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Details

Stereochemistry ABSOLUTE
Molecular Formula C32H28NO5.Na
Molecular Weight 529.5582
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of OLODANRIGAN SODIUM

SMILES

[Na+].COC1=C(OCC2=CC=CC=C2)C3=C(CN([C@@H](C3)C([O-])=O)C(=O)C(C4=CC=CC=C4)C5=CC=CC=C5)C=C1

InChI

InChIKey=AKMGNOBRQGBYJM-YCBFMBTMSA-M
InChI=1S/C32H29NO5.Na/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);/q;+1/p-1/t27-;/m0./s1

HIDE SMILES / InChI

Molecular Formula Na
Molecular Weight 22.98976928
Charge 1
Count
MOL RATIO 1 MOL RATIO (average)
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C32H28NO5
Molecular Weight 506.5684
Charge -1
Count
MOL RATIO 1 MOL RATIO (average)
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Description

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.

Originator

Approval Year

Targets

Primary TargetPharmacologyConditionPotency
0.6 nM [IC50]

PubMed

Sample Use Guides

In Vivo Use Guide
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
Record UNII
P9EW7EP34P
Record Status Validated (UNII)
Record Version