Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C17H29N4O7.Gd |
| Molecular Weight | 558.68 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[Gd+3].CC(O)CN1CCN(CC([O-])=O)CCN(CC([O-])=O)CCN(CC([O-])=O)CC1
InChI
InChIKey=DPNNNPAKRZOSMO-UHFFFAOYSA-K
InChI=1S/C17H32N4O7.Gd/c1-14(22)10-18-2-4-19(11-15(23)24)6-8-21(13-17(27)28)9-7-20(5-3-18)12-16(25)26;/h14,22H,2-13H2,1H3,(H,23,24)(H,25,26)(H,27,28);/q;+3/p-3
| 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 |
| Molecular Formula | C17H29N4O7 |
| Molecular Weight | 401.4348 |
| Charge | -3 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
DescriptionCurator's Comment: description was created based on several sources, including:
http://www.drugbank.ca/drugs/DB00597
Curator's Comment: description was created based on several sources, including:
http://www.drugbank.ca/drugs/DB00597
Gadoteridol (INN) is a gadolinium-based MRI contrast agent, used particularly in the imaging of the central nervous system. It is sold under the brand name ProHance. Gadoteridol is a paramagnetic agent and, as such, develops a magnetic moment when placed in a magnetic field. The relatively large magnetic moment produced by the paramagnetic agent results in a relatively large local magnetic field, which can enhance the relaxation rates of water protons in the vicinity of the paramagnetic agent. In magnetic resonance imaging (MRI), visualization of normal and pathologic brain tissue depends in part on variations in the radiofrequency signal intensity that occur with 1) differences in proton density; 2) differences of the spin-lattice or longitudinal relaxation times (T1); and 3) differences in the spin-spin or transverse relaxation time (T2). When placed in a magnetic field, gadoteridol decreases T1 relaxation times in the target tissues. At recommended doses, the effect is observed with greatest sensitivity in the T1-weighted sequences. Gadoteridol does not cross the intact blood-brain barrier and, therefore, does not accumulate in normal brain or in lesions that have a normal blood-brain barrier, e.g., cysts, mature post-operative scars, etc. However, disruption of the blood-brain barrier or abnormal vascularity allows accumulation of gadoteridol in lesions such as neoplasms, abscesses, and subacute infarcts. The pharmacokinetics of ProHance in various lesions is not known.
Approval Year
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Diagnostic | PROHANCE Approved UseGadoteridol Injection is indicated for use in MRI in adults and children over 2 years of age to visualize lesions with abnormal vascularity in the brain (intracranial lesions), spine and associated tissues. Launch Date1993 |
T1/2
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
1.57 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/1506147/ |
0.3 mmol/kg single, intravenous dose: 0.3 mmol/kg route of administration: Intravenous experiment type: SINGLE co-administered: |
GADOTERIDOL serum | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
Overview
| CYP3A4 | CYP2C9 | CYP2D6 | hERG |
|---|---|---|---|
OverviewOther
| Other Inhibitor | Other Substrate | Other Inducer |
|---|---|---|
Tox targets
| Target | Modality | Activity | Metabolite | Clinical evidence |
|---|---|---|---|---|
Sources: https://www.accessdata.fda.gov/drugsatfda_docs/nda/2011/201277Orig1s000PharmR.pdf#page=53 Page: 53.0 |
Sample Use Guides
ADULTS: The recommended dose of (Gadoteridol) Injection is 0.1 mmol/kg (0.2mL/kg) administered as a rapid intravenous infusion (10 mL/min-60 mL/min) or bolus ( >60 mL/min).
CHILDREN (2-18 years): The recommended dose is 0.1 mmol/kg (0.2mL/kg)
administered as a rapid intravenous infusion (10 mL/min-60 mL/min) or bolus (> 60 mL/min).
Route of Administration:
Intravenous
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 06:52:01 GMT 2025
by
admin
on
Wed Apr 02 06:52:01 GMT 2025
|
| Record UNII |
0199MV609F
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Official Name | English | ||
|
Preferred Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
NDF-RT |
N0000175862
Created by
admin on Wed Apr 02 06:52:01 GMT 2025 , Edited by admin on Wed Apr 02 06:52:01 GMT 2025
|
||
|
NDF-RT |
N0000180184
Created by
admin on Wed Apr 02 06:52:01 GMT 2025 , Edited by admin on Wed Apr 02 06:52:01 GMT 2025
|
||
|
WHO-ATC |
V08CA04
Created by
admin on Wed Apr 02 06:52:01 GMT 2025 , Edited by admin on Wed Apr 02 06:52:01 GMT 2025
|
||
|
NCI_THESAURUS |
C62358
Created by
admin on Wed Apr 02 06:52:01 GMT 2025 , Edited by admin on Wed Apr 02 06:52:01 GMT 2025
|
||
|
WHO-VATC |
QV08CA04
Created by
admin on Wed Apr 02 06:52:01 GMT 2025 , Edited by admin on Wed Apr 02 06:52:01 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
GADOTERIDOL
Created by
admin on Wed Apr 02 06:52:01 GMT 2025 , Edited by admin on Wed Apr 02 06:52:01 GMT 2025
|
PRIMARY | |||
|
1268
Created by
admin on Wed Apr 02 06:52:01 GMT 2025 , Edited by admin on Wed Apr 02 06:52:01 GMT 2025
|
PRIMARY | |||
|
120066-54-8
Created by
admin on Wed Apr 02 06:52:01 GMT 2025 , Edited by admin on Wed Apr 02 06:52:01 GMT 2025
|
PRIMARY | |||
|
C062402
Created by
admin on Wed Apr 02 06:52:01 GMT 2025 , Edited by admin on Wed Apr 02 06:52:01 GMT 2025
|
PRIMARY | |||
|
6655
Created by
admin on Wed Apr 02 06:52:01 GMT 2025 , Edited by admin on Wed Apr 02 06:52:01 GMT 2025
|
PRIMARY | |||
|
60714
Created by
admin on Wed Apr 02 06:52:01 GMT 2025 , Edited by admin on Wed Apr 02 06:52:01 GMT 2025
|
PRIMARY | |||
|
31643
Created by
admin on Wed Apr 02 06:52:01 GMT 2025 , Edited by admin on Wed Apr 02 06:52:01 GMT 2025
|
PRIMARY | |||
|
DB00597
Created by
admin on Wed Apr 02 06:52:01 GMT 2025 , Edited by admin on Wed Apr 02 06:52:01 GMT 2025
|
PRIMARY | |||
|
CHEMBL1200593
Created by
admin on Wed Apr 02 06:52:01 GMT 2025 , Edited by admin on Wed Apr 02 06:52:01 GMT 2025
|
PRIMARY | |||
|
760055
Created by
admin on Wed Apr 02 06:52:01 GMT 2025 , Edited by admin on Wed Apr 02 06:52:01 GMT 2025
|
PRIMARY | |||
|
25483
Created by
admin on Wed Apr 02 06:52:01 GMT 2025 , Edited by admin on Wed Apr 02 06:52:01 GMT 2025
|
PRIMARY | RxNorm | ||
|
BB-97
Created by
admin on Wed Apr 02 06:52:01 GMT 2025 , Edited by admin on Wed Apr 02 06:52:01 GMT 2025
|
PRIMARY | |||
|
100000084509
Created by
admin on Wed Apr 02 06:52:01 GMT 2025 , Edited by admin on Wed Apr 02 06:52:01 GMT 2025
|
PRIMARY | |||
|
SUB07866MIG
Created by
admin on Wed Apr 02 06:52:01 GMT 2025 , Edited by admin on Wed Apr 02 06:52:01 GMT 2025
|
PRIMARY | |||
|
m5628
Created by
admin on Wed Apr 02 06:52:01 GMT 2025 , Edited by admin on Wed Apr 02 06:52:01 GMT 2025
|
PRIMARY | Merck Index | ||
|
Gadoteridol
Created by
admin on Wed Apr 02 06:52:01 GMT 2025 , Edited by admin on Wed Apr 02 06:52:01 GMT 2025
|
PRIMARY | |||
|
7549
Created by
admin on Wed Apr 02 06:52:01 GMT 2025 , Edited by admin on Wed Apr 02 06:52:01 GMT 2025
|
PRIMARY | |||
|
DTXSID2048662
Created by
admin on Wed Apr 02 06:52:01 GMT 2025 , Edited by admin on Wed Apr 02 06:52:01 GMT 2025
|
PRIMARY | |||
|
1287631
Created by
admin on Wed Apr 02 06:52:01 GMT 2025 , Edited by admin on Wed Apr 02 06:52:01 GMT 2025
|
PRIMARY | |||
|
0199MV609F
Created by
admin on Wed Apr 02 06:52:01 GMT 2025 , Edited by admin on Wed Apr 02 06:52:01 GMT 2025
|
PRIMARY | |||
|
0199MV609F
Created by
admin on Wed Apr 02 06:52:01 GMT 2025 , Edited by admin on Wed Apr 02 06:52:01 GMT 2025
|
PRIMARY | |||
|
C65796
Created by
admin on Wed Apr 02 06:52:01 GMT 2025 , Edited by admin on Wed Apr 02 06:52:01 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
IMPURITY -> PARENT |
|
||
|
|
IMPURITY -> PARENT | |||
|
|
IMPURITY -> PARENT |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |