PENICILLIN G

U.S. Department of Health & Human Services Divider Arrow

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C16H18N2O4S
Molecular Weight	334.39
Optical Activity	UNSPECIFIED
Defined Stereocenters	3 / 3
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of PENICILLIN G

Structure Search

SMILES

[H][C@]12SC(C)(C)[C@@H](N1C(=O)[C@H]2NC(=O)CC3=CC=CC=C3)C(O)=O

InChI

InChIKey=JGSARLDLIJGVTE-MBNYWOFBSA-N

InChI=1S/C16H18N2O4S/c1-16(2)12(15(21)22)18-13(20)11(14(18)23-16)17-10(19)8-9-6-4-3-5-7-9/h3-7,11-12,14H,8H2,1-2H3,(H,17,19)(H,21,22)/t11-,12+,14-/m1/s1

HIDE SMILES / InChI

Molecular Formula	C16H18N2O4S
Molecular Weight	334.39
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	3 / 3
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

Substance Class	Chemical Created by `admin` on `Fri Dec 15 14:58:04 UTC 2023` Edited by `admin` on `Fri Dec 15 14:58:04 UTC 2023`
Record UNII	Q42T66VG0C
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

PENICILLIN G

Common Name

English

benzylpenicillin [INN]

Common Name

English

Benzylpenicillin [WHO-DD]

Common Name

English

PENICILLIN G [MI]

Common Name

English

(2S,5R,6R)-3,3-DIMETHYL-7-OXO-6-(2-PHENYLACETAMIDO)-4-THIA-1-AZABICYCLO(3.2.0)HEPTANE-2-CARBOXYLIC ACID

Systematic Name

English

PENICILLIN G [VANDF]

Common Name

English

J01CE01

Code

English

BENZYLPENICILLIN

Official Name

English

NSC-193396

Code

English

BENZYL PENICILLIN

Common Name

English

PHENOXYMETHYLPENICILLIN POTASSIUM IMPURITY A [EP IMPURITY]

Common Name

English

PHENOXYMETHYLPENICILLIN (BENZATHINE) TETRAHYDRATE IMPURITY A [EP IMPURITY]

Common Name

English

PENICILLIN G [HSDB]

Common Name

English

PHENOXYMETHYLPENICILLIN IMPURITY A [EP IMPURITY]

Common Name

English

BENZYLPENICILLIN [MART.]

Common Name

English

Classification Tree Code System Code

NDF-RT

N0000011281

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

NDF-RT

N0000011281

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

NCI_THESAURUS

C1500

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

NDF-RT

N0000011281

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

LIVERTOX

NBK547993

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

FDA ORPHAN DRUG

37689

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

WHO-ATC

J01CE01

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

WHO-VATC

QS01AA14

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

WHO-ATC

J01CE09

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

WHO-VATC

QJ51CE01

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

CFR

21 CFR 520.1696B

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

NDF-RT

N0000011281

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

NDF-RT

N0000175497

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

WHO-VATC

QJ01CE01

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

FDA ORPHAN DRUG

18787

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

WHO-VATC

QJ51RC22

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

NDF-RT

N0000011281

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

NDF-RT

N0000011281

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

NDF-RT

N0000011281

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

WHO-ESSENTIAL MEDICINES LIST

6.2.1

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

NDF-RT

N0000011281

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

WHO-ATC

S01AA14

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

NDF-RT

N0000011281

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

WHO-VATC

QG51AG02

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

Code System Code Type Description

DAILYMED

Q42T66VG0C

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

PRIMARY

ChEMBL

CHEMBL29

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

PRIMARY

ECHA (EC/EINECS)

