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Details

Stereochemistry ABSOLUTE
Molecular Formula C22H21ClN2O8.C7H6O6S
Molecular Weight 695.048
Optical Activity UNSPECIFIED
Defined Stereocenters 5 / 5
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MECLOCYCLINE SULFOSALICYLATE

SMILES

OC(=O)C1=C(O)C=CC(=C1)S(O)(=O)=O.CN(C)[C@H]2[C@@H]3[C@@H](O)[C@@H]4C(=C)C5=C(Cl)C=CC(O)=C5C(=O)C4=C(O)[C@]3(O)C(=O)C(C(N)=O)=C2O

InChI

InChIKey=FYSVKUUNXYGFLA-CCHMMTNSSA-N
InChI=1S/C22H21ClN2O8.C7H6O6S/c1-6-9-7(23)4-5-8(26)11(9)16(27)12-10(6)17(28)14-15(25(2)3)18(29)13(21(24)32)20(31)22(14,33)19(12)30;8-6-2-1-4(14(11,12)13)3-5(6)7(9)10/h4-5,10,14-15,17,26,28-30,33H,1H2,2-3H3,(H2,24,32);1-3,8H,(H,9,10)(H,11,12,13)/t10-,14-,15+,17+,22+;/m1./s1

HIDE SMILES / InChI
Molecular Formula C22H21ClN2O8
Molecular Weight 476.864
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 5 / 5
E/Z Centers 0
Optical Activity UNSPECIFIED
Molecular Formula C7H6O6S
Molecular Weight 218.184
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description

Meclocycline is a tetracycline antibiotic. It is used topically for skin infections treatment. Tetracyclines are broad-spectrum bacteriostatic agents and act by inhibiting protein synthesis by blocking the binding of aminoacyl tRNA (transfer RNA) to the mRNA (messenger RNA) ribosome complex. Meclocycline might increase sensitivity to light when it is used with Aminolevulinic acid.

Originator

Blackwood, R.K.
2
Sources: DOI: 10.1021/ja00907a010
Curator's Comment: https://books.google.ru/books?id=0vXTBwAAQBAJ&pg=PA757&lpg=PA757&dq=Meclocycline+1982&source=bl&ots=6IUep2UBpy&sig=cQZ9OF2ixsk8j9wP_oZtJS_iLt0&hl=ru&sa=X&ved=0ahUKEwie2ZidkILMAhXC2CwKHTAtDlkQ6AEIHjAA#v=onepage&q=Meclocycline%201982&f=false

Approval Year

1980
62
Targets

Targets

Primary TargetPharmacologyConditionPotency
Binding Agent
1076
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
Approved
8583
MECLAN

Approved Use

Topical treatment of inflammatory acne vulgaris

Launch Date

1981
Doses

Doses

DosePopulationAdverse events​
1 % 2 times / day multiple, topical
Recommended
Dose: 1 %, 2 times / day
Route: topical
Route: multiple
Dose: 1 %, 2 times / day
Sources:
https://pubmed.ncbi.nlm.nih.gov/1675534
unhealthy, 12-37
Health Status: unhealthy
Age Group: 12-37
Sex: M+F
Sources:
https://pubmed.ncbi.nlm.nih.gov/1675534
Other AEs: Yellow skin...
Other AEs:
Yellow skin (6%)
Sources:
https://pubmed.ncbi.nlm.nih.gov/1675534
1 % 2 times / day multiple, topical
Recommended
Dose: 1 %, 2 times / day
Route: topical
Route: multiple
Dose: 1 %, 2 times / day
Sources:
https://pubmed.ncbi.nlm.nih.gov/6452987
unhealthy
Health Status: unhealthy
Sources:
https://pubmed.ncbi.nlm.nih.gov/6452987
Other AEs: Contact dermatitis...
Other AEs:
Contact dermatitis
Sources:
https://pubmed.ncbi.nlm.nih.gov/6452987
AEs

AEs

AESignificanceDosePopulation
Yellow skin 6%
1 % 2 times / day multiple, topical
Recommended
Dose: 1 %, 2 times / day
Route: topical
Route: multiple
Dose: 1 %, 2 times / day
Sources:
https://pubmed.ncbi.nlm.nih.gov/1675534
unhealthy, 12-37
Health Status: unhealthy
Age Group: 12-37
Sex: M+F
Sources:
https://pubmed.ncbi.nlm.nih.gov/1675534
Contact dermatitis
1 % 2 times / day multiple, topical
Recommended
Dose: 1 %, 2 times / day
Route: topical
Route: multiple
Dose: 1 %, 2 times / day
Sources:
https://pubmed.ncbi.nlm.nih.gov/6452987
unhealthy
Health Status: unhealthy
Sources:
https://pubmed.ncbi.nlm.nih.gov/6452987
Sourcing

Sourcing

Vendor/AggregatorIDURL
ABI Chem
AC1L27GB
ABI Chem
AC1NR077
ABI Chem
AC1NSE5G
Alfa Chemistry
2013-58-3
https://www.alfa-chemistry.com/cas_2013-58-3.htm
AmicBase - Antimicrobial Activities
4057
BioSynth
J-013043
https://www.biosynth.com/en/products/all-products/products/J-013043.html
Chemieliva Pharmaceutical Co., Ltd
PBCM1229533
ChemMol
44014818
http://www.chemmol.com/chemmol/44014818.html
ChemMol
99047357
http://www.chemmol.com/chemmol/99047357.html
Compound Cloud
54676538
Compound Cloud
54676539
DC Chemicals
DC36400
http://www.dcchemicals.com//product_show-GS-2989.html
eMolecules
295160563
Molnova
M15822
MuseChem
R074533
https://www.musechem.com/product/R074533.html
NovoSeek
5282519
NovoSeek
5359674
Smolecule
S534870
http://www.smolecule.com/products/s534870
TargetMol
T0281
THE BioTek
bt-274529
https://www.thebiotek.com/product/inhibitors/bt-274529
Yick-Vic Chemicals & Pharmaceuticals (HK) Ltd.
PH-0154A
ZINC
ZINC000004149268
http://zinc15.docking.org/substances/ZINC000004149268
PubMed

PubMed

TitleDatePubMed
Cell-based and cytokine-directed chemical screen to identify potential anti-multiple myeloma agents.
2010-07
Patents

