LYMECYCLINE

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National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C29H38N4O10
Molecular Weight	602.6328
Optical Activity	UNSPECIFIED
Defined Stereocenters	6 / 6
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of LYMECYCLINE

Structure Search

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)NCNCCCC[C@H](N)C(O)=O)=C(O)[C@H]2N(C)C

InChI

InChIKey=AHEVKYYGXVEWNO-UEPZRUIBSA-N

InChI=1S/C29H38N4O10/c1-28(42)13-7-6-9-17(34)18(13)22(35)19-14(28)11-15-21(33(2)3)23(36)20(25(38)29(15,43)24(19)37)26(39)32-12-31-10-5-4-8-16(30)27(40)41/h6-7,9,14-16,21,31,34,36-37,42-43H,4-5,8,10-12,30H2,1-3H3,(H,32,39)(H,40,41)/t14-,15-,16-,21-,28+,29-/m0/s1

HIDE SMILES / InChI

Molecular Formula	C29H38N4O10
Molecular Weight	602.6328
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	6 / 6
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

Substance Class	Chemical Created by `admin` on `Fri Dec 15 15:46:37 UTC 2023` Edited by `admin` on `Fri Dec 15 15:46:37 UTC 2023`
Record UNII	7D6EM3S13P
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

LYMECYCLINE

Official Name

English

CICLOLYSINE

Common Name

English

LYMECYCLINE [MI]

Common Name

English

TETRACYCLINE-L-METHYLENELYSINE

Common Name

English

(+)-N-(5-AMINO-5-CARBOXYPENTYLAMINOMETHYL)-4-DIMETHYLAMINO-1,4,4A,5,5A,6,11,12A-OCTAHYDRO-3,6,10,12,12A-PENTAHYDROXY-6-METHYL-1,11-DIOXONAPHTHACENE-2-CARBOXAMIDE

Common Name

English

CICLOLYSAL

Common Name

English

LYMECYCLINE [EP MONOGRAPH]

Common Name

English

LYMECYCLINE [MART.]

Common Name

English

Lymecycline [WHO-DD]

Common Name

English

TETRALYSAL

Brand Name

English

TETRACYCLINEMETHYLENELYSINE

Common Name

English

lymecycline [INN]

Common Name

English

MUCOMYCIN

Brand Name

English

Classification Tree Code System Code

NCI_THESAURUS

C1595

Created by admin on Fri Dec 15 15:46:37 UTC 2023 , Edited by admin on Fri Dec 15 15:46:37 UTC 2023

WHO-ATC

J01AA04

Created by admin on Fri Dec 15 15:46:37 UTC 2023 , Edited by admin on Fri Dec 15 15:46:37 UTC 2023

WHO-VATC

QJ01AA04

Created by admin on Fri Dec 15 15:46:37 UTC 2023 , Edited by admin on Fri Dec 15 15:46:37 UTC 2023

Code System Code Type Description

MESH

D008194

Created by admin on Fri Dec 15 15:46:37 UTC 2023 , Edited by admin on Fri Dec 15 15:46:37 UTC 2023

PRIMARY

ChEMBL

CHEMBL2103929

Created by admin on Fri Dec 15 15:46:37 UTC 2023 , Edited by admin on Fri Dec 15 15:46:37 UTC 2023

PRIMARY

DRUG CENTRAL

1619

Created by admin on Fri Dec 15 15:46:37 UTC 2023 , Edited by admin on Fri Dec 15 15:46:37 UTC 2023

PRIMARY

FDA UNII

7D6EM3S13P

Created by admin on Fri Dec 15 15:46:37 UTC 2023 , Edited by admin on Fri Dec 15 15:46:37 UTC 2023

PRIMARY

NCI_THESAURUS

C76991

Created by admin on Fri Dec 15 15:46:37 UTC 2023 , Edited by admin on Fri Dec 15 15:46:37 UTC 2023

PRIMARY

CAS

992-21-2

Created by admin on Fri Dec 15 15:46:37 UTC 2023 , Edited by admin on Fri Dec 15 15:46:37 UTC 2023

PRIMARY

EPA CompTox

DTXSID9045344

Created by admin on Fri Dec 15 15:46:37 UTC 2023 , Edited by admin on Fri Dec 15 15:46:37 UTC 2023

PRIMARY

DRUG BANK

DB00256

Created by admin on Fri Dec 15 15:46:37 UTC 2023 , Edited by admin on Fri Dec 15 15:46:37 UTC 2023

PRIMARY

CHEBI

59040

Created by admin on Fri Dec 15 15:46:37 UTC 2023 , Edited by admin on Fri Dec 15 15:46:37 UTC 2023

PRIMARY

INN

1679

Created by admin on Fri Dec 15 15:46:37 UTC 2023 , Edited by admin on Fri Dec 15 15:46:37 UTC 2023

PRIMARY

SMS_ID

100000081734

Created by admin on Fri Dec 15 15:46:37 UTC 2023 , Edited by admin on Fri Dec 15 15:46:37 UTC 2023

PRIMARY

ECHA (EC/EINECS)

213-592-2

Created by admin on Fri Dec 15 15:46:37 UTC 2023 , Edited by admin on Fri Dec 15 15:46:37 UTC 2023

PRIMARY

EVMPD

SUB08625MIG

Created by admin on Fri Dec 15 15:46:37 UTC 2023 , Edited by admin on Fri Dec 15 15:46:37 UTC 2023

PRIMARY

WIKIPEDIA

LYMECYCLINE

Created by admin on Fri Dec 15 15:46:37 UTC 2023 , Edited by admin on Fri Dec 15 15:46:37 UTC 2023

PRIMARY

MERCK INDEX

m6959

Created by admin on Fri Dec 15 15:46:37 UTC 2023 , Edited by admin on Fri Dec 15 15:46:37 UTC 2023

PRIMARY

Merck Index

RXCUI

6513

Created by admin on Fri Dec 15 15:46:37 UTC 2023 , Edited by admin on Fri Dec 15 15:46:37 UTC 2023

PRIMARY

RxNorm

Related Record Type Details


					7284RM98Q5

ANHYDROTETRACYCLINE

IMPURITY -> PARENT

Interaction Type:

CHROMATOGRAPHIC PURITY (HPLC/UV)

Qualification:

EP

Amount:


					WCK1KIQ23Q

CHLORTETRACYCLINE

IMPURITY -> PARENT

Comments:

sum of impurities D and G: not more than the area of the corresponding peak in the chromatogram obtained with reference solution (f) (0.5 per cent)

Interaction Type:

CHROMATOGRAPHIC PURITY (HPLC/UV)

Qualification:

EP


					KF6I0R5HOO

(4S,4AS,5AS,6S,12AS)-2-ACETYL-4-(DIMETHYLAMINO)-4A,5A,6,12A-TETRAHYDRO-3,6,10,12,12A-PENTAHYDROXY-6-METHYL-1,11(4H,5H)-NAPHTHACENEDIONE

IMPURITY -> PARENT

Interaction Type:

CHROMATOGRAPHIC PURITY (HPLC/UV)

Qualification:

EP

Amount:


					D12GU0X3KA

EPITETRACYCLINE

IMPURITY -> PARENT

Interaction Type:

CHROMATOGRAPHIC PURITY (HPLC/UV)

Qualification:

EP

Amount:


					F8VB5M810T

IMPURITY -> PARENT

Interaction Type:

CHROMATOGRAPHIC PURITY (HPLC/UV)

Qualification:

EP

Amount:


					680VDL31MX

4-EPIANHYDROTETRACYCLINE

IMPURITY -> PARENT

Comments:

sum of impurities D and G: not more than the area of the corresponding peak in the chromatogram obtained with reference solution (f) (0.5 per cent)

Interaction Type:

CHROMATOGRAPHIC PURITY (HPLC/UV)

Qualification:

EP

Related Record Type Details


					7D6EM3S13P

ACTIVE MOIETY