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Details

Stereochemistry ACHIRAL
Molecular Formula C27H30N2O2
Molecular Weight 414.5393
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of Palovarotene

SMILES

CC1(C)CCC(C)(C)C2=C1C=C(CN3C=CC=N3)C(\C=C\C4=CC=C(C=C4)C(O)=O)=C2

InChI

InChIKey=YTFHCXIPDIHOIA-DHZHZOJOSA-N
InChI=1S/C27H30N2O2/c1-26(2)12-13-27(3,4)24-17-22(18-29-15-5-14-28-29)21(16-23(24)26)11-8-19-6-9-20(10-7-19)25(30)31/h5-11,14-17H,12-13,18H2,1-4H3,(H,30,31)/b11-8+

HIDE SMILES / InChI

Molecular Formula C27H30N2O2
Molecular Weight 414.5393
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Palovarotene (R-667, RO-3300074) was developed by Roche Holding AG as a selective retinoic acid receptor gamma agonist for the treatment of emphysema. Phase I clinical trials of palovarotene in patients with emphysema demonstrated that the drug is well tolerated, with improvements observed in markers of emphysema progression. Unlike all-trans retinoic acid, the pharmacokinetic profile of palovarotene appears to be dose-proportional. However, those studies were discontinued. Palovarotene is also being investigated in phase II of the clinical trial in the treatment of Fibrodysplasia Ossificans Progressiva (FOP). Palovarotene received Fast Track designation from the U.S. Food and Drug Administration (FDA) and orphan designations for the treatment of FOP from both the FDA and the European Medicines Agency (EMA).

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
10.3 ng/mL
1 mg 1 times / day multiple, oral
dose: 1 mg
route of administration: Oral
experiment type: MULTIPLE
co-administered:
PALOVAROTENE plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FED
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
57.7 ng × h/mL
1 mg 1 times / day multiple, oral
dose: 1 mg
route of administration: Oral
experiment type: MULTIPLE
co-administered:
PALOVAROTENE plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FED
Sourcing

Sourcing

Vendor/AggregatorIDURL
PubMed

PubMed

TitleDatePubMed
Treatment of patients who have fibrodysplasia ossificans progressiva with isotretinoin.
1998 Jan
Palovarotene, a novel retinoic acid receptor gamma agonist for the treatment of emphysema.
2009 Nov
Retinoid treatment of Emphysema in Patients on the Alpha-1 International Registry. The REPAIR study: study design, methodology and quality control of study assessments.
2010 Dec
Potent inhibition of heterotopic ossification by nuclear retinoic acid receptor-γ agonists.
2011 Apr
Patents

Patents

Sample Use Guides

double-blind, placebo-controlled randomised study to assess the safety and efficacy of 5 mg·day(-1) palovarotene given for 1 year to 262 patients with severe α(1)-antitrypsin deficiency and emphysema confirmed by computed tomography.
Route of Administration: Oral
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:36:57 GMT 2023
Edited
by admin
on Fri Dec 15 16:36:57 GMT 2023
Record UNII
28K6I5M16G
Record Status Validated (UNII)
Record Version
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Name Type Language
Palovarotene
INN   USAN   WHO-DD  
INN   USAN  
Official Name English
CLM-001
Code English
RO3300074
Code English
RG-667
Code English
Benzoic acid, 4-[(1E)-2-[5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-3-(1H-pyrazol-1-ylmethyl)-2-naphthalenyl]ethenyl]-
Systematic Name English
4-{(1E)-2-[5,5,8,8-Tetramethyl-3-(1H-pyrazol-1-ylmethyl)-5,6,7,8-tetrahydronaphthalen-2-yl]ethenyl}benzoic acid
Systematic Name English
IPN-60120
Code English
PALOVAROTENE [USAN]
Common Name English
RO-3300074
Code English
palovarotene [INN]
Common Name English
PALOVAROTENE [JAN]
Common Name English
Palovarotene [WHO-DD]
Common Name English
SOHONOS
Brand Name English
IPN60120
Code English
Classification Tree Code System Code
NCI_THESAURUS C804
Created by admin on Fri Dec 15 16:36:58 GMT 2023 , Edited by admin on Fri Dec 15 16:36:58 GMT 2023
FDA ORPHAN DRUG 438714
Created by admin on Fri Dec 15 16:36:58 GMT 2023 , Edited by admin on Fri Dec 15 16:36:58 GMT 2023
FDA ORPHAN DRUG 612117
Created by admin on Fri Dec 15 16:36:58 GMT 2023 , Edited by admin on Fri Dec 15 16:36:58 GMT 2023
EU-Orphan Drug EU/3/14/1368
Created by admin on Fri Dec 15 16:36:58 GMT 2023 , Edited by admin on Fri Dec 15 16:36:58 GMT 2023
Code System Code Type Description
FDA UNII
28K6I5M16G
Created by admin on Fri Dec 15 16:36:58 GMT 2023 , Edited by admin on Fri Dec 15 16:36:58 GMT 2023
PRIMARY
SMS_ID
100000137437
Created by admin on Fri Dec 15 16:36:58 GMT 2023 , Edited by admin on Fri Dec 15 16:36:58 GMT 2023
PRIMARY
EVMPD
SUB75998
Created by admin on Fri Dec 15 16:36:58 GMT 2023 , Edited by admin on Fri Dec 15 16:36:58 GMT 2023
PRIMARY
CAS
410528-02-8
Created by admin on Fri Dec 15 16:36:58 GMT 2023 , Edited by admin on Fri Dec 15 16:36:58 GMT 2023
PRIMARY
EPA CompTox
DTXSID301025696
Created by admin on Fri Dec 15 16:36:58 GMT 2023 , Edited by admin on Fri Dec 15 16:36:58 GMT 2023
PRIMARY
MESH
C546535
Created by admin on Fri Dec 15 16:36:58 GMT 2023 , Edited by admin on Fri Dec 15 16:36:58 GMT 2023
PRIMARY
INN
9025
Created by admin on Fri Dec 15 16:36:58 GMT 2023 , Edited by admin on Fri Dec 15 16:36:58 GMT 2023
PRIMARY
PUBCHEM
10295295
Created by admin on Fri Dec 15 16:36:58 GMT 2023 , Edited by admin on Fri Dec 15 16:36:58 GMT 2023
PRIMARY
USAN
UU-92
Created by admin on Fri Dec 15 16:36:58 GMT 2023 , Edited by admin on Fri Dec 15 16:36:58 GMT 2023
PRIMARY
NCI_THESAURUS
C80661
Created by admin on Fri Dec 15 16:36:58 GMT 2023 , Edited by admin on Fri Dec 15 16:36:58 GMT 2023
PRIMARY
ChEMBL
CHEMBL2105648
Created by admin on Fri Dec 15 16:36:58 GMT 2023 , Edited by admin on Fri Dec 15 16:36:58 GMT 2023
PRIMARY
DRUG BANK
DB12320
Created by admin on Fri Dec 15 16:36:58 GMT 2023 , Edited by admin on Fri Dec 15 16:36:58 GMT 2023
PRIMARY
WIKIPEDIA
Palovarotene
Created by admin on Fri Dec 15 16:36:58 GMT 2023 , Edited by admin on Fri Dec 15 16:36:58 GMT 2023
PRIMARY
Related Record Type Details
TARGET -> AGONIST
Related Record Type Details
ACTIVE MOIETY