U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C24H30N2O8
Molecular Weight 474.5036
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MITOPODOZIDE

SMILES

CCNNC(=O)[C@H]1[C@H](CO)[C@@H](O)C2=C(C=C3OCOC3=C2)[C@H]1C4=CC(OC)=C(OC)C(OC)=C4

InChI

InChIKey=CPTIBDHUFVHUJK-NZYDNVMFSA-N
InChI=1S/C24H30N2O8/c1-5-25-26-24(29)21-15(10-27)22(28)14-9-17-16(33-11-34-17)8-13(14)20(21)12-6-18(30-2)23(32-4)19(7-12)31-3/h6-9,15,20-22,25,27-28H,5,10-11H2,1-4H3,(H,26,29)/t15-,20+,21-,22-/m0/s1

HIDE SMILES / InChI

Molecular Formula C24H30N2O8
Molecular Weight 474.5036
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Mitopodozide (“Proresid') is a cytotoxic drug, also of natural origin, being derived from the root of an American plant of the podophyllum family. Proresid has also been used as a disease-modifying antirheumatic drug since the late 1960s. Proresid is a microtubulin antagonist comparable to colchicine and griseofulvin. It has antimitotic and granulocytechemotaxis-inhibiting properties. Proresid has been used with good results as a disease-modifying drug (DMD) in the treatment of Rheumatoid Arthritis (RA). A high frequency of gastrointestinal side effects, mostly diarrhoea is reported. Initially, Proresid was used as an anticancer agent, but it was later discovered that his anti-tumor effect is limited in comparison with other cytostatics, and its use for this purpose has therefore been discontinued. Later it was discovered that Proresid may be used in the treatment of rheumatoid arthritis and rare cases of secondary amyloidosis. However, the gastrointestinal tract side effects have made it impossible to use Proresid in doses high enough to provide really useful therapeutic effect.

Approval Year

PubMed

PubMed

TitleDatePubMed
Patents

Patents

Sample Use Guides

Rheumatoid arthritis: the starting dose of Proresid, dispensed as 50 mg capsules, was 100 mg/day. The dose was increased weekly until a maintenance dose of 200-300 mg/day was achieved.
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Sat Dec 16 16:54:43 GMT 2023
Edited
by admin
on Sat Dec 16 16:54:43 GMT 2023
Record UNII
6QYI7Y8OBO
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MITOPODOZIDE
INN   WHO-DD  
INN  
Official Name English
mitopodozide [INN]
Common Name English
PODOPHYLLIC ACIDS TRANS-2-ETHYLHYDRAZIDE
MI  
Common Name English
SPI-77
Code English
Mitopodozide [WHO-DD]
Common Name English
NSC-72274
Code English
PODOPHYLLIC ACID 2-ETHYLHYDRAZIDE
Common Name English
PODOPHYLLIC ACIDS TRANS-2-ETHYLHYDRAZIDE [MI]
Common Name English
Code System Code Type Description
ECHA (EC/EINECS)
216-138-1
Created by admin on Sat Dec 16 16:54:43 GMT 2023 , Edited by admin on Sat Dec 16 16:54:43 GMT 2023
PRIMARY
EVMPD
SUB09008MIG
Created by admin on Sat Dec 16 16:54:43 GMT 2023 , Edited by admin on Sat Dec 16 16:54:43 GMT 2023
PRIMARY
EPA CompTox
DTXSID9021211
Created by admin on Sat Dec 16 16:54:43 GMT 2023 , Edited by admin on Sat Dec 16 16:54:43 GMT 2023
PRIMARY
MERCK INDEX
m8932
Created by admin on Sat Dec 16 16:54:43 GMT 2023 , Edited by admin on Sat Dec 16 16:54:43 GMT 2023
PRIMARY Merck Index
FDA UNII
6QYI7Y8OBO
Created by admin on Sat Dec 16 16:54:43 GMT 2023 , Edited by admin on Sat Dec 16 16:54:43 GMT 2023
PRIMARY
PUBCHEM
251643
Created by admin on Sat Dec 16 16:54:43 GMT 2023 , Edited by admin on Sat Dec 16 16:54:43 GMT 2023
PRIMARY
NCI_THESAURUS
C166959
Created by admin on Sat Dec 16 16:54:43 GMT 2023 , Edited by admin on Sat Dec 16 16:54:43 GMT 2023
PRIMARY
DRUG CENTRAL
2312
Created by admin on Sat Dec 16 16:54:43 GMT 2023 , Edited by admin on Sat Dec 16 16:54:43 GMT 2023
PRIMARY
INN
2221
Created by admin on Sat Dec 16 16:54:43 GMT 2023 , Edited by admin on Sat Dec 16 16:54:43 GMT 2023
PRIMARY
MESH
C003170
Created by admin on Sat Dec 16 16:54:43 GMT 2023 , Edited by admin on Sat Dec 16 16:54:43 GMT 2023
PRIMARY
SMS_ID
100000080899
Created by admin on Sat Dec 16 16:54:43 GMT 2023 , Edited by admin on Sat Dec 16 16:54:43 GMT 2023
PRIMARY
CAS
1508-45-8
Created by admin on Sat Dec 16 16:54:43 GMT 2023 , Edited by admin on Sat Dec 16 16:54:43 GMT 2023
PRIMARY
NSC
72274
Created by admin on Sat Dec 16 16:54:43 GMT 2023 , Edited by admin on Sat Dec 16 16:54:43 GMT 2023
PRIMARY
ChEMBL
CHEMBL1908339
Created by admin on Sat Dec 16 16:54:43 GMT 2023 , Edited by admin on Sat Dec 16 16:54:43 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY