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Details

Stereochemistry ABSOLUTE
Molecular Formula C34H31F3N2O2
Molecular Weight 556.6173
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of WAY-204688

SMILES

COC1=C(C=CC=C1)[C@H](C2=CC=CC3=C2C=CC=C3)[C@@](C)(C#N)C(=O)N4CCC(CC4)C5=CC(=CC=C5)C(F)(F)F

InChI

InChIKey=JZPONCMNBSEYQW-CQTOTRCISA-N
InChI=1S/C34H31F3N2O2/c1-33(22-38,32(40)39-19-17-23(18-20-39)25-11-7-12-26(21-25)34(35,36)37)31(29-14-5-6-16-30(29)41-2)28-15-8-10-24-9-3-4-13-27(24)28/h3-16,21,23,31H,17-20H2,1-2H3/t31-,33+/m0/s1

HIDE SMILES / InChI

Description
Curator's Comment: Description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/16317384 | https://www.ncbi.nlm.nih.gov/pubmed/17902637

Juvantia Pharma and Orion developed ORM-12741, also known as ORM-10921, a novel selective antagonist of alpha-2C adrenoceptors for the treatment of depression and Alzheimer's disease. ORM-12741 participated in phase II clinical trial where was evaluated the safety and efficacy of the drug in patients with Alzheimer's disease. In spite of the successfully completed phase II, further study of the drug for this disease was discontinued. In addition, ORM-12741 participated in clinical trial phase II to prove the concept that this drug could prevent blood vessel spasms for Raynaud's phenomenon. Raynaud's phenomenon is a disorder of the digital blood vessels resulting in episodic impairment of blood flow. However, this study was terminated because of the recommendation by study Data and Safety Monitoring Committee to the sponsor following the interim analysis of 8 subjects.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
The α2C-adrenoceptor antagonist, ORM-10921, exerts antidepressant-like effects in the Flinders Sensitive Line rat.
2017-02
Tolerability of ORM-12741 and effects on episodic memory in patients with Alzheimer's disease.
2017-01
Therapeutic Potential of Selectively Targeting the α2C-Adrenoceptor in Cognition, Depression, and Schizophrenia-New Developments and Future Perspective.
2017
The α2C-adrenoceptor antagonist, ORM-10921, has antipsychotic-like effects in social isolation reared rats and bolsters the response to haloperidol.
2016-11-03
A double-blind, randomized, placebo-controlled crossover trial of the α2C-adrenoceptor antagonist ORM-12741 for prevention of cold-induced vasospasm in patients with systemic sclerosis.
2014-05
Estrogen receptor dependent inhibitors of NF-kappaB transcriptional activation-1 synthesis and biological evaluation of substituted 2-cyanopropanoic acid derivatives: pathway selective inhibitors of NF-kappaB, a potential treatment for rheumatoid arthritis.
2007-11-01
The activity of pathway-selective estrogen receptor ligands in experimental septic shock.
2005-12
Patents

Patents

Sample Use Guides

Name Type Language
SIM688
Preferred Name English
WAY-204688
Code English
WAY204688
Code English
(2R)-2-((S)-(2-METHOXYPHENYL)-(1-NAPHTHYL)METHYL)-2-METHYL-3-OXO-3-(4-(3-(TRIFLUOROMETHYL)PHENYL)-1-PIPERIDYL)PROPANENITRILE
Systematic Name English
PIPERIDINE, 1-((2S,3S)-2-CYANO-3-(2-METHOXYPHENYL)-2-METHYL-3-(1-NAPHTHALENYL)-1-OXOPROPYL)-4-(3-(TRIFLUOROMETHYL)PHENYL)-
Systematic Name English
Code System Code Type Description
PUBCHEM
9829162
Created by admin on Mon Mar 31 18:02:20 GMT 2025 , Edited by admin on Mon Mar 31 18:02:20 GMT 2025
PRIMARY
WIKIPEDIA
WAY-204688
Created by admin on Mon Mar 31 18:02:20 GMT 2025 , Edited by admin on Mon Mar 31 18:02:20 GMT 2025
PRIMARY
FDA UNII
QT9VF4MW6U
Created by admin on Mon Mar 31 18:02:20 GMT 2025 , Edited by admin on Mon Mar 31 18:02:20 GMT 2025
PRIMARY
EPA CompTox
DTXSID701336370
Created by admin on Mon Mar 31 18:02:20 GMT 2025 , Edited by admin on Mon Mar 31 18:02:20 GMT 2025
PRIMARY
CAS
796854-35-8
Created by admin on Mon Mar 31 18:02:20 GMT 2025 , Edited by admin on Mon Mar 31 18:02:20 GMT 2025
PRIMARY
MANUFACTURER PRODUCT INFORMATION
SIM-688
Created by admin on Mon Mar 31 18:02:20 GMT 2025 , Edited by admin on Mon Mar 31 18:02:20 GMT 2025
PRIMARY HY-19498 CAS:796854-35-8 (Synonyms WAY 204688, WAY204688, SIM 688, SIM688, SIM-688)