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Details

Stereochemistry ABSOLUTE
Molecular Formula C42H64N2.2C16H18N2O5S
Molecular Weight 1297.75
Optical Activity UNSPECIFIED
Defined Stereocenters 12 / 12
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PENICILLIN V HYDRABAMINE

SMILES

[H][C@]12SC(C)(C)[C@@H](N1C(=O)[C@H]2NC(=O)COC3=CC=CC=C3)C(O)=O.[H][C@]45SC(C)(C)[C@@H](N4C(=O)[C@H]5NC(=O)COC6=CC=CC=C6)C(O)=O.[H][C@@]78CCC9=C(C=CC(=C9)C(C)C)[C@@]7(C)CCC[C@@]8(C)CNCCNC[C@]%10(C)CCC[C@]%11(C)C%12=C(CC[C@@]%10%11[H])C=C(C=C%12)C(C)C

InChI

InChIKey=IJXFBPWHGGIUAV-YQUITFMISA-N
InChI=1S/C42H64N2.2C16H18N2O5S/c1-29(2)31-11-15-35-33(25-31)13-17-37-39(5,19-9-21-41(35,37)7)27-43-23-24-44-28-40(6)20-10-22-42(8)36-16-12-32(30(3)4)26-34(36)14-18-38(40)42;2*1-16(2)12(15(21)22)18-13(20)11(14(18)24-16)17-10(19)8-23-9-6-4-3-5-7-9/h11-12,15-16,25-26,29-30,37-38,43-44H,9-10,13-14,17-24,27-28H2,1-8H3;2*3-7,11-12,14H,8H2,1-2H3,(H,17,19)(H,21,22)/t37-,38-,39-,40-,41+,42+;2*11-,12+,14-/m011/s1

HIDE SMILES / InChI
PENICILLIN V HYDRABAMINE, a semi-synthetic antibiotic, is used for the treatment of mild to moderately severe infections (e.g. dental infection, infections in the heart, middle ear infections, rheumatic fever, scarlet fever, skin infections, upper and lower respiratory tract infections) caused by susceptible, usually gram-positive, organisms.

Approval Year

Conditions
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
5.73 μg/mL
500 mg single, oral
dose: 500 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
PENICILLIN V plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE
food status: FASTED
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
8.23 μg × h/mL
500 mg single, oral
dose: 500 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
PENICILLIN V plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE
food status: FASTED
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
2 h
500 mg single, oral
dose: 500 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
PENICILLIN V plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE
food status: FASTED
Funbound

Funbound

ValueDoseCo-administeredAnalytePopulation
20%
500 mg single, oral
dose: 500 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
PENICILLIN V plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE
food status: FASTED
PubMed

PubMed

TitleDatePubMed
Penicillin V blood levels after oral administration of the benzathine and hydrabamine salts.
1960 Oct 8
Name Type Language
PENICILLIN V HYDRABAMINE
MI   USAN  
USAN  
Official Name English
ABBOCILLIN V
Common Name English
COMPOCILLIN V HYDRABAMINE
Common Name English
PENICILLIN V HYDRABAMINE [USAN]
Common Name English
COMPOCILLIN V
Common Name English
PHENOXYMETHYLPENICILLIN HYDRABAMINE
WHO-DD  
Common Name English
HYDRABAMINE PHENOXYMETHYLPENICILLIN
MART.  
Common Name English
PENICILLIN PHENOXYMETHYL HYDRABAMINE
Common Name English
HYDRABAMINE PHENOXYMETHYLPENICILLIN [MART.]
Common Name English
Phenoxymethylpenicillin hydrabamine [WHO-DD]
Common Name English
HYDRABAMINE PENICILLIN V
Common Name English
PENICILLIN HYDRABAMINE PHENOXYMETHYL
Common Name English
PENICILLIN V HYDRABAMINE [MI]
Common Name English
Code System Code Type Description
PUBCHEM
23724984
Created by admin on Fri Dec 15 15:26:34 GMT 2023 , Edited by admin on Fri Dec 15 15:26:34 GMT 2023
PRIMARY
MERCK INDEX
m387
Created by admin on Fri Dec 15 15:26:34 GMT 2023 , Edited by admin on Fri Dec 15 15:26:34 GMT 2023
PRIMARY Merck Index
CAS
6591-72-6
Created by admin on Fri Dec 15 15:26:34 GMT 2023 , Edited by admin on Fri Dec 15 15:26:34 GMT 2023
PRIMARY
FDA UNII
8T7T79P87L
Created by admin on Fri Dec 15 15:26:34 GMT 2023 , Edited by admin on Fri Dec 15 15:26:34 GMT 2023
PRIMARY
NCI_THESAURUS
C175188
Created by admin on Fri Dec 15 15:26:34 GMT 2023 , Edited by admin on Fri Dec 15 15:26:34 GMT 2023
PRIMARY
SMS_ID
100000085295
Created by admin on Fri Dec 15 15:26:34 GMT 2023 , Edited by admin on Fri Dec 15 15:26:34 GMT 2023
PRIMARY
EVMPD
SUB03765MIG
Created by admin on Fri Dec 15 15:26:34 GMT 2023 , Edited by admin on Fri Dec 15 15:26:34 GMT 2023
PRIMARY
CHEBI
52173
Created by admin on Fri Dec 15 15:26:34 GMT 2023 , Edited by admin on Fri Dec 15 15:26:34 GMT 2023
PRIMARY