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Details

Stereochemistry ABSOLUTE
Molecular Formula C16H18N2O4S.C13H20N2O2.H2O
Molecular Weight 588.716
Optical Activity UNSPECIFIED
Defined Stereocenters 3 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PENICILLIN G PROCAINE

SMILES

O.CCN(CC)CCOC(=O)C1=CC=C(N)C=C1.[H][C@]23SC(C)(C)[C@@H](N2C(=O)[C@H]3NC(=O)CC4=CC=CC=C4)C(O)=O

InChI

InChIKey=KZDCMKVLEYCGQX-UDPGNSCCSA-N
InChI=1S/C16H18N2O4S.C13H20N2O2.H2O/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;1-3-15(4-2)9-10-17-13(16)11-5-7-12(14)8-6-11;/h3-7,11-12,14H,8H2,1-2H3,(H,17,19)(H,21,22);5-8H,3-4,9-10,14H2,1-2H3;1H2/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
Molecular Formula C13H20N2O2
Molecular Weight 236.3101
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE
Molecular Formula H2O
Molecular Weight 18.0153
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
123738
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:16:27 UTC 2023
Edited
by admin
on Fri Dec 15 16:16:27 UTC 2023
Record UNII
17R794ESYN
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PENICILLIN G PROCAINE
GREEN BOOK   MI   ORANGE BOOK   USP   USP-RS   VANDF  
Common Name English
Procaine benzylpenicillin [WHO-DD]
Common Name English
BENZYLPENICILLIN PROCAINE
Common Name English
PENICILLIN G PROCAINE [VANDF]
Common Name English
4-THIA-1-AZABICYCLO(3.2.0)HEPTANE-2-CARBOXYLIC ACID, 3,3-DIMETHYL-7-OXO-6-((PHENYLACETYL)AMINO)- (2S,5R,6R)-, COMPD. WITH 2-(DIETHYLAMINO)ETHYL 4-AMINOBENZOATE, HYDRATE (1:1:1)
Common Name English
DURACILLIN A.S.
Brand Name English
BICILLIN C-R COMPONENT PENICILLIN G PROCAINE
Common Name English
PROCAINE BENZYLPENICILLIN
MART.   WHO-DD   WHO-IP  
Common Name English
PROCAINI BENZYLPENICILLINUM [WHO-IP LATIN]
Common Name English
PROCAINE PENICILLIN G MONOHYDRATE
Common Name English
PENICILLIN G PROCAINE [USP MONOGRAPH]
Common Name English
PENICILLIN G PROCAINE COMPONENT OF BICILLIN C-R
Common Name English
4-THIA-1-AZABICYCLO(3.2.0)HEPTANE-2-CARBOXYLIC ACID, 3,3-DIMETHYL-7-OXO-6-((PHENYLACETYL)AMINO)-, (2S-(2.ALPHA.,5.ALPHA.,6.BETA.))-, COMPD. WITH 2-(DIETHYLAMINO)ETHYL 4-AMINOBENZOATE (1:1) MONOHYDRATE
Common Name English
PENICILLIN G PROCAINE [USP-RS]
Common Name English
PROCAINE PENICILLIN G
Common Name English
PROCAINE BENZYLPENICILLIN [WHO-IP]
Common Name English
CRYSTICILLIN A.S.
Brand Name English
PENICILLIN G PROCAINE [ORANGE BOOK]
Common Name English
PFIZERPEN-AS
Brand Name English
PENICILLIN G PROCAINE [MI]
Common Name English
PENICILLIN G PROCAINE [GREEN BOOK]
Common Name English
PROCAINE PENICILLIN
Common Name English
PROCAINE BENZYLPENICILLIN [MART.]
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 COMPOUND WITH 2-(DIETHYLAMINO)ETHYL P-AMINOBENZOATE (1:1) MONOHYDRATE
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C1500
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
CFR 21 CFR 526.1696B
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
WHO-VATC QG51AG01
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
CFR 21 CFR 526.1696C
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
WHO-ATC J01CE09
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
CFR 21 CFR 558.145
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
CFR 21 CFR 526.1696A
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
WHO-ESSENTIAL MEDICINES LIST 6.2.1
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
CFR 21 CFR 522.1696
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
WHO-VATC QJ51RC04
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
CFR 21 CFR 522.1696A
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
WHO-VATC QJ01CE09
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
CFR 21 CFR 522.1696C
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
CFR 21 CFR 526.1696D
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
CFR 21 CFR 558.145
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
WHO-VATC QJ51CE09
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
WHO-VATC QJ51CE59
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
CFR 21 CFR 522.1696B
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
WHO-VATC QJ51RC23
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
Code System Code Type Description
CAS
6130-64-9
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
PRIMARY
WIKIPEDIA
PROCAINE BENZYLPENICILLIN
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
PRIMARY
CHEBI
52154
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
PRIMARY
RS_ITEM_NUM
1502552
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
PRIMARY
DRUG BANK
DB09320
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
PRIMARY
LACTMED
Procaine Penicillin G
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
PRIMARY
RXCUI
7983
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
PRIMARY RxNorm
EPA CompTox
DTXSID40210207
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
PRIMARY
EVMPD
SUB22648
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
ALTERNATIVE
MESH
D010402
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
PRIMARY
MERCK INDEX
m8476
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
PRIMARY Merck Index
FDA UNII
17R794ESYN
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
PRIMARY
EVMPD
SUB00752MIG
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
PRIMARY
WHO INTERNATIONAL PHARMACOPEIA
PENICILLIN G PROCAINE
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
PRIMARY Description: A white or almost white, crystalline powder; odourless or almost odourless. Solubility: Slightly soluble in water; soluble in ethanol (~750 g/l) TS. Category: Antibacterial drug. Storage: Procaine benzylpenicillin should be kept in a tightly closed container and protected from light. Labelling: The designation sterile Procaine benzylpenicillin indicates that the substance complies with the additional requirementsfor sterile Procaine benzylpenicillin and may be used for parenteral administration or for other sterile applications. Additional information: Solutions of Procaine benzylpenicillin are dextrorotatory. It is readily decomposed by acids, alkalis, andoxidizing agents. Even in the absence of light, it is gradually degraded on exposure to a humid atmosphere, the decompositionbeing faster at higher temperatures.
ChEMBL
CHEMBL1628385
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
PRIMARY
DAILYMED
17R794ESYN
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
PRIMARY
SMS_ID
100000088581
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
PRIMARY
DRUG CENTRAL
4459
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
PRIMARY
NCI_THESAURUS
C87370
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
PRIMARY
PUBCHEM
22502
Created by admin on Fri Dec 15 16:16:27 UTC 2023 , Edited by admin on Fri Dec 15 16:16:27 UTC 2023
PRIMARY
Related Record Type Details
Structure of PROCAINE
PARENT -> SALT/SOLVATE
Structure of PENICILLIN G
PARENT -> SALT/SOLVATE
Structure of PENICILLIN G PROCAINE ANHYDROUS
ANHYDROUS->SOLVATE
Related Record Type Details
BENZYLPENICILLOIC ACID
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of AMINOBENZOIC ACID
IMPURITY -> PARENT
Structure of BENZYLPENILLIC ACID
IMPURITY -> PARENT
Related Record Type Details
Structure of PENICILLIN G
ACTIVE MOIETY
Structure of PROCAINE
ACTIVE MOIETY
NIH
NCATS
PRIVACY ACT
ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
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