200-506-3

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

PRIMARY

MESH

D010400

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

PRIMARY

DRUG CENTRAL

2082

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

PRIMARY

CAS

61-33-6

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

PRIMARY

FDA UNII

Q42T66VG0C

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

PRIMARY

NSC

193396

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

PRIMARY

SMS_ID

100000091070

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

PRIMARY

WIKIPEDIA

BENZYLPENICILLIN

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

PRIMARY

IUPHAR

4796

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

PRIMARY

NCI_THESAURUS

C61883

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

PRIMARY

EVMPD

SUB05772MIG

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

PRIMARY

DRUG BANK

DB01053

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

PRIMARY

MERCK INDEX

m8473

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

PRIMARY

Merck Index

INN

58

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

PRIMARY

CHEBI

18208

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

PRIMARY

EPA CompTox

DTXSID5046934

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

PRIMARY

CHEBI

51354

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

PRIMARY

LACTMED

Penicillin G

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

PRIMARY

PUBCHEM

5904

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

PRIMARY

HSDB

3166

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

PRIMARY

RXCUI

7980

Created by admin on Fri Dec 15 14:58:04 UTC 2023 , Edited by admin on Fri Dec 15 14:58:04 UTC 2023

PRIMARY

RxNorm

Related Record Type Details


					ZWJ2Y6JZWY

OAT-3

TRANSPORTER -> INHIBITOR


					17R794ESYN

PENICILLIN G PROCAINE

SALT/SOLVATE -> PARENT


					AF5F3C86Z1

DIBENZYLAMINE PENICILLIN G

SALT/SOLVATE -> PARENT

Amount:


					5UL276H6TF

CLEMIZOLE PENICILLIN

SALT/SOLVATE -> PARENT

Amount:


					66DDF797LP

OATP-8

TRANSPORTER -> INHIBITOR


					AIN96D6SGL

OATP1B1

TRANSPORTER -> SUBSTRATE


					Q42T66VG0C

EXCRETED UNCHANGED

Qualification:

URINE

Amount:


					PUC887544V

PENICILLIN G 2-AMINO-4-METHOXY-6-METHYLPYRIMIDINE

SALT/SOLVATE -> PARENT


					Z1GL5S1Z1Z

PENICILLIN G CALCIUM

SALT/SOLVATE -> PARENT


					46917D13T1

PYRIMIDINE PENICILLIN G

SALT/SOLVATE -> PARENT


					WH3RD005B0

PENICILLIN G BENZHYDRYLAMINE

SALT/SOLVATE -> PARENT


					RIT82F58GK

PENICILLIN G BENZATHINE

SALT/SOLVATE -> PARENT


					C3VTF4URW3

PENICILLIN G 2-AMINO-4-METHYLPYRIMIDINE

SALT/SOLVATE -> PARENT


					O3S7RWT8R5

BENETHAMINE PENICILLIN

SALT/SOLVATE -> PARENT

Amount:


					667Y1107D3

PENICILLIN G HYDRABAMINE

SALT/SOLVATE -> PARENT


					YS5LY7JF4N

PENICILLIN G SODIUM

SALT/SOLVATE -> PARENT

Amount:


					SSZ1S4I0US

PENICILLIN G BENZATHINE ANHYDROUS

SALT/SOLVATE -> PARENT


					VL775ZTH4C

PENICILLIN G POTASSIUM

SALT/SOLVATE -> PARENT


					M7PHE4F8HL

Penicillin G quinine

SALT/SOLVATE -> PARENT

Amount:


					6KXP5JH4YJ

2-AMINO-4-METHOXYPYRIMIDINE PENICILLIN G

SALT/SOLVATE -> PARENT

Related Record Type Details


					Z61I075U2W

PARENT -> IMPURITY

Interaction Type:

CHROMATOGRAPHIC PURITY (HPLC/UV)

Qualification:

EP

Amount:


					146T0TU1JB

PENICILLIN V POTASSIUM

PARENT -> IMPURITY

Interaction Type:

CHROMATOGRAPHIC PURITY (HPLC/UV)

Qualification:

EP

Amount:


					44MHH77OIC

PENICILLIN V BENZATHINE TETRAHYDRATE

PARENT -> IMPURITY

Amount:

Related Record Type Details


					Q42T66VG0C

ACTIVE MOIETY

Name	Property Type	Amount	Referenced Substance	Defining	Parameters	References
Cmax	PHARMACOKINETIC				ROUTE OF ADMINSTRATION PHARMACOKINETIC DOSE PHARMACOKINETIC Tmax PHARMACOKINETIC