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Compound Detail

CHEMBL261772

MECLOCYCLINE SULFOSALICYLATE
💊 Approved Drug
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💊 Approved Drug
C=C1c2c(Cl)ccc(O)c2C(=O)C2=C(O)[C@]3(O)C(=O)C(C(N)=O)=C(O)[C@@H](N(C)C)[C@@H]3[C@@H](O)[C@H]12.O=C(O)c1cc(S(=O)(=O)O)ccc1O

Basic Information

ChEMBL ID CHEMBL261772
Name MECLOCYCLINE SULFOSALICYLATE
Phase Approved
Structure Type MOL
InChI Key FYSVKUUNXYGFLA-CCHMMTNSSA-N
Therapeutic ✓ Yes

Known Names

Meclan Meclocil Meclocycline 5-sulfosalicylate Meclocycline sulfosalicylate Meclocyline sulfosalicylate Mecloderm Meclosorb NSC-757831 Quoderm SNX-1012 Traumatociclina
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
5
Publications
11
Known Names
2
Indications
1
Mechanisms

Molecular Properties

695.1
MW (Da)

Drug Information

Molecule Type Small molecule
First Approval 1982
Availability Discontinued
Chirality Single Enantiomer

Routes of Administration

Topical
USAN Stem -cycline; -fos-; -sal-
USAN Year 1980

Extended Properties

Molecular Formula C29H27ClN2O14S
MW 695.06

Mechanism of Action

Mechanism Action Type Target Direct Efficacy
Bacterial 70S ribosome inhibitor INHIBITOR Bacterial 70S ribosome

Indications

Stomatitis Stomatitis

Activity Summary

IC50 1 meas. best 6.6

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 6.6 6.6 250.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 250.0 nM 6.6 Inhibition of synthetic amyloid beta-42 oligomerization by ELISA 17284452

Literature References

PubMed DOI Target Context # Activities
17284452 10.1074/jbc.m608207200 Unchecked 4
19640715 10.1016/j.bmcl.2009.07.082 Unchecked 2
23571415 10.1124/mol.112.084152 Solute carrier organic anion transporter family member 1B3 1
23571415 10.1124/mol.112.084152 Solute carrier organic anion transporter family member 1B1 1
- 10.1101/2020.04.21.054387 SARS-CoV-2 1

Data from ChEMBL 36 via Core Engine