General
Preferred name
OXYTETRACYCLINE
Synonyms
Terramycin ()
OXYTETRACYCLINE HYDROCHLORIDE ()
Oxytetracycline Dihydrate ()
OXYTETRACYCLINE ANHYDROUS ()
Oxytetracycline (hydrochloride) ()
OXYTETRACYCLINE CALCIUM ()
Tetraplex ()
Oxytetracycline (anhydrous) ()
NSC-757262 ()
Hi-Tet ()
Oxytetracycline dihydrate ()
Unimycin ()
5-hydroxytetracycline dihydrate ()
Oxytetramix-250 ()
Terrafungine ()
Microtet ()
OXTC ()
Oxytetracyclinum dihydras ()
Berkmycen ()
Oxitetracycline ()
Terramycine ()
Chemocycline ()
Imperacin ()
Oxytetracycline dehydrate ()
Galenomycin ()
Nitox ()
Oxymycin ()
NSC-9169 ()
E703 ()
Oxytetracyclini hydrochloridum ()
Oxy-Kesso-Tetra ()
Oxytetracycline hcl ()
Calcium dioxytetracycline ()
Oxytetracycline hemicalcium ()
P&D ID
PD009901
CAS
6153-64-6
79-57-2
15251-48-6
7179-50-2
2058-46-0
Tags
natural product
drug
available
Approved by
FDA
First approval
1982
1964
Drug Status
investigational
approved
vet_approved
Max Phase
Phase 4
Drug indication
Antirickettsial
Antibacterial
Antibacterial,Antirickettsial
Structure
Probe scores
P&D probe-likeness score
[[ v.score ]]%
Structure formats
[[ format ]]
[[ compound[format === 'MOL' ? 'molblock' : format.toLowerCase()] ]]
Cell lines
1
Organisms
1
Compound Sets
18
Cayman Chemical Bioactives
18076
ChEMBL Approved Drugs
CHEMBL1607480
CHEMBL1517
CHEMBL3989568
ChEMBL Drugs
CHEMBL1607480
CHEMBL1517
CHEMBL3989568
DrugBank
DB00595
DrugBank Approved Drugs
DB00595
DrugCentral
2041
DrugCentral Approved Drugs
2041
Enamine BioReference Compounds
LSP-MoA library (Laboratory of Systems Pharmacology)
CHEMBL1607480
CHEMBL1517
MedChem Express Bioactive Compound Library
HY-B0275A
HY-B0275
NCATS Inxight Approved Drugs
SLF0D9077S
NPC Screening Collection
Other bioactive compounds
Prestwick Chemical Library
ReFrame library
Selleckchem Bioactive Compound Library
oxytetracycline-dihydrate
TargetMol Bioactive Compound Library
T0895
The Spectrum Collection
External IDs
83
Properties
(calculated by RDKit )
Molecular Weight
460.15
Hydrogen Bond Acceptors
10
Hydrogen Bond Donors
7
Rotatable Bonds
2
Ring Count
4
Aromatic Ring Count
1
cLogP
-1.24
TPSA
201.85
Fraction CSP3
0.41
Chiral centers
6.0
Largest ring
6.0
QED
0.26
Structural alerts
0
No structural alerts detected
Related compounds
Custom attributes
(extracted from source data)
Pathway
Microbiology&virology
Anti-infection
Metabolic Enzyme/Protease
Target
16S ribosome
30S ribosome
antibiotic
Bacterial
Endogenous Metabolite
HSV
Antibiotics,Bacterial
Source data