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Details

Stereochemistry ABSOLUTE
Molecular Formula C21H21ClN2O8.ClH
Molecular Weight 501.314
Optical Activity UNSPECIFIED
Defined Stereocenters 5 / 5
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DEMECLOCYCLINE HYDROCHLORIDE

SMILES

Cl.[H][C@]12C[C@@]3([H])[C@H](N(C)C)C(O)=C(C(N)=O)C(=O)[C@@]3(O)C(O)=C1C(=O)C4=C(O)C=CC(Cl)=C4[C@H]2O

InChI

InChIKey=GVSJQNRGSCOSNJ-KBHRXELFSA-N
InChI=1S/C21H21ClN2O8.ClH/c1-24(2)14-7-5-6-10(16(27)12-9(25)4-3-8(22)11(12)15(6)26)18(29)21(7,32)19(30)13(17(14)28)20(23)31;/h3-4,6-7,14-15,25-26,28-29,32H,5H2,1-2H3,(H2,23,31);1H/t6-,7-,14-,15-,21-;/m0./s1

HIDE SMILES / InChI
Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE
Molecular Formula C21H21ClN2O8
Molecular Weight 464.853
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 5 / 5
E/Z Centers 0
Optical Activity UNSPECIFIED

Description
Curator's Comment: Description was created based on several sources, including https://www.drugs.com/ppa/demeclocycline.html | https://www.ncbi.nlm.nih.gov/pubmed/24154696

Demeclocycline hydrochloride is an antibiotic isolated from a mutant strain of Streptomyces aureofaciens. It inhibits protein synthesis by binding with the 30S and possibly the 50S ribosomal subunit(s) of susceptible bacteria. Demeclocycline has antimicrobial activity against a wide range of gram-negative and gram-positive organisms. Demeclocycline is indicated in the treatment of infections caused by susceptible strains of the designated microorganisms. Demeclocycline is currently used to treat hyponatremia in patients with the syndrome of inappropriate antidiuretic hormone secretion (SIADH). Demeclocycline mainly attenuates hyponatremia in SIADH by reducing adenylate cyclase 5/6 expression and, consequently, cAMP generation, AQP2 gene transcription, and AQP2 abundance in the renal inner medulla, coinciding with a reduced vasopressin escape response in other collecting duct segments.

CNS Activity

CNS Active
3913
Curator's Comment: Demeclocycline is CNS active in rodents. No human data available.

Originator

American Cyanamid
37
Curator's Comment: reference retrieved from http://www.drugfuture.com/chemdata/demeclocycline.html

Approval Year

1959
138
Targets

Targets

Primary TargetPharmacologyConditionPotency
Inhibitor
8297
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
Approved
8429
DEMECLOCYCLINE HYDROCHLORIDE

