Drug

D0020 | Cephaloglycin

Molecular Formula C18H19N3O6S
Molecular Weight 405.4
Structure
State solid
Absorption Well absorbed following oral administration.
Description cephalorsporin antibiotic; Antibacterial

Toxicity Dose Time Species Model Method Action Positive criterion Reference
RESPIRATION inhibit 197

Pictogram Signal Statements Precautionary Statement Codes
Danger

Aggregated GHS information provided by 38 companies from 1 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.


H317 (100%): May cause an allergic skin reaction [Warning Sensitization, Skin]


H334 (100%): May cause allergy or asthma symptoms or breathing difficulties if inhaled [Danger Sensitization, respiratory]


Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown.


P261, P272, P280, P285, P302+P352, P304+P341, P321, P333+P313, P342+P311, P363, and P501; (The corresponding statement to each P-code can be found at the GHS Classification page.)

Organism Test type Route Dose (normalized dose) Effect Source
rat LD50 subcutaneous 2800mg/kg (2800mg/kg) kidney, ureter, and bladder: "changes in tubules (including acute renal failure, acute tubular necrosis)" Chemotherapy Vol. 18, Pg. 22, 1970.
rat LD50 intraperitoneal 1300mg/kg (1300mg/kg) kidney, ureter, and bladder: "changes in tubules (including acute renal failure, acute tubular necrosis)" Chemotherapy Vol. 18, Pg. 22, 1970.
rat LD50 oral > 10gm/kg (10000mg/kg) liver: other changes Chemotherapy Vol. 18, Pg. 22, 1970.
mouse LD50 subcutaneous 3700mg/kg (3700mg/kg) kidney, ureter, and bladder: "changes in tubules (including acute renal failure, acute tubular necrosis)" Chemotherapy Vol. 18, Pg. 22, 1970.
mouse LD50 intraperitoneal 1030mg/kg (1030mg/kg) kidney, ureter, and bladder: "changes in tubules (including acute renal failure, acute tubular necrosis)" Chemotherapy Vol. 18, Pg. 22, 1970.
mouse LD50 oral > 10gm/kg (10000mg/kg) liver: other changes Chemotherapy Vol. 18, Pg. 22, 1970.


  • (6R,7R)-3-(acetoxymethyl)-7-{[(2R)-2-amino-2-phenylacetyl]amino}-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid (6R,7R)-3-[(acetyloxy)methyl]-7-[(2R)-2-amino-2-phenylacetamido]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid (6R,7R)-3-[(acetyloxy)methyl]-7-{[(2R)-2-amino-2-phenylacetyl]amino}-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
    3-((Acetyloxy)methyl)-7-((aminophenylacetyl)amino)-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid 3-acetoxymethyl-7beta-[(2R)-2-amino-2-phenylacetamido]-3,4-didehydrocepham-4-carboxylic acid 3577-01-3
    5-Thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid, 3-((acetyloxy)methyl)-7-((aminophenylacetyl)amino)-8-oxo-, (6R-(6alpha,7beta(R*)))- 5-Thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid, 7-(2-amino-2-phenylacetamido)-3-(hydroxymethyl)-8-oxo-, acetate (ester), D- 7-(2-Amino-2-phenylacetamido)-3-(hydroxymethyl)-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid acetate (ester)
    7-(2-Amino-2-phenylacetamido)-3-(hydroxymethyl)-8-oxo-5-thia-1-azabicyclo(4.2.0)octane-2-carboxylic acid, acetate inner salt 7-(2-D-alpha-Aminophenylacetamido)cephalosporanic acid 7-(D-2-Amino-2-phenylacetamido)-3-acetoxymethyl-delta(sup 3)-cephem-4-carboxylic acid
    7-(D-2-Amino-2-phenylacetamido)-3-acetoxymethyl-delta(sup3)-cephem-4-carboxylic acid 7-(D-alpha-Aminophenyl-acetamido)cephalosporanic acid API0001931
    C13440 C18H19N3O6S CEG
    CEPHALOGLYCIN CHEBI:34613 CHEMBL1200971
    Cefaloglicina Cefaloglicina [INN-Spanish] Cefaloglycin
    Cefaloglycin (JAN) Cefaloglycin [INN] Cefaloglycine
    Cefaloglycine [INN-French] Cefaloglycinum Cefaloglycinum [INN-Latin]
    Cephaloglycin (anhydrous) Cephaloglycin anhdyous Cephaloglycin anhydrous
    Cephaloglycine Cephaoglycin acid D-(-)-Cephaloglycin
    D-Cephaloglycine D01949 DB00689
    DTXSID4022781 EINECS 222-696-7 Epitope ID:174844
    FUBBGQLTSCSAON-PBFPGSCMSA-N HD2D469W6U HSDB 3214
    Kafocin Kefglycin LS-149962
    Lilly 39435 Q5057214 SCHEMBL2947
    UNII-HD2D469W6U ZINC3830503

    DrugBank Name Cephaloglycin
    DrugBank DB00689
    CAS Number 3577-01-03 00:00:00
    PubChem Compound 19150
    KEGG Compound ID C13440
    KEGG Drug D01949
    PubChem.Substance 46506850
    ChEBI 34613
    PharmGKB PA164781027
    ChemSpider 18069
    TTD DAP001158
    Wikipedia Cephaloglycin

    1. Vuda et al. (2016)