SCHEMBL4304653

SCHEMBL4304653

c1ccc(CN2CC3CCCN[C@@H]3C2)cc1

nearest known ligand 0.54

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
▸ FUCA1 P04066 2/20 0.45
▸ CYP1A2 P05177 1/20 0.44
▸ CYP3A4 P08684 1/20 0.44
▸ CYP2D6 P10635 1/20 0.44
▸ CYP2C19 P33261 1/20 0.44
▸ ALDH1A1 P00352 1/20 0.44
▸ SIGMAR1 Q99720 2/20 0.44
▸ DRD2 P14416 2/20 0.43
▸ DRD3 P35462 2/20 0.43
▸ ACHE P22303 2/20 0.42
▸ BCHE P06276 1/20 0.42
▸ BACE1 P56817 1/20 0.42
▸ OPRL1 P41146 1/20 0.42

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
SCHEMBL697958 1.00 FUCA1 (0.45) FUCA1CYP1A2CYP3A4CYP2D6CYP2C19
SCHEMBL13992425 1.00 FUCA1 (0.45) FUCA1CYP1A2CYP3A4CYP2D6CYP2C19
SCHEMBL4303371 1.00 FUCA1 (0.45) FUCA1CYP1A2CYP3A4CYP2D6CYP2C19
SCHEMBL1724302 1.00 FUCA1 (0.45) FUCA1CYP1A2CYP3A4CYP2D6CYP2C19
SCHEMBL1983745 1.00 FUCA1 (0.45) FUCA1CYP1A2CYP3A4CYP2D6CYP2C19
Hydrochloric Acid SCHEMBL2339005 0.98 FUCA1 (0.44) FUCA1CYP1A2CYP3A4CYP2D6CYP2C19
Hydrochloric Acid SCHEMBL2348540 0.98 FUCA1 (0.44) FUCA1CYP1A2CYP3A4CYP2D6CYP2C19
Hydrochloric Acid SCHEMBL2542931 0.98 FUCA1 (0.44) FUCA1CYP1A2CYP3A4CYP2D6CYP2C19
SCHEMBL17228289 0.95 POLB (0.46) FUCA1CYP1A2CYP3A4CYP2D6CYP2C19
Isopropyl Alcohol SCHEMBL29020804 0.92 GRIN2B (0.44) FUCA1ALDH1A1ACHEBCHE

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 12 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2009125425-A2 IMPROVED PROCESS FOR THE PREPARATION OF (S.S)-2.8-DIAZABICYCLO[4.3.0]NONANE NEULAND LABORATORIES LTD (IN) 2009-10-15 — — WO claimed
EP-1077979-B1 METHOD FOR PRODUCING (S,S)-BENZYL-2,8-DIAZABICYCLO 4.3.0]NONANE BAYER HEALTHCARE AG (DE) 2005-07-06 — — EP claimed
US-6235908-B1 PREPARATION OF TARTRATE BAYER AKTIENGESELLSCHAFT (DE) 2001-05-22 — — US claimed
US-8680276-B2 Synthesis of (4aS,7aS)-octahydro-1H-pyrrolo[3,4-b]pyridine F.I.S. FABBRICA ITALIANA SINTETICI S.P.A (IT) 2014-03-25 — — US disclosed
US-8680276-B2 Synthesis of (4aS,7aS)-octahydro-1H-pyrrolo[3,4-b]pyridine F.I.S. FABBRICA ITALIANA SINTETICI S.P.A (IT) 2014-03-25 — — US disclosed
WO-2010100215-A1 SYNTHESIS OF (4aS,7aS)-OCTAHYDRO-1H-PYRROLO[3,4-b]PYRIDINE F.I.S. FABBRICA ITALIANA SINTETICI S.P.A. (IT) 2010-09-10 — — WO disclosed
WO-2009125425-A2 IMPROVED PROCESS FOR THE PREPARATION OF (S.S)-2.8-DIAZABICYCLO[4.3.0]NONANE NEULAND LABORATORIES LTD (IN) 2009-10-15 — — WO disclosed
EP-1077979-B1 METHOD FOR PRODUCING (S,S)-BENZYL-2,8-DIAZABICYCLO 4.3.0]NONANE BAYER HEALTHCARE AG (DE) 2005-07-06 — — EP disclosed
US-6235908-B1 PREPARATION OF TARTRATE BAYER AKTIENGESELLSCHAFT (DE) 2001-05-22 — — US disclosed
US-6235908-B1 PREPARATION OF TARTRATE BAYER AKTIENGESELLSCHAFT (DE) 2001-05-22 — — US disclosed
EP-1077979-A1 METHOD FOR PRODUCING (S,S)-BENZYL-2,8-DIAZABICYCLO 4.3.0]NONANE BAYER AG (DE) 2001-02-28 — — EP disclosed
WO-1999058532-A1 METHOD FOR PRODUCING (S,S)-BENZYL-2,8-DIAZABICYCLO[4.3.0]NONANE BAYER AKTIENGESELLSCHAFT (DE) 1999-11-18 — — WO disclosed
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