Approved Use

Demeclocycline HCl tablets, USP are indicated in the treatment of infections caused by susceptible strains of the designated microorganisms in the conditions below: Rocky Mountain spotted fever, typhus fever and the typhus group, Q fever, rickettsialpox and tick fevers caused by rickettsiae; Respiratory tract infections caused by Mycoplasma pneumoniae Lymphogranuloma venereum due to Chlamydia trachomatis Psittacosis (Ornithosis) due to Chlamydia psittaci Trachoma due to Chlamydia trachomatis, although the infectious agent is not always eliminated as judged by immunofluorescence Inclusion conjunctivitis caused by Chlamydia trachomatis Nongonococcal urethritis in adults caused by Ureaplasma urealyticum or Chlamydia trachomatis Relapsing fever due to Borrelia recurrentis Chancroid caused by Haemophilus ducreyi Plague due to Yersinia pestis Tularemia due to Francisella tularensis Cholera caused by Vibrio cholerae Campylobacter fetus infections cause by Campylobacter fetus Brucellosis due to Brucella species (in conjunction with streptomycin); Bartonellosis due to Bartonella bacilliformis Granuloma inguinale caused by Calymmatobacterium granulomatis Demeclocycline HCl tablets, USP are indicated for treatment of infections by the following gram-negative microorganisms, when bacteriologic testing indicates appropriate susceptibility to the drug: Escherichia coli Enterobacter aerogenes Shigella species Acinetobacter species Respiratory tract infections caused by Haemophilus influenzae Respiratory tract and urinary tract infections caused by Klebsiella species Demeclocycline HCl tablets, USP are indicated for treatment of infections caused by the following gram-positive microorganisms, when bacteriologic testing indicates appropriate susceptibility to the drug: Upper respiratory infections caused by Streptococcus pneumoniae Skin and skin structure infections caused by Staphylococcus aureus. (Note: Tetracyclines, including Demeclocycline, are not the drugs of choice in the treatment of any type of staphylococcal infection). When penicillin is contraindicated, tetracyclines, including Demeclocycline HCl, USP, are alternative drugs in the treatment of the following infections: Uncomplicated urethritis in men due to Neisseria gonorrhoeae, and for the treatment of other uncomplicated gonococcal infections Infections in women caused by Neisseria gonorrhoeae Syphilis caused by Treponema pallidum subspecies pallidum Yaws caused by Treponema pallidum subspecies pertenue Listeriosis due to Listeria monocytogenes Anthrax due to Bacillus anthracis Vincent’s infection caused by Fusobacterium fusiforme Actinomycosis caused by Actinomyces israelii Clostridial diseases caused by Clostridium species In acute intestinal amebiasis, Demeclocycline HCl, USP may be a useful adjunct to amebicides. In severe acne, Demeclocycline HCl, USP may be a useful adjunctive therapy. To reduce the development of drug-resistant bacteria and maintain the effectiveness of Demeclocycline HCl tablets, USP and other antibacterial drugs, Demeclocycline HCl tablets, USP should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. When culture and susceptibility information are available they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy.
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
2.4 mg/L
OTHER
https://www.medicines.org.uk/emc/product/499/smpc#PHARMACOKINETIC_PROPS
300 mg single, oral
dose: 300 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
DEMECLOCYCLINE plasma
Homo sapiens
population: UNKNOWN
age: UNKNOWN
sex: UNKNOWN
food status: UNKNOWN
1.2 mg/L
REVIEW
https://academic.oup.com/jac/article/58/2/256/718565
150 mg single, oral
dose: 150 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
DEMECLOCYCLINE serum
Homo sapiens
population: UNKNOWN
age: UNKNOWN
sex: UNKNOWN
food status: UNKNOWN
1.7 mg/L
REVIEW
https://academic.oup.com/jac/article/58/2/256/718565
300 mg single, oral
dose: 300 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
DEMECLOCYCLINE serum
Homo sapiens
population: UNKNOWN
age: UNKNOWN
sex: UNKNOWN
food status: UNKNOWN
2.5 mg/L
REVIEW
https://academic.oup.com/jac/article/58/2/256/718565
500 mg single, oral
dose: 500 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
DEMECLOCYCLINE serum
Homo sapiens
population: UNKNOWN
age: UNKNOWN
sex: UNKNOWN
food status: UNKNOWN
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
13 h
DRUG LABEL
https://www.accessdata.fda.gov/drugsatfda_docs/label/2012/050261s101lbl.pdf
150 mg single, oral
dose: 150 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
DEMECLOCYCLINE plasma
Homo sapiens
population: UNKNOWN
age: UNKNOWN
sex: UNKNOWN
food status: UNKNOWN
13.5 h
REVIEW
https://academic.oup.com/jac/article/58/2/256/718565
300 mg single, oral
dose: 300 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
DEMECLOCYCLINE serum
Homo sapiens
population: UNKNOWN
age: UNKNOWN
sex: UNKNOWN
food status: UNKNOWN
13 h
REVIEW
https://academic.oup.com/jac/article/58/2/256/718565
500 mg single, oral
dose: 500 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
DEMECLOCYCLINE serum
Homo sapiens
population: UNKNOWN
age: UNKNOWN
sex: UNKNOWN
food status: UNKNOWN
Funbound

Funbound

ValueDoseCo-administeredAnalytePopulation
60%
DRUG LABEL
https://www.accessdata.fda.gov/drugsatfda_docs/label/2012/050261s101lbl.pdf
150 mg single, oral
dose: 150 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
DEMECLOCYCLINE plasma
Homo sapiens
population: UNKNOWN
age: UNKNOWN
sex: UNKNOWN
food status: UNKNOWN
17%
REVIEW
https://academic.oup.com/jac/article/58/2/256/718565
150 mg single, oral
dose: 150 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
DEMECLOCYCLINE serum
Homo sapiens
population: UNKNOWN
age: UNKNOWN
sex: UNKNOWN
food status: UNKNOWN
10%
DRUG LABEL
https://www.accessdata.fda.gov/drugsatfda_docs/label/2012/050261s101lbl.pdf
DEMECLOCYCLINE plasma
Homo sapiens
Doses

Doses

DosePopulationAdverse events​
600 mg 4 times / day multiple, oral
Highest studied dose
Dose: 600 mg, 4 times / day
Route: oral
Route: multiple
Dose: 600 mg, 4 times / day
Sources:
https://pubmed.ncbi.nlm.nih.gov/103083/
unhealthy, 64 years
n = 1
Health Status: unhealthy
Condition: meningitis
Age Group: 64 years
Sex: M
Population Size: 1
Sources:
https://pubmed.ncbi.nlm.nih.gov/103083/
Disc. AE: Nephrotoxicity...
AEs leading to
discontinuation/dose reduction:
Nephrotoxicity
Sources:
https://pubmed.ncbi.nlm.nih.gov/103083/
150 mg 4 times / day multiple, oral
Dose: 150 mg, 4 times / day
Route: oral
Route: multiple
Dose: 150 mg, 4 times / day
Sources:
https://www.accessdata.fda.gov/drugsatfda_docs/label/2012/050261s101lbl.pdf
pregnant
Health Status: pregnant
Sex: F
Sources:
https://www.accessdata.fda.gov/drugsatfda_docs/label/2012/050261s101lbl.pdf
Disc. AE: Fetal damage...
AEs leading to
discontinuation/dose reduction:
Fetal damage (grade 5)
Sources:
https://www.accessdata.fda.gov/drugsatfda_docs/label/2012/050261s101lbl.pdf
150 mg 4 times / day multiple, oral
Dose: 150 mg, 4 times / day
Route: oral
Route: multiple
Dose: 150 mg, 4 times / day
Sources:
https://www.accessdata.fda.gov/drugsatfda_docs/label/2012/050261s101lbl.pdf
unhealthy
Health Status: unhealthy
Sources:
https://www.accessdata.fda.gov/drugsatfda_docs/label/2012/050261s101lbl.pdf
Disc. AE: Diarrhea, Clostridium difficile...
AEs leading to
discontinuation/dose reduction:
Diarrhea, Clostridium difficile (grade 5)
Sources:
https://www.accessdata.fda.gov/drugsatfda_docs/label/2012/050261s101lbl.pdf
AEs

AEs

AESignificanceDosePopulation
Nephrotoxicity Disc. AE
600 mg 4 times / day multiple, oral
Highest studied dose
Dose: 600 mg, 4 times / day
Route: oral
Route: multiple
Dose: 600 mg, 4 times / day
Sources:
https://pubmed.ncbi.nlm.nih.gov/103083/
unhealthy, 64 years
n = 1
Health Status: unhealthy
Condition: meningitis
Age Group: 64 years
Sex: M
Population Size: 1
Sources:
https://pubmed.ncbi.nlm.nih.gov/103083/
Fetal damage grade 5
Disc. AE
150 mg 4 times / day multiple, oral
Dose: 150 mg, 4 times / day
Route: oral
Route: multiple
Dose: 150 mg, 4 times / day
Sources:
https://www.accessdata.fda.gov/drugsatfda_docs/label/2012/050261s101lbl.pdf
pregnant
Health Status: pregnant
Sex: F
Sources:
https://www.accessdata.fda.gov/drugsatfda_docs/label/2012/050261s101lbl.pdf
Diarrhea, Clostridium difficile grade 5
Disc. AE
150 mg 4 times / day multiple, oral
Dose: 150 mg, 4 times / day
Route: oral
Route: multiple
Dose: 150 mg, 4 times / day
Sources:
https://www.accessdata.fda.gov/drugsatfda_docs/label/2012/050261s101lbl.pdf
unhealthy
Health Status: unhealthy
Sources:
https://www.accessdata.fda.gov/drugsatfda_docs/label/2012/050261s101lbl.pdf
Overview

Overview

CYP3A4CYP2C9CYP2D6hERG

OverviewOther

Other InhibitorOther SubstrateOther Inducer
OAT3
642
Drug as perpetrator​

Drug as perpetrator​

TargetModalityActivityMetaboliteClinical evidence
OAT3
644
 yes
Sourcing

Sourcing

Vendor/AggregatorIDURL
ChEBI
CHEBI:4392
https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:4392
ZINC
ZINC000100036924
http://zinc15.docking.org/substances/ZINC000100036924
eMolecules
32176309
https://www.emolecules.com/cgi-bin/more?vid=32176309
PubMed

PubMed

TitleDatePubMed
Nephrotoxicity of demethylchlortetracycline hydrochloride. A prospective study.
1967 Oct
Renal failure associated with demeclocycline in cirrhosis.
1977 Aug
Demeclocycline-induced phosphate diabetes in patients with inappropriate secretion of antidiuretic hormone.
1985 Dec 5
Demeclocycline-induced phosphate diabetes in a patient with inappropriate ADH secretion and systemic sarcoidosis.
1993
Irreversible nephrotoxicity from demeclocycline in the treatment of hyponatremia.
2002 Mar
Patents

Patents

JP2003510349A
4
JP2011528275A
455

Sample Use Guides

In Vivo Use Guide
Therapy should be continued for at least 24 to 48 hours after symptoms and fever have subsided. Concomitant therapy: Absorption of tetracyclines is impaired by antacids containing aluminum, calcium, or magnesium, and by iron-containing preparations. Foods and some dairy products also interfere with absorption. Oral forms of tetracycline should be given at least 1 hour before or 2 hours after meals. In patients with renal impairment: Tetracyclines should be used cautiously in patients with impaired renal function. Total dosage should be decreased by reduction of recommended individual doses and/or by extending time intervals between doses. In patients with liver impairment: Tetracyclines should be used cautiously in patients with impaired liver function. Total dosage should be decreased by reduction of recommended individual doses and/or by extending time intervals between doses. Administration of adequate amounts of fluid with the oral formulations of tetracyclines is recommended to wash down the drugs and reduce the risk of esophageal irritation and ulceration. Adults: Usual daily dose – Four divided doses of 150 mg each or two divided doses of 300 mg each. For pediatric patients above eight years of age: Usual daily dose, 7 to 13 mg per kg body weight per day, depending upon the severity of the disease, divided into two to four doses not to exceed adult dosage of 600 mg per day. Gonorrhea patients sensitive to penicillin may be treated with demeclocycline administered as an initial oral dose of 600 mg followed by 300 mg every 12 hours for four days to a total of 3 grams.
Route of Administration: Oral
In Vitro Use Guide
Demeclocycline protects cultured cerebellar granule neurons against glutamate toxicity at doses ranging between 80 and 150 μM.
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:06:51 GMT 2023
Edited
by admin
on Fri Dec 15 15:06:51 GMT 2023
Record UNII
29O079NTYT
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DEMECLOCYCLINE HYDROCHLORIDE
EP   MART.   MI   ORANGE BOOK   USP   USP-RS   VANDF   WHO-DD  
Common Name English
DEMECLOCYCLINE HCL
Common Name English
DEMETHYLCHLORTETRACYCLINE HYDROCHLORIDE [JAN]
