Products 145435-72-9

CAS 145435-72-9 appears in our catalog under these names: Gamithromycin, 95%, Gamithromycin, Gamithromycin, >95% (HPLC), Gamithromycin 100 µg/mL in Methanol, Gamithromycin/ 99.55% (existing batch purity). Offered by: Combi-blocks, Chemat Brand, TRC, Dr. Ehrenstorfer, TargetMol. Available pack sizes: 250mg, 1g, 5g, on request, 10mg, 1mg, 2,5mg, 50mg.

Gamithromycin, 95%
Combi-blocks
  • size: 250mg, 1g, 5g
  • Variants: 3
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Gamithromycin
Chemat Brand, Dr. Ehrenstorfer, Biosynth
  • size: on request, 50mg, 2g, 5g
  • Variants: 9
from 840.05
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Gamithromycin, >95% (HPLC)
TRC
  • size: 10mg, 1mg, 2,5mg
  • Variants: 3
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Gamithromycin 100 µg/mL in Methanol
Dr. Ehrenstorfer
  • size: 1ml
  • Variants: 1
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Gamithromycin/ 99.55% (existing batch purity)
TargetMol
  • size: 5mg, 10mg, 25mg, 50mg
  • Variants: 6
from 405.71
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Gamithromycin (ML–1709460)
GLPBio
  • size: 10mg, 100mg, 25mg, 5mg
  • Variants: 6
from 676.61
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Gamithromycin, 95.00%
Chemat
  • size: 25mg
  • Variants: 1
from 548.83
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Gamithromycin 95%
Ambeed
  • size: 1mg, 5mg, 10mg, 50mg
  • Variants: 8
from 125.62
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Gamithromycin, 95%, 95%
Chemat
  • size: 10mg, 50mg, 100mg, 250mg
  • Variants: 8
from 83.60
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Gamithromycin, 99.95%
MedChemExpress
  • size: 25 mg, 50 mg, 100 mg, 5 mg
  • Variants: 6
from 519.38
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Gamithromycin (Standard)
MedChemExpress
  • size: 100 mg, 25 mg, 5 mg, 10 mg
  • Variants: 5
from 719.08
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Gamithromycin, min. 95 %, 2 g
Roth
  • size: 2g
  • Variants: 1
from 844.81
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Gamithromycin, min. 95 %, 5 g
Roth
  • size: 5g
  • Variants: 1
from 1505.56
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Gamithromycin, min. 95 %, 10 g
Roth
  • size: 10g
  • Variants: 1
from 2213.50
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Gamithromycin, min. 95 %, 25 g
Roth
  • size: 25g
  • Variants: 1
from 3516.11
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Structural formula: {0} (CAS {1})

Gamithromycin is a macrolide antibiotic with formula C40H76N2O12. It is used for the treatment of of bovine respiratory disease caused by Mannheimia haemolytica, Pasteurella multocida, Histophilus somni and Mycoplasma bovis in beef and non-lactating dairy cattle. The compound is also licensed in Europe for the treatment of footrot in sheep caused by Dichelobacter nodosus and Fusobacterium nodosus. It has a role as an antibacterial drug and a protein synthesis inhibitor. It is a macrolide antibiotic and a monosaccharide derivative.

Source: ChEBI

Identity
Molecular formulaC40H76N2O12
Molecular weight777.0 g/mol
IUPAC name(2R,3S,4R,5S,8R,10R,11R,12S,13S,14R)-11-[(2S,3R,4S,6R)-4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy-2-ethyl-3,4,10-trihydroxy-13-[(2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyloxan-2-yl]oxy-3,5,8,10,12,14-hexamethyl-7-propyl-1-oxa-7-azacyclopentadecan-15-one
InChIKeyVWAMTBXLZPEDQO-UZSBJOJWSA-N
SMILESCCCN1C[C@@H]([C@H]([C@]([C@H](OC(=O)[C@@H]([C@H]([C@@H]([C@H]([C@](C[C@H]1C)(C)O)O[C@H]2[C@@H]([C@H](C[C@H](O2)C)N(C)C)O)C)O[C@H]3C[C@@]([C@H]([C@@H](O3)C)O)(C)OC)C)CC)(C)O)O)C

Computed by PubChem (NCBI)

Synonyms: Gamithromycin, gamitromicina, gamithromycinum, Zactran, Gamithromycin [USAN:INN], Zactran (veterinary), GAMITHROMYCIN [MI], GAMITHROMYCIN [INN], GAMITHROMYCIN [USAN], orb1226238