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Details

Stereochemistry ABSOLUTE
Molecular Formula C32H29NO5
Molecular Weight 507.5764
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of OLODANRIGAN

SMILES

COC1=CC=C2CN([C@@H](CC2=C1OCC3=CC=CC=C3)C(O)=O)C(=O)C(C4=CC=CC=C4)C5=CC=CC=C5

InChI

InChIKey=GHBCIXGRCZIPNQ-MHZLTWQESA-N
InChI=1S/C32H29NO5/c1-37-28-18-17-25-20-33(31(34)29(23-13-7-3-8-14-23)24-15-9-4-10-16-24)27(32(35)36)19-26(25)30(28)38-21-22-11-5-2-6-12-22/h2-18,27,29H,19-21H2,1H3,(H,35,36)/t27-/m0/s1

HIDE SMILES / InChI

Molecular Formula C32H29NO5
Molecular Weight 507.5764
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Olodanrigan (EMA-401) is an angiotensin II type 2 receptor antagonist. Olodanrigan may act on paracrine/autocrine mechanisms at peripheral nerve terminals, or intracrine mechanisms, to reduce neuropathic pain signalling in AngII/NGF/TRPV1-convergent pathways. Olodanrigan is being developed by Novartis for the treatment of neuropathic pain.

Approval Year

Targets

Targets

PubMed

PubMed

TitleDatePubMed
EMA401, an orally administered highly selective angiotensin II type 2 receptor antagonist, as a novel treatment for postherpetic neuralgia: a randomised, double-blind, placebo-controlled phase 2 clinical trial.
2014 May 10
Development of EMA401 as an orally-administered, highly-selective angiotensin II type 2 receptor antagonist for the treatment of neuropathic pain.
2014 Oct
Mechanisms underlying clinical efficacy of Angiotensin II type 2 receptor (AT2R) antagonist EMA401 in neuropathic pain: clinical tissue and in vitro studies.
2015 Jun 26
EMA401: an old antagonist of the AT2R for a new indication in neuropathic pain.
2017

Sample Use Guides

A pilot phase IIa study demonstrated the efficacy and safety of the drug taken twice daily as two capsules of 50 mg (400 mg/day).
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Sat Dec 16 07:59:08 UTC 2023
Edited
by admin
on Sat Dec 16 07:59:08 UTC 2023
Record UNII
P0FN522VTO
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
OLODANRIGAN
INN  
Official Name English
olodanrigan [INN]
Common Name English
EMA401
Code English
Olodanrigan [WHO-DD]
Common Name English
EMA-401
Code English
3-ISOQUINOLINECARBOXYLIC ACID, 2-(2,2-DIPHENYLACETYL)-1,2,3,4-TETRAHYDRO-6-METHOXY-5-(PHENYLMETHOXY)-, (3S)-
Systematic Name English
PD-126055
Code English
Code System Code Type Description
CAS
1316755-16-4
Created by admin on Sat Dec 16 07:59:08 UTC 2023 , Edited by admin on Sat Dec 16 07:59:08 UTC 2023
PRIMARY
FDA UNII
P0FN522VTO
Created by admin on Sat Dec 16 07:59:08 UTC 2023 , Edited by admin on Sat Dec 16 07:59:08 UTC 2023
PRIMARY
NCI_THESAURUS
C174823
Created by admin on Sat Dec 16 07:59:08 UTC 2023 , Edited by admin on Sat Dec 16 07:59:08 UTC 2023
PRIMARY
SMS_ID
100000177040
Created by admin on Sat Dec 16 07:59:08 UTC 2023 , Edited by admin on Sat Dec 16 07:59:08 UTC 2023
PRIMARY
PUBCHEM
9937291
Created by admin on Sat Dec 16 07:59:08 UTC 2023 , Edited by admin on Sat Dec 16 07:59:08 UTC 2023
PRIMARY
EPA CompTox
DTXSID101031601
Created by admin on Sat Dec 16 07:59:08 UTC 2023 , Edited by admin on Sat Dec 16 07:59:08 UTC 2023
PRIMARY
INN
10476
Created by admin on Sat Dec 16 07:59:08 UTC 2023 , Edited by admin on Sat Dec 16 07:59:08 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY