hypolipidemic and antibacterial activities. Chrysophanol tetraglucoside  Chemical Structure
  90. GC64289 Cichoriin Cichoriin is an active compounds against SARS-CoV-2, and may be a potential candidate in treating severe COVID-19. Cichoriin  Chemical Structure
  91. GC10132 Ciclopirox

    HOE 296b

    broad-spectrum antifungal agent Ciclopirox  Chemical Structure
  92. GC11120 Ciclopirox ethanolamine Ciclopirox ethanolamine (Ciclopirox ethanolamine) is a synthetic antifungal agent that can be used for superficial mycoses reseaech. Ciclopirox ethanolamine  Chemical Structure
  93. GC25249 CID-1517823

    ML328

    CID-1517823 (ML328) is a potent and selective inhibitor of bacterial AddAB and RecBCD helicase-nucleases, with IC50s of 1.0 and 4.8 μM. CID-1517823  Chemical Structure
  94. GC12666 Cidofovir

    GS-0504, (S)-HPMPC, (S)-1-(3-hydroxy-2-phosphonylmethoxypropyl)cytosine

    Anti-CMV drug;inhibitor of viral DNA syntheis Cidofovir  Chemical Structure
  95. GC13936 Cidofovir dihydrate Antiviral agent for CMV Cidofovir dihydrate  Chemical Structure
  96. GC32162 Cilastatin (MK0791) Cilastatin (MK0791) (MK0791) is a reversible, competitive renal dehydropeptidase I inhibitor with an IC50 of 0.1 μM. Cilastatin (MK0791)  Chemical Structure
  97. GC72412 Cilgavimab Cilgavimab (AZD-1061; COV2-2130) is a human SARS-CoV-2-neutralizing monoclonal antibody, can compose monoclonal-antibody combination AZD7442 with Tixagevimab . Cilgavimab  Chemical Structure
  98. GC11840 Ciluprevir (BILN-2061)

    BILN 2061; BILN 2061ZW

    Inhibitor of HCV NS3 protease Ciluprevir (BILN-2061)  Chemical Structure
  99. GC16135 Cinanserin hydrochloride

    SQ 10,643

    5-HT2 antagonist Cinanserin hydrochloride  Chemical Structure
  100. GC11798 Cinchonidine alkaloid Cinchonidine  Chemical Structure
  101. GC32997 Cinchonine ((8R,9S)-Cinchonine) Cinchonine ((8R,9S)-Cinchonine) is a natural compound present in Cinchona bark. Cinchonine ((8R,9S)-Cinchonine) activates endoplasmic reticulum stress-induced apoptosis in human liver cancer cells. Cinchonine ((8R,9S)-Cinchonine)  Chemical Structure

Items 801 to 900 of 3275 total

per page

Set Descending Direction