Common Name English
DEMECLOCYCLINE HYDROCHLORIDE [MART.]
Common Name English
Demeclocycline hydrochloride [WHO-DD]
Common Name English
DECLOSTATIN
Brand Name English
NSC-756708
Code English
LEDERMYCIN
Brand Name English
DEMECLOCYCLINE HYDROCHLORIDE [USP MONOGRAPH]
Common Name English
7-Chloro-4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,6,10,12,12a-pentahydroxy-1,11-dioxo-2-naphthacenecarboxamide monohydrochloride
Common Name English
DEMECLOCYCLINE HYDROCHLORIDE [EP MONOGRAPH]
Common Name English
2-NAPHTHACENECARBOXAMIDE, 7-CHLORO-4-(DIMETHYLAMINO)-1,4,4A,5,5A,6,11,12A-OCTAHYDRO-3,6,10,12,12A-PENTAHYDROXY-1,11-DIOXO-, MONOHYDROCHLORIDE, (4S-(4.ALPHA.,4A.ALPHA.,5A.ALPHA.,6.BETA.,12A.ALPHA.))-
Common Name English
DEMECLOCYCLINE HYDROCHLORIDE [VANDF]
Common Name English
DEMECLOCYCLINE HYDROCHLORIDE [ORANGE BOOK]
Common Name English
DEMECLOCYCLINE HYDROCHLORIDE [MI]
Common Name English
DECLOMYCIN
Brand Name English
DEMETHYLCHLORTETRACYCLINE HYDROCHLORIDE
Common Name English
DEMECLOCYCLINE HYDROCHLORIDE [USP-RS]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C1595
Created by admin on Fri Dec 15 15:06:51 GMT 2023 , Edited by admin on Fri Dec 15 15:06:51 GMT 2023
Code System Code Type Description
DAILYMED
29O079NTYT
Created by admin on Fri Dec 15 15:06:51 GMT 2023 , Edited by admin on Fri Dec 15 15:06:51 GMT 2023
PRIMARY
EPA CompTox
DTXSID0045252
Created by admin on Fri Dec 15 15:06:51 GMT 2023 , Edited by admin on Fri Dec 15 15:06:51 GMT 2023
PRIMARY
EVMPD
SUB01578MIG
Created by admin on Fri Dec 15 15:06:51 GMT 2023 , Edited by admin on Fri Dec 15 15:06:51 GMT 2023
PRIMARY
NCI_THESAURUS
C28975
Created by admin on Fri Dec 15 15:06:51 GMT 2023 , Edited by admin on Fri Dec 15 15:06:51 GMT 2023
PRIMARY
ChEMBL
CHEMBL1591
Created by admin on Fri Dec 15 15:06:51 GMT 2023 , Edited by admin on Fri Dec 15 15:06:51 GMT 2023
PRIMARY
RXCUI
81993
Created by admin on Fri Dec 15 15:06:51 GMT 2023 , Edited by admin on Fri Dec 15 15:06:51 GMT 2023
PRIMARY RxNorm
RS_ITEM_NUM
1170000
Created by admin on Fri Dec 15 15:06:51 GMT 2023 , Edited by admin on Fri Dec 15 15:06:51 GMT 2023
PRIMARY
MERCK INDEX
m4160
Created by admin on Fri Dec 15 15:06:51 GMT 2023 , Edited by admin on Fri Dec 15 15:06:51 GMT 2023
PRIMARY Merck Index
DRUG BANK
DBSALT000040
Created by admin on Fri Dec 15 15:06:51 GMT 2023 , Edited by admin on Fri Dec 15 15:06:51 GMT 2023
PRIMARY
SMS_ID
100000088394
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PRIMARY
CAS
64-73-3
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PRIMARY
ECHA (EC/EINECS)
200-592-2
Created by admin on Fri Dec 15 15:06:51 GMT 2023 , Edited by admin on Fri Dec 15 15:06:51 GMT 2023
PRIMARY
CHEBI
59725
Created by admin on Fri Dec 15 15:06:51 GMT 2023 , Edited by admin on Fri Dec 15 15:06:51 GMT 2023
PRIMARY
FDA UNII
29O079NTYT
Created by admin on Fri Dec 15 15:06:51 GMT 2023 , Edited by admin on Fri Dec 15 15:06:51 GMT 2023
PRIMARY
NSC
756708
Created by admin on Fri Dec 15 15:06:51 GMT 2023 , Edited by admin on Fri Dec 15 15:06:51 GMT 2023
PRIMARY
Related Record Type Details
Structure of DEMECLOCYCLINE
PARENT -> SALT/SOLVATE
Related Record Type Details
Structure of DEMECLOCYCLINE
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