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

Details

Stereochemistry RACEMIC
Molecular Formula C18H31N4O9.Gd
Molecular Weight 604.71
Optical Activity ( + / - )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GADOBUTROL

SMILES

[Gd+3].OC[C@@H](O)[C@@H](CO)N1CCN(CC([O-])=O)CCN(CC([O-])=O)CCN(CC([O-])=O)CC1

InChI

InChIKey=ZPDFIIGFYAHNSK-CTHHTMFSSA-K
InChI=1S/C18H34N4O9.Gd/c23-12-14(15(25)13-24)22-7-5-20(10-17(28)29)3-1-19(9-16(26)27)2-4-21(6-8-22)11-18(30)31;/h14-15,23-25H,1-13H2,(H,26,27)(H,28,29)(H,30,31);/q;+3/p-3/t14-,15-;/m1./s1

HIDE SMILES / InChI

Molecular Formula C18H31N4O9
Molecular Weight 447.4601
Charge -3
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Molecular Formula Gd
Molecular Weight 157.25
Charge 3
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/7960618; https://www.ncbi.nlm.nih.gov/pubmed/?term=23435930; http://mnoncology.com/disease-drug-info/drug-dictionary/G/

DOTAREM (Gadoterate Meglumine ) is a gadolinium-based contrast agent indicated for intravenous use with magnetic resonance imaging (MRI) in brain (intracranial), spine and associatedtissues in adult and pediatric patients (2 years of age and older) to detect and visualize areas with disruption of the blood brain barrier (BBB) and/or abnormal vascularity. Gadoterate Meglumine is a gadolinium chelate paramagnetic contrast agent. When placed in a magnetic field, gadoterate meglumine produces a large magnetic moment and so a large local magnetic field, which can enhance the relaxation rate of nearby protons; as a result, the signal intensity of tissue images observed with magnetic resonance imaging (MRI) may be enhanced. Because this agent is preferentially taken up by normal functioning hepatocytes, normal hepatic tissue is enhanced with MRI while tumor tissue is unenhanced. In addition, because gadobenate dimeglumine is excreted in the bile, it may be used to visualize the biliary system using MRI.

CNS Activity

Curator's Comment: Gadoterate does not cross the intact blood-brain barrier and, therefore, does not enhance normal brain or lesions that have a normal blood-brain barrier, e.g. cysts, mature post-operative scars. However, disruption of the bloodbrain barrier or abnormal vascularity allows distribution of gadoterate in lesions such as neoplasms, abscesses, and infarcts.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P27169
Gene ID: 5444.0
Gene Symbol: PON1
Target Organism: Homo sapiens (Human)
105.0 mM [Ki]
Target ID: P52209
Gene ID: 5226.0
Gene Symbol: PGD
Target Organism: Homo sapiens (Human)
73.0 mM [Ki]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Diagnostic
DOTAREM

Approved Use

Indicated for intravenous use with magnetic resonance imaging (MRI) in brain (intracranial), spine and associated tissues in adult and pediatric patients (2 years of age and older) to detect and visualize areas with disruption of the blood brain barrier (BBB) and/or abnormal vascularity.

Launch Date

2013
Diagnostic
GADAVIST

Approved Use

Gadavist is a gadolinium-based contrast agent indicated for use with magnetic resonance imaging to detect and visualize areas with disrupted blood brain barrier and/or abnormal vascularity of the central nervous system in adult and pediatric patients (including term neonates); to assess the presence and extent of malignant breast disease; to evaluate known or suspected supra-aortic or renal artery disease in adult and pediatric patients (including term neonates) disease.

Launch Date

2011
Diagnostic
GADAVIST

Approved Use

Gadavist is a gadolinium-based contrast agent indicated for use with magnetic resonance imaging to detect and visualize areas with disrupted blood brain barrier and/or abnormal vascularity of the central nervous system in adult and pediatric patients (including term neonates); to assess the presence and extent of malignant breast disease; to evaluate known or suspected supra-aortic or renal artery disease in adult and pediatric patients (including term neonates) disease.

Launch Date

2011
Diagnostic
GADAVIST

Approved Use

Gadavist is a gadolinium-based contrast agent indicated for use with magnetic resonance imaging to detect and visualize areas with disrupted blood brain barrier and/or abnormal vascularity of the central nervous system in adult and pediatric patients (including term neonates); to assess the presence and extent of malignant breast disease; to evaluate known or suspected supra-aortic or renal artery disease in adult and pediatric patients (including term neonates) disease.

Launch Date

2011
PubMed

PubMed

TitleDatePubMed
The transient receptor potential protein homologue TRP6 is the essential component of vascular alpha(1)-adrenoceptor-activated Ca(2+)-permeable cation channel.
2001 Feb 16
Extracellular calcium-sensing receptor is expressed in rat hepatocytes. coupling to intracellular calcium mobilization and stimulation of bile flow.
2001 Feb 9
Inhibition of transiently expressed low- and high-voltage-activated calcium channels by trivalent metal cations.
2002 Jun 1
Diacylglycerol activates the influx of extracellular cations in T-lymphocytes independently of intracellular calcium-store depletion and possibly involving endogenous TRP6 gene products.
2002 May 15
A novel cation-sensing mechanism in osteoblasts is a molecular target for strontium.
2004 May
Loss of primary cilia results in deregulated and unabated apical calcium entry in ARPKD collecting duct cells.
2006 Jun
Metabotropic receptor-activated calcium increases and store-operated calcium influx in mouse Müller cells.
2008 Jul
Renal failure and gadolinium. The number of documented cases is rising.
2008 Oct
Persistent activation of dermal fibroblasts from patients with gadolinium-associated nephrogenic systemic fibrosis.
2010 Nov
Tumor Detection at 3 Tesla with an Activatable Cell Penetrating Peptide Dendrimer (ACPPD-Gd), a T1 Magnetic Resonance (MR) Molecular Imaging Agent.
2015
MR Angiography at 3 T of Peripheral Arterial Disease: A Randomized Prospective Comparison of Gadoterate Meglumine and Gadobutrol.
2015 Jun
MRI in multiple sclerosis: an intra-individual, randomized and multicentric comparison of gadobutrol with gadoterate meglumine at 3 T.
2016 Mar
Patents

Sample Use Guides

Recommended dose for adults and pediatric patients (including term neonates) is 0.1 mL/kg body weight. Administer as an intravenous bolus injection. Follow injection with a normal saline flush.
Route of Administration: Intravenous
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:58:59 GMT 2023
Edited
by admin
on Fri Dec 15 16:58:59 GMT 2023
Record UNII
1BJ477IO2L
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GADOBUTROL
DASH   INN   JAN   MART.   MI   ORANGE BOOK   USAN   VANDF   WHO-DD  
USAN   INN  
Official Name English
gadobutrol [INN]
Common Name English
GADOBUTROL [USP-RS]
Common Name English
GADOBUTROL [USAN]
Common Name English
PROTOVIST
Brand Name English
GADOBUTROL [USP MONOGRAPH]
Common Name English
GADOVIST
Common Name English
GADOBUTROL [JAN]
Common Name English
ZK 135079
Code English
ZK-135079
Code English
GADOBUTROL [ORANGE BOOK]
Common Name English
GADOLINIUM, (10-(2,3-DIHYDROXY-1-(HYDROXYMETHYL)PROPYL)-1,4,7,10-TETRAAZACYCLODODECANE-1,4,7-TRIACETATO(3-)-N1,N4,N7,N10,O1,O4,O7)-
Systematic Name English
GADOBUTROL [VANDF]
Common Name English
(10-((1RS,2SR)-2,3-DIHYDROXY-1-(HYDROXYMETHYL)PROPYL)-1,4,7,10-TETRAAZACYCLODODECANE-1,4,7-TRIACETATO(3-)GADOLINIUM
Common Name English
BAY86-4875
Code English
Gadobutrol [WHO-DD]
Common Name English
GADOBUTROL [MI]
Common Name English
GADOGRAF
Brand Name English
GADAVIST
Brand Name English
GADOBUTROL [MART.]
Common Name English
Classification Tree Code System Code
NDF-RT N0000183362
Created by admin on Fri Dec 15 16:58:59 GMT 2023 , Edited by admin on Fri Dec 15 16:58:59 GMT 2023
WHO-ATC V08CA09
Created by admin on Fri Dec 15 16:58:59 GMT 2023 , Edited by admin on Fri Dec 15 16:58:59 GMT 2023
WHO-VATC QV08CA09
Created by admin on Fri Dec 15 16:58:59 GMT 2023 , Edited by admin on Fri Dec 15 16:58:59 GMT 2023
NCI_THESAURUS C62358
Created by admin on Fri Dec 15 16:58:59 GMT 2023 , Edited by admin on Fri Dec 15 16:58:59 GMT 2023
Code System Code Type Description
DAILYMED
1BJ477IO2L
Created by admin on Fri Dec 15 16:58:59 GMT 2023 , Edited by admin on Fri Dec 15 16:58:59 GMT 2023
PRIMARY
DRUG CENTRAL
4179
Created by admin on Fri Dec 15 16:58:59 GMT 2023 , Edited by admin on Fri Dec 15 16:58:59 GMT 2023
PRIMARY
RXCUI
84990
Created by admin on Fri Dec 15 16:58:59 GMT 2023 , Edited by admin on Fri Dec 15 16:58:59 GMT 2023
PRIMARY RxNorm
CHEBI
68841
Created by admin on Fri Dec 15 16:58:59 GMT 2023 , Edited by admin on Fri Dec 15 16:58:59 GMT 2023
PRIMARY
MERCK INDEX
m5623
Created by admin on Fri Dec 15 16:58:59 GMT 2023 , Edited by admin on Fri Dec 15 16:58:59 GMT 2023
PRIMARY Merck Index
NCI_THESAURUS
C70675
Created by admin on Fri Dec 15 16:58:59 GMT 2023 , Edited by admin on Fri Dec 15 16:58:59 GMT 2023
PRIMARY
EVMPD
SUB07861MIG
Created by admin on Fri Dec 15 16:58:59 GMT 2023 , Edited by admin on Fri Dec 15 16:58:59 GMT 2023
PRIMARY
LACTMED
Gadobutrol
Created by admin on Fri Dec 15 16:58:59 GMT 2023 , Edited by admin on Fri Dec 15 16:58:59 GMT 2023
PRIMARY
PUBCHEM
6102852
Created by admin on Fri Dec 15 16:58:59 GMT 2023 , Edited by admin on Fri Dec 15 16:58:59 GMT 2023
PRIMARY
EPA CompTox
DTXSID101027434
Created by admin on Fri Dec 15 16:58:59 GMT 2023 , Edited by admin on Fri Dec 15 16:58:59 GMT 2023
PRIMARY
CAS
138071-82-6
Created by admin on Fri Dec 15 16:58:59 GMT 2023 , Edited by admin on Fri Dec 15 16:58:59 GMT 2023
SUPERSEDED
CAS
770691-21-9
Created by admin on Fri Dec 15 16:58:59 GMT 2023 , Edited by admin on Fri Dec 15 16:58:59 GMT 2023
PRIMARY
ChEMBL
CHEMBL2218860
Created by admin on Fri Dec 15 16:58:59 GMT 2023 , Edited by admin on Fri Dec 15 16:58:59 GMT 2023
PRIMARY
MESH
C090600
Created by admin on Fri Dec 15 16:58:59 GMT 2023 , Edited by admin on Fri Dec 15 16:58:59 GMT 2023
PRIMARY
RS_ITEM_NUM
1287449
Created by admin on Fri Dec 15 16:58:59 GMT 2023 , Edited by admin on Fri Dec 15 16:58:59 GMT 2023
PRIMARY
WIKIPEDIA
GADOBUTROL
Created by admin on Fri Dec 15 16:58:59 GMT 2023 , Edited by admin on Fri Dec 15 16:58:59 GMT 2023
PRIMARY
USAN
XX-91
Created by admin on Fri Dec 15 16:58:59 GMT 2023 , Edited by admin on Fri Dec 15 16:58:59 GMT 2023
PRIMARY
DRUG BANK
DB06703
Created by admin on Fri Dec 15 16:58:59 GMT 2023 , Edited by admin on Fri Dec 15 16:58:59 GMT 2023
PRIMARY
FDA UNII
1BJ477IO2L
Created by admin on Fri Dec 15 16:58:59 GMT 2023 , Edited by admin on Fri Dec 15 16:58:59 GMT 2023
PRIMARY
HSDB
8231
Created by admin on Fri Dec 15 16:58:59 GMT 2023 , Edited by admin on Fri Dec 15 16:58:59 GMT 2023
PRIMARY
SMS_ID
100000092300
Created by admin on Fri Dec 15 16:58:59 GMT 2023 , Edited by admin on Fri Dec 15 16:58:59 GMT 2023
PRIMARY
INN
6882
Created by admin on Fri Dec 15 16:58:59 GMT 2023 , Edited by admin on Fri Dec 15 16:58:59 GMT 2023
PRIMARY
Related Record Type Details
EXCRETED UNCHANGED
The urinary excretion of gadolinium was almost completed after 12 h post injection with a mean recovery between 90.4–99.3 % of the administered gadolinium dose.
URINE
SOLVATE->ANHYDROUS
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY
Name Property Type Amount Referenced Substance Defining Parameters References
Biological Half-life PHARMACOKINETIC a single intravenous administration of gadovist 1.0 M