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Details

Stereochemistry ACHIRAL
Molecular Formula C15H10NO3.Na
Molecular Weight 275.2346
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CRIDANIMOD SODIUM

SMILES

[Na+].[O-]C(=O)CN1C2=C(C=CC=C2)C(=O)C3=C1C=CC=C3

InChI

InChIKey=FQMLTEAEJZVTAJ-UHFFFAOYSA-M
InChI=1S/C15H11NO3.Na/c17-14(18)9-16-12-7-3-1-5-10(12)15(19)11-6-2-4-8-13(11)16;/h1-8H,9H2,(H,17,18);/q;+1/p-1

HIDE SMILES / InChI

Molecular Formula Na
Molecular Weight 22.9898
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C15H10NO3
Molecular Weight 252.2448
Charge -1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: The description was created based on several sources, including https://clinicaltrials.gov/ct2/show/NCT02064725 | https://clinicaltrials.gov/ct2/show/NCT03077698

Cridanimod (Virexxa) is a small-molecule immunomodulator and interferon inducer, which, in preliminary studies, has been shown to increase progesterone receptor expression in endometrial tissue. Restoration of progesterone receptor expression may re-sensitize endometrial tumor tissue to progestin therapy in previously unresponsive tumors. Cridanimod was originally developed by Polysan and Pharmsynthez and licensed to Xenetic Biosciences. Virexxa is currently being studied in an ongoing Phase 2 multi-national study in conjunction with progestin therapy for the treatment of endometrial cancer in women with the recurrent or persistent disease who have failed progestin monotherapy.

Originator

Sources: Berichte der Deutschen Chemischen Gesellschaft [Abteilung] B: Abhandlungen (1923), 56B, 1828-31.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
HIV-1 neutralization and tumor cell proliferation inhibition in vitro by simplified analogues of pyrido[4,3,2-mn]thiazolo[5,4-b]acridine marine alkaloids.
1992 Jul 24
[Increase in NK-activity using superlow doses of the immunomodulator cycloferon].
2001
Correlations between in vitro effects of preparations of interferon and its inducers on blood cells in patients with multiple sclerosis.
2001 Apr
[Effect of interferon inductors on infection induced by hepatitis C virus and activity of mRNA cytokines in cell cultures SW-13 and MT-4].
2002 Nov-Dec
Direct antiviral effect of cycloferon (10-carboxymethyl-9-acridanone) against adenovirus type 6 in vitro.
2003 Apr
[Use of cycloferon in a combined treatment of chlamydial conjunctivitis].
2003 Jan-Feb
[Neuroimmunopathologic aspects of epilepsy].
2004
[The preclinical diagnosis, prevention and treatment of postoperative iridocyclitis in patients after intraocular aphakia correction].
2004 Jul-Aug
[Cycloferon--a new domestic preparation for the prophylaxis of influenza and other acute respiratory viral infections].
2004 Nov-Dec
[Cyclopheron pretreatment in opisthorchiasis management in patients with viral hepatitis C].
2005
[Influence of cycloferon on the biological properties of bacterial intracellular pathogens].
2005 May-Jun
Structural, spectroscopic, and magnetic study of bis(9,10-dihydro-9-oxo-10-acridineacetate)bis(imidazole)bis(methanol) nickel(II).
2006 Dec 25
[Effect of intranasal aerosol-therapy with cycloferon on the function of respiration in patients with some forms of rhinitis].
2007 Jan
[Cycloferon in the treatment of infectious diseases].
2008
[Immunomodulators in the "gold standard" of the chronic viral hepatitis C therapy].
2008
[Improvement of natural resistance in children for prophylaxis of influenza and acute respiratory tract viral infections (results of multicenter randomized trials)].
2009
[Up-to-date approach to treatment of inflammatory infections in the maxillofacial region].
2009
[Cycloferon efficacy in viral and bacterial diseases of children (clinical review)].
2010
[Optimization of prophylaxis of relapses of primary erysipelas with the use of cyclopheron].
2010
[Use of cycloferon in the treatment of patients with pulmonary tuberculosis with mild clinical manifestations].
2010
[Efficiency of using cycloferon as part of combined therapy for chronic hepatitis C (a review of multicenter clinical trials)].
2010
[The cytokine profile in the acute period of tick-borne neuroinfections in children].
2010
[Clinical laboratory approaches to parodontitis treatment optimization].
2010
[Effectiveness of cycloferon liniment in a complex treatment, and monitoring of cytokine profile of gingival fluid of patients with paradontitis].
2010
[Optimization of parodontitis treatment of patients with tuberculosis].
2010
[Changes of functional activity of peripheral blood leukocytes during the immunotherapy of tick-borne infections in children].
2010
[Cycloferon in complex therapy of chronic brucellosis].
2010
[The use of cycloferon in the combined treatment of tuberculosis patients infected with HIV and viral hepatitis].
2010
[Correction of immunity disorders, treatment of intestinal infections and disbiosis in children (clinical review)].
2010
[Pathogenetically substantiated therapy of patients with virus hepatitis C, quality of life, and the disease outcome risk (clinical survey)].
2010
[Efficacy of cycloferon in the treatment of brucellosis].
2010
[Use of immunomodulators in the therapy of chronic hepatitis C: improving standard approach].
2010 Apr
[Combined cycloferon treatment of tuberculosis in patients infected with HIV].
2010 Jul
[Focal immunophysiotherapy in combined treatment of men with manifestations of papilloma virus infection].
2010 Nov-Dec
Patents

Patents

Sample Use Guides

Eligible patients will be enrolled into the study and administered sodium cridanimod (500 mg i.m./ twice a week) in combination with megestrol acetate (160 mg p.o./ day) or medroxyprogesterone acetate (200 mg p.o./ day).
Route of Administration: Intramuscular
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:48:47 GMT 2023
Edited
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on Fri Dec 15 17:48:47 GMT 2023
Record UNII
54W868ROLR
Record Status Validated (UNII)
Record Version
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Name Type Language
CRIDANIMOD SODIUM
Common Name English
Cridanimod sodium [WHO-DD]
Common Name English
NEOVIR
Brand Name English
SODIUM 9-OXO-10-ACRIDINEACETATE
Systematic Name English
XBIO-101
Code English
CAMEDONE
Common Name English
10(9H)-ACRIDINEACETIC ACID, 9-OXO-, SODIUM SALT (1:1)
Common Name English
CAMEDON
WHO-DD  
Common Name English
Camedon [WHO-DD]
Common Name English
Camedon sodium [WHO-DD]
Common Name English
N-(CARBOXYMETHYL)-9-ACRIDONE SODIUM SALT
Common Name English
Classification Tree Code System Code
FDA ORPHAN DRUG 267508
Created by admin on Fri Dec 15 17:48:47 GMT 2023 , Edited by admin on Fri Dec 15 17:48:47 GMT 2023
NCI_THESAURUS C2140
Created by admin on Fri Dec 15 17:48:47 GMT 2023 , Edited by admin on Fri Dec 15 17:48:47 GMT 2023
NCI_THESAURUS C308
Created by admin on Fri Dec 15 17:48:47 GMT 2023 , Edited by admin on Fri Dec 15 17:48:47 GMT 2023
Code System Code Type Description
NCI_THESAURUS
C114298
Created by admin on Fri Dec 15 17:48:47 GMT 2023 , Edited by admin on Fri Dec 15 17:48:47 GMT 2023
PRIMARY
CAS
58880-43-6
Created by admin on Fri Dec 15 17:48:47 GMT 2023 , Edited by admin on Fri Dec 15 17:48:47 GMT 2023
PRIMARY
EPA CompTox
DTXSID10932383
Created by admin on Fri Dec 15 17:48:47 GMT 2023 , Edited by admin on Fri Dec 15 17:48:47 GMT 2023
PRIMARY
SMS_ID
100000076618
Created by admin on Fri Dec 15 17:48:47 GMT 2023 , Edited by admin on Fri Dec 15 17:48:47 GMT 2023
PRIMARY
EVMPD
SUB13209MIG
Created by admin on Fri Dec 15 17:48:47 GMT 2023 , Edited by admin on Fri Dec 15 17:48:47 GMT 2023
PRIMARY
FDA UNII
54W868ROLR
Created by admin on Fri Dec 15 17:48:47 GMT 2023 , Edited by admin on Fri Dec 15 17:48:47 GMT 2023
PRIMARY
PUBCHEM
23684339
Created by admin on Fri Dec 15 17:48:47 GMT 2023 , Edited by admin on Fri Dec 15 17:48:47 GMT 2023
PRIMARY
CAS
144696-36-6
Created by admin on Fri Dec 15 17:48:47 GMT 2023 , Edited by admin on Fri Dec 15 17:48:47 GMT 2023
SUPERSEDED
CAS
351531-53-8
Created by admin on Fri Dec 15 17:48:47 GMT 2023 , Edited by admin on Fri Dec 15 17:48:47 GMT 2023
SUPERSEDED
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