Osanetant

Osanetant

SCHEMBL5679271

CC(=O)N(C)C1(c2ccccc2)CCN(CCCC2(c3ccc(Cl)c(Cl)c3)CCCN(C(=O)c3ccccc3)C2)CC1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
TACR2 P21452 17/20 1.00
TACR1 P25103 16/20 1.00
TACR3 P29371 9/20 1.00
CYP3A4 P08684 1/20 1.00
CYP2D6 P10635 1/20 1.00
CYP2C9 P11712 1/20 1.00
CYP2C19 P33261 1/20 1.00
CCR5 P51681 2/20 0.65
HRH1 P35367 1/20 0.49

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Osanetant SCHEMBL119440 1.00 TACR2 (1.00) TACR2TACR1TACR3CYP3A4CYP2D6
Osanetant SCHEMBL30961738 1.00 TACR2 (1.00) TACR2TACR1TACR3CYP3A4CYP2D6
Osanetant SCHEMBL4080131 1.00 TACR2 (1.00) TACR2TACR1TACR3CYP3A4CYP2D6
Osanetant SCHEMBL29371450 1.00 TACR2 (1.00) TACR2TACR1TACR3CYP3A4CYP2D6
Osanetant SCHEMBL5679471 0.99 TACR2 (0.98) TACR2TACR1TACR3CYP3A4CYP2D6
Osanetant SCHEMBL6543149 0.99 TACR2 (0.98) TACR2TACR1TACR3CYP3A4CYP2D6
SCHEMBL8136920 0.97 TACR2 (0.95) TACR2TACR1TACR3CYP3A4CYP2D6
Hydrochloric Acid SCHEMBL6543864 0.97 TACR2 (0.94) TACR2TACR1TACR3CYP3A4CYP2D6
SCHEMBL24855515 0.96 TACR2 (0.92) TACR2TACR1TACR3CYP3A4CYP2D6
SCHEMBL31224281 0.96 TACR2 (0.92) TACR2TACR1TACR3CYP3A4CYP2D6

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 94 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240336565-A1 SOLID FORMS OF OSANETANT ACER THERAPEUTICS INC. 2024-10-10 US claimed
EP-3915560-A1 METHODS OF MANAGING CONDITIONED FEAR WITH NEUROKININ RECEPTOR ANTAGONISTS Emory University (US) 2021-12-01 EP claimed
EP-3160469-B1 METHODS OF MANAGING CONDITIONED FEAR WITH NEUROKININ RECEPTOR ANTAGONISTS UNIV EMORY (US) 2021-04-28 EP claimed
US-10314835-B2 Methods of managing conditioned fear with neurokinin receptor antagonists EMORY UNIVERSITY (US) 2019-06-11 US claimed
US-10052317-B2 Method for treating or preventing hot flushes IMPERIAL INNOVATIONS LIMITED (GB) 2018-08-21 US claimed
US-20170296528-A1 Methods of Managing Conditioned Fear with Neurokinin Receptor Antagonists ACER THERAPEUTICS INC. 2017-10-19 US claimed
EP-3169700-A1 ANTAGONISTS OF NEUROKININ B IN FISH REPRODUCTION Yissum Research Development Company of The Hebrew University of Jerusalem Ltd. (IL) 2017-05-24 EP claimed
EP-3160469-A2 METHODS OF MANAGING CONDITIONED FEAR WITH NEUROKININ RECEPTOR ANTAGONISTS Emory University (US) 2017-05-03 EP claimed
WO-2016009439-A1 ANTAGONISTS OF NEUROKININ B IN FISH REPRODUCTION YISSUME RESEARCH DEVELOMENT COMPANY OF THE HEBREW UNIVERSITY OF JERUSALEM LTD. (IL) 2016-01-21 WO claimed
WO-2015200594-A2 METHODS OF MANAGING CONDITIONED FEAR WITH NEUROKININ RECEPTOR ANTAGONISTS EMORY UNIVERSITY (US) 2015-12-30 WO claimed
EP-0858325-B1 STABLE FREEZE-DRIED PHARMACEUTICAL FORMULATION SANOFI SYNTHELABO (FR) 2002-07-31 EP claimed
US-6294537-B1 NEUROKININS USED FOR TREATMENT OF DISEASES SANOFI-SYNTHELABO (FR) 2001-09-25 US claimed
EP-0673928-B1 Novel N-(3,4-dichlorophenyl-propyl)-piperidine derivatives as selective human NK3-receptor antagonists SANOFI SYNTHELABO (FR) 2001-08-29 EP claimed
US-6124316-A ACTIVE DRUG TREATING PSYCHIATRIC DISEASES, DISEASES OF PSYCHOSOMATIC ORIGIN, OF HYPERTENSION AND, NERVOUS SYSTEM DISORDERS SANOFI (FR) 2000-09-26 US claimed
EP-0673928-A1 Novel N-(3,4-dichlorophenyl-propyl)-piperidine derivatives as selective human NK3-receptor antagonists SANOFI (FR) 1995-09-27 EP claimed
JP-8048669-A None JP disclosed
US-20240336565-A1 SOLID FORMS OF OSANETANT ACER THERAPEUTICS INC. 2024-10-10 US disclosed
WO-1997010211-A1 NOVEL HUMAN NK3 RECEPTOR-SELECTIVE ANTAGONIST COMPOUNDS, METHOD FOR OBTAINING THEM AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM SANOFI (FR) 1997-03-20 WO disclosed
JP-H0848669-A COMPOUND WHICH IS SELECTIVE ANTAGONIST OF HUMAN NK3 RECEPTOR AND USE THEREOF AS MEDICINAL PRODUCT AND DIAGNOSTIC TOOL SANOFI SA 1996-02-20 JP disclosed
EP-0673928-A1 Novel N-(3,4-dichlorophenyl-propyl)-piperidine derivatives as selective human NK3-receptor antagonists SANOFI (FR) 1995-09-27 EP disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (4 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20170296528-A1 Methods of Managing Conditioned Fear with Neurokinin Receptor Antagonists PNMT, TACR2, HTR3C TACR2 2/4885TACR1 6/4885TACR3 31/4885
US-20240336565-A1 SOLID FORMS OF OSANETANT OAT, OPA1, CPS1 TACR2 1620/4885TACR1 898/4885TACR3 2174/4885
US-10052317-B2 Method for treating or preventing hot flushes KLK5, KISS1R, KLKB1 TACR2 10/4885TACR1 11/4885TACR3 7/4885
US-10314835-B2 Methods of managing conditioned fear with neurokinin receptor antagonists PNMT, TACR2, HTR3C TACR2 2/4885TACR1 6/4885TACR3 31/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.