Patents

06683067
2
06893665
2
06946118
2
JP2002511777A
420
JP2003515526A
470
JP2009526755A
475
JP2012500274A
13

Sample Use Guides

In Vivo Use Guide
Curator's Comment: Noticeable improvement may be seen in 4 to 6 weeks. In some patients it may require up to 6 to 8 weeks of treatment before noticeable improvement is seen and up to 8 to 12 weeks before maximum benefit is seen.
Two times a day, morning and evening.
Route of Administration: Topical
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:51:51 GMT 2025
Edited
by admin
on Mon Mar 31 17:51:51 GMT 2025
Record UNII
46VZA7RX2B
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MECLOCYCLINE 5-SULFOSALICYLATE
MI  
Preferred Name English
MECLOCYCLINE SULFOSALICYLATE
MART.   ORANGE BOOK   USAN   USP   USP-RS   WHO-DD  
USAN  
Official Name English
MECLOCYCLINE SULFOSALICYLATE [MART.]
Common Name English
MECLOCYCLINE SULFOSALICYLATE [ORANGE BOOK]
Common Name English
MECLOCYCLINE SULFOSALICYLATE [USP-RS]
Common Name English
NSC-757831
Code English
MECLOCYCLINE SULFOSALICYLATE [USP IMPURITY]
Common Name English
MECLAN
Brand Name English
SNX-1012
Code English
MECLOCYCLINE SULFOSALICYLATE [USAN]
Common Name English
Meclocycline sulfosalicylate [WHO-DD]
Common Name English
MECLOCYCLINE 5-SULFOSALICYLATE [MI]
Common Name English
(4S,4aR,5S,5aR,12aS)-7-Chloro-4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,10,12,12a-pentahydroxy-6-methylene-1,11-dioxo-2-naphthacenecarboxamide mono(5-sulfosalicylate) (salt)
Common Name English
2-NAPHTHACENECARBOXAMIDE, 7-CHLORO-4-(DIMETHYLAMINO)-1,4,4A,5,5A,6,11,12A-OCTAHYDRO-3,5,10,12,12A-PENTAHYDROXY-6-METHYLENE-1,11-DIOXO-, (4S-(4.ALPHA.,4A.ALPHA.,5.ALPHA.,5A.ALPHA.,12A.ALPHA.))-, MONO(2-HYDROXY-5-SULFOBENZOATE) (SALT)
Common Name English
MECLOCYLINE SULFOSALICYLATE [VANDF]
Common Name English
MECLOCYLINE SULFOSALICYLATE
VANDF  
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C1595
Created by admin on Mon Mar 31 17:51:51 GMT 2025 , Edited by admin on Mon Mar 31 17:51:51 GMT 2025
Code System Code Type Description
RS_ITEM_NUM
1377508
Created by admin on Mon Mar 31 17:51:51 GMT 2025 , Edited by admin on Mon Mar 31 17:51:51 GMT 2025
PRIMARY
DRUG BANK
DBSALT002414
Created by admin on Mon Mar 31 17:51:51 GMT 2025 , Edited by admin on Mon Mar 31 17:51:51 GMT 2025
PRIMARY
FDA UNII
46VZA7RX2B
Created by admin on Mon Mar 31 17:51:51 GMT 2025 , Edited by admin on Mon Mar 31 17:51:51 GMT 2025
PRIMARY
CAS
73816-42-9
Created by admin on Mon Mar 31 17:51:51 GMT 2025 , Edited by admin on Mon Mar 31 17:51:51 GMT 2025
PRIMARY
ChEMBL
CHEMBL261772
Created by admin on Mon Mar 31 17:51:51 GMT 2025 , Edited by admin on Mon Mar 31 17:51:51 GMT 2025
PRIMARY
NCI_THESAURUS
C47596
Created by admin on Mon Mar 31 17:51:51 GMT 2025 , Edited by admin on Mon Mar 31 17:51:51 GMT 2025
PRIMARY
EVMPD
SUB03105MIG
Created by admin on Mon Mar 31 17:51:51 GMT 2025 , Edited by admin on Mon Mar 31 17:51:51 GMT 2025
PRIMARY
EPA CompTox
DTXSID5045596
Created by admin on Mon Mar 31 17:51:51 GMT 2025 , Edited by admin on Mon Mar 31 17:51:51 GMT 2025
PRIMARY
ECHA (EC/EINECS)
277-614-2
Created by admin on Mon Mar 31 17:51:51 GMT 2025 , Edited by admin on Mon Mar 31 17:51:51 GMT 2025
PRIMARY
SMS_ID
100000086163
Created by admin on Mon Mar 31 17:51:51 GMT 2025 , Edited by admin on Mon Mar 31 17:51:51 GMT 2025
PRIMARY
NSC
757831
Created by admin on Mon Mar 31 17:51:51 GMT 2025 , Edited by admin on Mon Mar 31 17:51:51 GMT 2025
PRIMARY
RXCUI
203162
Created by admin on Mon Mar 31 17:51:51 GMT 2025 , Edited by admin on Mon Mar 31 17:51:51 GMT 2025
PRIMARY RxNorm
MERCK INDEX
m7119
Created by admin on Mon Mar 31 17:51:51 GMT 2025 , Edited by admin on Mon Mar 31 17:51:51 GMT 2025
PRIMARY Merck Index
Related Record Type Details
Structure of SULFOSALICYLIC ACID
PARENT -> SALT/SOLVATE
Structure of MECLOCYCLINE
PARENT -> SALT/SOLVATE
Related Record Type Details
Structure of MECLOCYCLINE
ACTIVE MOIETY
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NCATS
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