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Details

Stereochemistry ABSOLUTE
Molecular Formula C33H44N3O14P
Molecular Weight 737.6879
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FOSVESET

SMILES

OC(=O)CN(CCN(CC(O)=O)CC(O)=O)C[C@H](COP(O)(=O)OC1CCC(CC1)(C2=CC=CC=C2)C3=CC=CC=C3)N(CC(O)=O)CC(O)=O

InChI

InChIKey=NZLPWFTXPYJYSS-AREMUKBSSA-N
InChI=1S/C33H44N3O14P/c37-28(38)18-34(15-16-35(19-29(39)40)20-30(41)42)17-26(36(21-31(43)44)22-32(45)46)23-49-51(47,48)50-27-11-13-33(14-12-27,24-7-3-1-4-8-24)25-9-5-2-6-10-25/h1-10,26-27H,11-23H2,(H,37,38)(H,39,40)(H,41,42)(H,43,44)(H,45,46)(H,47,48)/t26-/m1/s1

HIDE SMILES / InChI

Molecular Formula C33H44N3O14P
Molecular Weight 737.6879
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Description
Curator's Comment: description was created based on several sources, including: http://radiopaedia.org/articles/gadofosveset-trisodium-1

Gadofosveset trisodium is an intravenous contrast agent used with magnetic resonance angiography (MRA), which is a non-invasive way of imaging blood vessels. The agent allows for the vascular system to be imaged more clearly by the MRA. In this way, gadofosveset trisodium is used to help diagnose certain disorders of the heart and blood vessels. Gadofosveset binds reversibly to endogenous serum albumin resulting in longer vascular residence time than non-protein binding contrast agents. The binding to serum albumin also increases the magnetic resonance relaxivity of gadofosveset and decreases the relaxation time (Tl) of water protons resulting in an increase in signal intensity (brightness) of blood. The extended acquisition time and increased relaxivity of gadofosveset allows for longer steady-state acquisition times, and potentially submillimeter voxels. Overlay of veins in steady-state MR angiography is less of a problem in multiplanar reformats with this level of resolution. This is particularly promising for MR evaluation of the peripheral vasculature. In the United States, gadofosveset is FDA-approved only for use in aortoiliac disease, with other uses being off-label. It currently does not have a role in hepatic imaging.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P02768|||Q86YG0
Gene ID: 213.0
Gene Symbol: ALB
Target Organism: Homo sapiens (Human)
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Diagnostic
ABLAVAR

Approved Use

ABLAVAR Injection is a gadolinium-based contrast agent indicated for use as a contrast agent in magnetic resonance angiography (MRA) to evaluate aortoiliac occlusive disease (AIOD) in adults with known or suspected peripheral vascular disease.

Launch Date

2008
PubMed

PubMed

TitleDatePubMed
Gadolinium contrast agents for CNS imaging: current concepts and clinical evidence.
2014 Dec
Patents

Sample Use Guides

Administer ABLAVAR (gadofosveset trisodium) Injection by an intravenous bolus, manually or by power injection, at a dose of 0.12 mL/kg body weight (0.03 mmol/kg) over a period of time up to 30 seconds followed by a 25-30 mL normal saline flush.
Route of Administration: Intravenous
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:52:04 GMT 2023
Edited
by admin
on Fri Dec 15 15:52:04 GMT 2023
Record UNII
5WBR90FN3H
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FOSVESET
INN   USAN   VANDF  
INN   USAN  
Official Name English
FOSVESET [USAN]
Common Name English
MS325168A
Code English
fosveset [INN]
Common Name English
N-[2-[Bis(carboxymethyl)amino]ethyl]-N-[(R)-2-[bis(carboxymethyl)amino]-3-hydroxypropyl]glycine, 4,4-diphenylcyclohexyl hydrogen phosphate (ester)
Systematic Name English
2-OXA-6,9-DIAZA-1-PHOSPHAUNDECAN-11-OIC ACID, 4-(BIS(CARBOXYMETHYL)AMINO)-6,9-BIS(CARBOXYMETHYL)-1-((4,4-DIPHENYLCYCLOHEXYL)OXY)-1-HYDROXY-, 1-OXIDE
Common Name English
MS-325168A
Code English
FOSVESET [VANDF]
Common Name English
Code System Code Type Description
SMS_ID
100000087355
Created by admin on Fri Dec 15 15:52:04 GMT 2023 , Edited by admin on Fri Dec 15 15:52:04 GMT 2023
PRIMARY
INN
8022
Created by admin on Fri Dec 15 15:52:04 GMT 2023 , Edited by admin on Fri Dec 15 15:52:04 GMT 2023
PRIMARY
EPA CompTox
DTXSID701027787
Created by admin on Fri Dec 15 15:52:04 GMT 2023 , Edited by admin on Fri Dec 15 15:52:04 GMT 2023
PRIMARY
FDA UNII
5WBR90FN3H
Created by admin on Fri Dec 15 15:52:04 GMT 2023 , Edited by admin on Fri Dec 15 15:52:04 GMT 2023
PRIMARY
CAS
193901-91-6
Created by admin on Fri Dec 15 15:52:04 GMT 2023 , Edited by admin on Fri Dec 15 15:52:04 GMT 2023
PRIMARY
EVMPD
SUB21052
Created by admin on Fri Dec 15 15:52:04 GMT 2023 , Edited by admin on Fri Dec 15 15:52:04 GMT 2023
PRIMARY
ChEMBL
CHEMBL1615469
Created by admin on Fri Dec 15 15:52:04 GMT 2023 , Edited by admin on Fri Dec 15 15:52:04 GMT 2023
PRIMARY
NCI_THESAURUS
C166867
Created by admin on Fri Dec 15 15:52:04 GMT 2023 , Edited by admin on Fri Dec 15 15:52:04 GMT 2023
PRIMARY
RXCUI
1312592
Created by admin on Fri Dec 15 15:52:04 GMT 2023 , Edited by admin on Fri Dec 15 15:52:04 GMT 2023
PRIMARY RxNorm
PUBCHEM
158441
Created by admin on Fri Dec 15 15:52:04 GMT 2023 , Edited by admin on Fri Dec 15 15:52:04 GMT 2023
PRIMARY
USAN
KK-105
Created by admin on Fri Dec 15 15:52:04 GMT 2023 , Edited by admin on Fri Dec 15 15:52:04 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
TARGET->LIGAND
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY