SCHEMBL3316692

SCHEMBL3316692

N[C@H]1CCc2c(F)cc(F)cc2C1

nearest known ligand 0.59

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
DRD2 P14416 5/20 0.59
DRD3 P35462 5/20 0.59
MAPT P10636 2/20 0.43
NFKB1 P19838 1/20 0.43
THPO P40225 1/20 0.43
HIF1A Q16665 1/20 0.43
HSD17B10 Q99714 1/20 0.43
USP2 O75604 1/20 0.43
ALDH1A1 P00352 1/20 0.43
KDM4E B2RXH2 1/20 0.42
PLAU P00749 1/20 0.41
OPRK1 P41145 1/20 0.40
ADRA1A P35348 1/20 0.36

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
SCHEMBL6958473 1.00 DRD2 (0.59) DRD2DRD3MAPTNFKB1THPO
SCHEMBL30057164 1.00 DRD2 (0.59) DRD2DRD3MAPTNFKB1THPO
SCHEMBL30059639 1.00 DRD2 (0.59) DRD2DRD3MAPTNFKB1THPO
SCHEMBL754233 1.00 DRD2 (0.59) DRD2DRD3MAPTNFKB1THPO
SCHEMBL30058138 1.00 DRD2 (0.59) DRD2DRD3MAPTNFKB1THPO
Hydrochloric Acid SCHEMBL754377 0.98 DRD2 (0.57) DRD2DRD3MAPTNFKB1THPO
Bromide SCHEMBL30426257 0.98 DRD2 (0.57) DRD2DRD3MAPTNFKB1THPO
Hydrochloric Acid SCHEMBL754376 0.98 DRD2 (0.57) DRD2DRD3MAPTNFKB1THPO
Bromide SCHEMBL29016368 0.98 DRD2 (0.57) DRD2DRD3MAPTNFKB1THPO
Hydrochloric Acid SCHEMBL30059645 0.98 DRD2 (0.57) DRD2DRD3MAPTNFKB1THPO

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117867045-A Method for synthesizing (S) -5, 7-difluoro-1, 2,3, 4-tetrahydronaphthalene-2-amine by biological enzyme method 中国科学院青岛生物能源与过程研究所 2024-04-12 CN claimed
US-20100105748-A1 METHODS AND COMPOSITIONS FOR TREATMENT OF DRUG ADDICTION NATIONAL INSTITUTES OF HEALTH-DIRECTOR DEITR 2010-04-29 US claimed
WO-2008115706-A1 METHODS AND COMPOSITIONS FOR TREATMENT OF DRUG ADDICTION EMORY UNIVERSITY (US) 2008-09-25 WO claimed
EP-0757677-B1 BENZOCYCLOHEXYLIMIDAZOLETHIONE DERIVATIVES SYNTEX LLC (US) 2003-06-18 EP claimed
US-5719280-A REACTING AMINE SUBSTITUTED BENZOCYCLOALKANE WITH DIALKYLOXYACETALDEHYDE IN PRESENCE OF REDUCING AGENT OR CATALYTIC HYDROGENATION, TREATING WITH THIOCYANIC ACID SYNTEX (U.S.A.) INC. (US) 1998-02-17 US claimed
EP-0757677-A1 BENZOCYCLOALKYLAZOLETHIONE DERIVATIVES SYNTEX (U.S.A.) INC. (US) 1997-02-12 EP claimed
WO-1995029165-A2 BENZOCYCLOALKYLAZ0LETHIONE DERIVATIVES AS DOPAMIN BETA-HYDROXYLASE INHIBITORS SYNTEX (U.S.A.) INC. (US) 1995-11-02 WO claimed
CN-117867045-A Method for synthesizing (S) -5, 7-difluoro-1, 2,3, 4-tetrahydronaphthalene-2-amine by biological enzyme method 中国科学院青岛生物能源与过程研究所 2024-04-12 CN disclosed
CN-117867045-A Method for synthesizing (S) -5, 7-difluoro-1, 2,3, 4-tetrahydronaphthalene-2-amine by biological enzyme method 中国科学院青岛生物能源与过程研究所 2024-04-12 CN disclosed
CN-117867045-A Method for synthesizing (S) -5, 7-difluoro-1, 2,3, 4-tetrahydronaphthalene-2-amine by biological enzyme method 中国科学院青岛生物能源与过程研究所 2024-04-12 CN disclosed
CN-113527108-B Process for preparing optically pure 5, 7-difluoro-1, 2,3, 4-tetrahydronaphthalen-2-amine and salts thereof 斯芬克司药物研发(天津)股份有限公司 2022-10-25 CN disclosed
CN-113527108-A Process for preparing optically pure 5, 7-difluoro-1, 2,3, 4-tetrahydronaphthalen-2-amine and salts thereof 斯芬克司药物研发(天津)股份有限公司 2021-10-22 CN disclosed
US-20130274303-A1 METHODS AND COMPOSITIONS FOR TREATMENT OF DRUG ADDICTION YALE UNIVERSITY (US) 2013-10-17 US disclosed
US-20100105748-A1 METHODS AND COMPOSITIONS FOR TREATMENT OF DRUG ADDICTION NATIONAL INSTITUTES OF HEALTH-DIRECTOR DEITR 2010-04-29 US disclosed
WO-2008115706-A1 METHODS AND COMPOSITIONS FOR TREATMENT OF DRUG ADDICTION EMORY UNIVERSITY (US) 2008-09-25 WO disclosed
EP-0757677-B1 BENZOCYCLOHEXYLIMIDAZOLETHIONE DERIVATIVES SYNTEX LLC (US) 2003-06-18 EP disclosed
US-5719280-A REACTING AMINE SUBSTITUTED BENZOCYCLOALKANE WITH DIALKYLOXYACETALDEHYDE IN PRESENCE OF REDUCING AGENT OR CATALYTIC HYDROGENATION, TREATING WITH THIOCYANIC ACID SYNTEX (U.S.A.) INC. (US) 1998-02-17 US disclosed
EP-0757677-A1 BENZOCYCLOALKYLAZOLETHIONE DERIVATIVES SYNTEX (U.S.A.) INC. (US) 1997-02-12 EP disclosed
US-5538988-A CARDIOVASCULAR DISORDERS AND DOPAMINE HYDROLASE ENZYME INHIBITORS SYNTEX (U.S.A.) INC. 1996-07-23 US disclosed
WO-1995029165-A2 BENZOCYCLOALKYLAZ0LETHIONE DERIVATIVES AS DOPAMIN BETA-HYDROXYLASE INHIBITORS SYNTEX (U.S.A.) INC. (US) 1995-11-02 WO disclosed