Drug

D1296 | Ampicillin

Molecular Formula C16H19N3O4S
Molecular Weight 349.4
Structure
State solid
Route of elimination Ampicillin is excreted largely unchanged in the urine.
Description Antibiotic

S

J

S01AA19 Ampicillin


[S01AA] Antibiotics


[S01A] ANTIINFECTIVES


[S01] OPHTHALMOLOGICALS


[S] Sensory organs


J01CR50 Combinations of penicillins


[J01CR] Combinations of penicillins, incl. beta-lactamase inhibitors


[J01C] BETA-LACTAM ANTIBACTERIALS, PENICILLINS


[J01] ANTIBACTERIALS FOR SYSTEMIC USE


[J] Antiinfectives for systemic use


J01CA51 Ampicillin, combinations


[J01CA] Penicillins with extended spectrum


[J01C] BETA-LACTAM ANTIBACTERIALS, PENICILLINS


[J01] ANTIBACTERIALS FOR SYSTEMIC USE


[J] Antiinfectives for systemic use


J01CA01 Ampicillin


[J01CA] Penicillins with extended spectrum


[J01C] BETA-LACTAM ANTIBACTERIALS, PENICILLINS


[J01] ANTIBACTERIALS FOR SYSTEMIC USE


[J] Antiinfectives for systemic use


Toxicity Dose Time Species Model Method Action Positive criterion Reference
MEMBRANE POTENTIAL > 400 µM 30 mins mouse liver mitochondria Rh123 fluorescence (excitation 485 nm, emission 535 nm) are recorded using a fluorescence multi-well plate reader (mCICCP (20 µM) treatments was considered as the 100% baseline for ΔΨm loss) decrease EC20 36
RESPIRATION > 400 µM 60 mins mouse liver mitochondria Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. decrease EC20 36
RESPIRATION 161.2 µM 60 mins mouse liver mitochondria Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. increase EC20 36
SWELLING > 400 µM 30 mins mouse liver mitochondria swelling assay: Absorbance at 545 nm using a fluorescence multi-well plate reader (CaCl2 (50 µM) was considered as the 100% baseline for the swelling ) increase EC20 36

Target Dose Time Species Model Method Action Positive criterion Reference
NADH:ubiquinone reductase > 400 µM 60 mins mouse liver mitochondria Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. inhibit EC20 36
Cytochrome c > 400 µM 30 mins mouse liver mitochondria Cytochrome c release was evaluated using ELISA kit ( 20 µg/ml Alamethicin was used as 100% baseline) release EC20 36

Pictogram Signal Statements Precautionary Statement Codes
Danger

Aggregated GHS information provided by 310 companies from 10 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.


Reported as not meeting GHS hazard criteria by 1 of 310 companies. For more detailed information, please visit ECHA C&L website


Of the 9 notification(s) provided by 309 of 310 companies with hazard statement code(s):


H317 (99.35%): May cause an allergic skin reaction [Warning Sensitization, Skin]


H334 (99.68%): 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.)
Danger

Aggregated GHS information provided by 261 companies from 8 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.


Reported as not meeting GHS hazard criteria by 1 of 261 companies. For more detailed information, please visit ECHA C&L website


Of the 7 notification(s) provided by 260 of 261 companies with hazard statement code(s):


H315 (15.77%): Causes skin irritation [Warning Skin corrosion/irritation]


H317 (98.85%): May cause an allergic skin reaction [Warning Sensitization, Skin]


H319 (15.77%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]


H334 (99.62%): May cause allergy or asthma symptoms or breathing difficulties if inhaled [Danger Sensitization, respiratory]


H335 (15.77%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure


Respiratory tract irritation]


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, P264, P271, P272, P280, P285, P302+P352, P304+P340, P304+P341, P305+P351+P338, P312, P321, P332+P313, P333+P313, P337+P313, P342+P311, P362, P363, P403+P233, P405, and P501; (The corresponding statement to each P-code can be found at the GHS Classification page.)
Danger

Aggregated GHS information provided by 1426 companies from 12 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.


H315 (97.41%): Causes skin irritation [Warning Skin corrosion/irritation]


H317 (98.04%): May cause an allergic skin reaction [Warning Sensitization, Skin]


H319 (97.41%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]


H334 (99.93%): May cause allergy or asthma symptoms or breathing difficulties if inhaled [Danger Sensitization, respiratory]


H335 (97.34%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure


Respiratory tract irritation]


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, P264, P271, P272, P280, P285, P302+P352, P304+P340, P304+P341, P305+P351+P338, P312, P321, P332+P313, P333+P313, P337+P313, P342+P311, P362, P363, P403+P233, P405, 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
mouse LD50 intracrebral 380mg/kg (380mg/kg) Chemotherapy Vol. 26, Pg. 196, 1980.
cat LDLo intravenous > 100mg/kg (100mg/kg) British Medical Journal. Vol. 2, Pg. 197, 1961.
rat LDLo subcutaneous > 5gm/kg (5000mg/kg) British Medical Journal. Vol. 2, Pg. 197, 1961.
guinea pig LD50 unreported 7500ug/kg (7.5mg/kg) Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 42(9), Pg. 10, 1977.
rat LD50 intravenous 6200mg/kg (6200mg/kg) Drugs in Japan Vol. -, Pg. 88, 1990.
rat LDLo oral > 5gm/kg (5000mg/kg) British Medical Journal. Vol. 2, Pg. 197, 1961.
mouse LD50 intravenous 4600mg/kg (4600mg/kg) Yakugaku Zasshi. Journal of Pharmacy. Vol. 97, Pg. 987, 1977.
mouse LD50 parenteral > 3gm/kg (3000mg/kg) Drugs in Japan Vol. -, Pg. 114, 1995.
mouse LD50 oral > 5gm/kg (5000mg/kg) Drugs in Japan Vol. 6, Pg. 57, 1982.
mouse LD50 unreported 28gm/kg (28000mg/kg) Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 42(9), Pg. 10, 1977.
mouse LD50 intraperitoneal 3250mg/kg (3250mg/kg) Eksperimental'naya i Klinicheskaya Farmakoterapiya. Vol. 9, Pg. 83, 1980.
rat LD50 intraperitoneal 4500mg/kg (4500mg/kg) Toxicology and Applied Pharmacology. Vol. 18, Pg. 185, 1971.
mouse LDLo subcutaneous > 5gm/kg (5000mg/kg) British Medical Journal. Vol. 2, Pg. 197, 1961.
rat LD50 parenteral > 3gm/kg (3000mg/kg) Drugs in Japan Vol. -, Pg. 114, 1995.
rat LD50 unreported 10gm/kg (10000mg/kg) Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 42(9), Pg. 10, 1977.
women TDLo oral 160mg/kg/4D-I (160mg/kg) Annals of Internal Medicine. Vol. 99, Pg. 573, 1983.
man TDLo oral 400mg/kg/4W-I (400mg/kg) Annals of Internal Medicine. Vol. 69, Pg. 91, 1968.


  • DrugBank DB00415
    CAS Number 33276-75-4, 69-52-3, 69-53-4, 7177-48-2, 800-79-3
    PubChem Compound 6249