U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C29H38N8O8
Molecular Weight 626.6608
Optical Activity UNSPECIFIED
Defined Stereocenters 5 / 5
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GUAMECYCLINE

SMILES

[H][C@@]12C[C@@]3([H])C(C(=O)C4=C(C=CC=C4O)[C@@]3(C)O)=C(O)[C@]1(O)C(=O)C(C(=O)NCN5CCN(CC5)C(=N)NC(N)=N)=C(O)[C@H]2N(C)C

InChI

InChIKey=DIRJDIBCAHCCFL-AQFAATAFSA-N
InChI=1S/C29H38N8O8/c1-28(44)13-5-4-6-16(38)17(13)21(39)18-14(28)11-15-20(35(2)3)22(40)19(24(42)29(15,45)23(18)41)25(43)33-12-36-7-9-37(10-8-36)27(32)34-26(30)31/h4-6,14-15,20,38,40-41,44-45H,7-12H2,1-3H3,(H,33,43)(H5,30,31,32,34)/t14-,15-,20-,28+,29-/m0/s1

HIDE SMILES / InChI

Molecular Formula C29H38N8O8
Molecular Weight 626.6608
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 5 / 5
E/Z Centers 0
Optical Activity UNSPECIFIED

Guamecycline, a tetracycline derivative was studied in patients with broncho-pulmonary diseases and for the treatment of acute pneumopathies. However, information about the current use of this compound is not available.

Approval Year

PubMed

PubMed

TitleDatePubMed
Guamecycline in bronchial infections due to Diplococcus pneumoniae.
1972 Jan-Feb
Patents

Sample Use Guides

Unknown
Route of Administration: Respiratory
Substance Class Chemical
Created
by admin
on Sat Dec 16 16:21:22 GMT 2023
Edited
by admin
on Sat Dec 16 16:21:22 GMT 2023
Record UNII
4NQR4R6G3S
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GUAMECYCLINE
INN   MI   WHO-DD  
INN  
Official Name English
Guamecycline [WHO-DD]
Common Name English
GUAMECYCLINE [MI]
Common Name English
guamecycline [INN]
Common Name English
N-((4-(AMIDINOAMIDINO)-1-PIPERAZINYL)METHYL)-4-(DIMETHYLAMINO)-1,4,4A,5,5A,6,11,12A-OCTAHYDRO-3,6,10,12,12A-PENTAHYDROXY-6-METHYL-1,11-DIOXO-2-NAPHTHACENECARBOXAMIDE
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C1595
Created by admin on Sat Dec 16 16:21:22 GMT 2023 , Edited by admin on Sat Dec 16 16:21:22 GMT 2023
Code System Code Type Description
FDA UNII
4NQR4R6G3S
Created by admin on Sat Dec 16 16:21:22 GMT 2023 , Edited by admin on Sat Dec 16 16:21:22 GMT 2023
PRIMARY
MESH
C001312
Created by admin on Sat Dec 16 16:21:22 GMT 2023 , Edited by admin on Sat Dec 16 16:21:22 GMT 2023
PRIMARY
EVMPD
SUB07977MIG
Created by admin on Sat Dec 16 16:21:22 GMT 2023 , Edited by admin on Sat Dec 16 16:21:22 GMT 2023
PRIMARY
NCI_THESAURUS
C90947
Created by admin on Sat Dec 16 16:21:22 GMT 2023 , Edited by admin on Sat Dec 16 16:21:22 GMT 2023
PRIMARY
ECHA (EC/EINECS)
240-611-1
Created by admin on Sat Dec 16 16:21:22 GMT 2023 , Edited by admin on Sat Dec 16 16:21:22 GMT 2023
PRIMARY
MERCK INDEX
m1182
Created by admin on Sat Dec 16 16:21:22 GMT 2023 , Edited by admin on Sat Dec 16 16:21:22 GMT 2023
PRIMARY Merck Index
CAS
16545-11-2
Created by admin on Sat Dec 16 16:21:22 GMT 2023 , Edited by admin on Sat Dec 16 16:21:22 GMT 2023
PRIMARY
WIKIPEDIA
Xanthomycin A
Created by admin on Sat Dec 16 16:21:22 GMT 2023 , Edited by admin on Sat Dec 16 16:21:22 GMT 2023
PRIMARY
SMS_ID
100000084450
Created by admin on Sat Dec 16 16:21:22 GMT 2023 , Edited by admin on Sat Dec 16 16:21:22 GMT 2023
PRIMARY
ChEMBL
CHEMBL2103960
Created by admin on Sat Dec 16 16:21:22 GMT 2023 , Edited by admin on Sat Dec 16 16:21:22 GMT 2023
PRIMARY
DRUG CENTRAL
3273
Created by admin on Sat Dec 16 16:21:22 GMT 2023 , Edited by admin on Sat Dec 16 16:21:22 GMT 2023
PRIMARY
EPA CompTox
DTXSID301043159
Created by admin on Sat Dec 16 16:21:22 GMT 2023 , Edited by admin on Sat Dec 16 16:21:22 GMT 2023
PRIMARY
INN
2705
Created by admin on Sat Dec 16 16:21:22 GMT 2023 , Edited by admin on Sat Dec 16 16:21:22 GMT 2023
PRIMARY
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