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Details

Stereochemistry ACHIRAL
Molecular Formula C22H32N4O14P2
Molecular Weight 638.4554
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FODIPIR

SMILES

CC1=NC=C(COP(O)(O)=O)C(CN(CCN(CC(O)=O)CC2=C(O)C(C)=NC=C2COP(O)(O)=O)CC(O)=O)=C1O

InChI

InChIKey=SQKUFYLUXROIFM-UHFFFAOYSA-N
InChI=1S/C22H32N4O14P2/c1-13-21(31)17(15(5-23-13)11-39-41(33,34)35)7-25(9-19(27)28)3-4-26(10-20(29)30)8-18-16(12-40-42(36,37)38)6-24-14(2)22(18)32/h5-6,31-32H,3-4,7-12H2,1-2H3,(H,27,28)(H,29,30)(H2,33,34,35)(H2,36,37,38)

HIDE SMILES / InChI

Molecular Formula C22H32N4O14P2
Molecular Weight 638.4554
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Volumetric MR imaging of the liver and applications.
2001 Nov
Detection of malignant primary hepatic neoplasms with gadobenate dimeglumine (Gd-BOPTA) enhanced T1-weighted hepatocyte phase MR imaging: results of off-site blinded review in a phase-II multicenter trial.
2001 Oct-Dec
Contrast-enhanced magnetic resonance cholangiography using mangafodipir compared with standard T2W MRC sequences: a pictorial essay.
2004 Aug
Detection and characterization of focal hepatic lesions: mangafodipir vs. superparamagnetic iron oxide-enhanced magnetic resonance imaging.
2004 Oct
Magnetic resonance with manganese-DPDP (mangafodipir) of focal solid pancreatic lesions.
2004 Sep
Characterization of hepatocellular tumors: value of mangafodipir-enhanced magnetic resonance imaging.
2005 Mar-Apr
Ultrasound of living donor liver transplantation.
2006 Apr
Improvement of the therapeutic index of anticancer drugs by the superoxide dismutase mimic mangafodipir.
2006 Feb 15
The magnetic resonance imaging contrast agent mangafodipir exerts antitumor activity via a previously described superoxide dismutase mimetic activity.
2006 Jan 1
MR contrast agents for liver imaging: what, when, how.
2006 Nov-Dec
Characterization of focal liver lesions: use of mangafodipir trisodium (MnDPDP)-enhanced MR images.
2006 Sep
Value of manganese-enhanced T1- and T2-weighted MR cholangiography for differentiating cystic parenchymal lesions from cystic abnormalities which communicate with bile ducts.
2007 Dec 31
[Contrast-enhanced magnetic resonance cholangiography using gadolinium-EOB-DTPA. Preliminary experience and clinical applications].
2007 Jun
Mangafodipir as a cytoprotective adjunct to chemotherapy--a case report.
2009
Pharmacokinetic-pharmacodynamic modeling of manganese after a single intravenous infusion of mangafodipir in patients with acute alcoholic hepatitis.
2009 Oct
Prevention of 7β-hydroxycholesterol-induced cell death by mangafodipir is mediated through lysosomal and mitochondrial pathways.
2010 Aug 25
Patents

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:28:42 GMT 2023
Edited
by admin
on Fri Dec 15 15:28:42 GMT 2023
Record UNII
P28BIW0UTB
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FODIPIR
INN   USAN  
INN   USAN  
Official Name English
FODIPIR [USAN]
Common Name English
DPDP
Code English
fodipir [INN]
Common Name English
GLYCINE, N,N'-1,2-ETHANEDIYLBIS(N-((3-HYDROXY-2-METHYL-5-((PHOSPHONOOXY)METHYL)-4-PYRIDINYL)METHYL)-
Systematic Name English
N,N'-1,2-ETHANEDIYLBIS(N-((3-HYDROXY-2-METHYL-5-((PHOSPHONOOXY)METHYL)-4-PYRIDINYL)METHYL)GLYCINE)
Systematic Name English
Code System Code Type Description
EVMPD
SUB07772MIG
Created by admin on Fri Dec 15 15:28:42 GMT 2023 , Edited by admin on Fri Dec 15 15:28:42 GMT 2023
PRIMARY
SMS_ID
100000080409
Created by admin on Fri Dec 15 15:28:42 GMT 2023 , Edited by admin on Fri Dec 15 15:28:42 GMT 2023
PRIMARY
EPA CompTox
DTXSID1043960
Created by admin on Fri Dec 15 15:28:42 GMT 2023 , Edited by admin on Fri Dec 15 15:28:42 GMT 2023
PRIMARY
FDA UNII
P28BIW0UTB
Created by admin on Fri Dec 15 15:28:42 GMT 2023 , Edited by admin on Fri Dec 15 15:28:42 GMT 2023
PRIMARY
INN
7331
Created by admin on Fri Dec 15 15:28:42 GMT 2023 , Edited by admin on Fri Dec 15 15:28:42 GMT 2023
PRIMARY
PUBCHEM
60683
Created by admin on Fri Dec 15 15:28:42 GMT 2023 , Edited by admin on Fri Dec 15 15:28:42 GMT 2023
PRIMARY
NCI_THESAURUS
C174827
Created by admin on Fri Dec 15 15:28:42 GMT 2023 , Edited by admin on Fri Dec 15 15:28:42 GMT 2023
PRIMARY
USAN
FF-62
Created by admin on Fri Dec 15 15:28:42 GMT 2023 , Edited by admin on Fri Dec 15 15:28:42 GMT 2023
PRIMARY
MESH
C060076
Created by admin on Fri Dec 15 15:28:42 GMT 2023 , Edited by admin on Fri Dec 15 15:28:42 GMT 2023
PRIMARY
CAS
118248-91-2
Created by admin on Fri Dec 15 15:28:42 GMT 2023 , Edited by admin on Fri Dec 15 15:28:42 GMT 2023
PRIMARY
ChEMBL
CHEMBL1208640
Created by admin on Fri Dec 15 15:28:42 GMT 2023 , Edited by admin on Fri Dec 15 15:28:42 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY