SCHEMBL7440864

SCHEMBL7440864

Nn1ccc2c3c(ccc21)CCCC3

nearest known ligand 0.35

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
NOS3 P29474 1/20 0.35
NOS1 P29475 1/20 0.35
NOS2 P35228 1/20 0.35
CA1 P00915 3/20 0.33
CA2 P00918 3/20 0.33
BCL2L1 Q07817 1/20 0.33
BAD Q92934 1/20 0.33
KIF11 P52732 1/20 0.33
HTR6 P50406 1/20 0.33
CES1 P23141 1/20 0.31
GRIA1 P42261 1/20 0.30
GRIA2 P42262 1/20 0.30
GRIA3 P42263 1/20 0.30
GRIA4 P48058 1/20 0.30

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
SCHEMBL1278375 0.67 BCL2L1 (0.52) NOS3NOS1NOS2BCL2L1BAD
SCHEMBL25520831 0.66 HTR2C (0.37) HTR6
SCHEMBL25520840 0.66 NR3C1 (0.32) HTR6
SCHEMBL9461283 0.65 BCL2L1 (0.50) NOS3NOS1NOS2BCL2L1BAD
SCHEMBL6835829 0.63 NOS3 (0.47) NOS3NOS1NOS2BCL2L1BAD
SCHEMBL8402725 0.63 NOS3 (0.47) NOS3NOS1NOS2BCL2L1BAD
SCHEMBL12367273 0.63 ALOX5 (0.38) NOS3NOS1NOS2BCL2L1BAD
SCHEMBL23944932 0.62 PARP1 (0.46) NOS3NOS1NOS2CA1CA2
SCHEMBL20112700 0.60 CES1 (0.52) NOS3NOS1NOS2BCL2L1BAD
SCHEMBL14354818 0.60 BCL2L1 (0.47) NOS3NOS1NOS2BCL2L1BAD

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
JP-57126472-A None JP disclosed
EP-0690843-B1 Formyl- or cyano- substituted indole derivatives having dopaminergic activity UPJOHN CO (US) 2000-08-30 EP disclosed
US-5639778-A TREATING CENTRAL NERVOUS SYSTEM DISORDERS PHARMACIA & UPJOHN COMPANY (US) 1997-06-17 US disclosed
EP-0690843-A1 INDOLETETRALINS HAVING DOPAMINERGIC ACTIVITY PHARMACIA & UPJOHN COMPANY (US) 1996-01-10 EP disclosed
WO-1994021608-A1 INDOLETETRALINS HAVING DOPAMINERGIC ACTIVITY THE UPJOHN COMPANY (US) 1994-09-29 WO disclosed
US-5302599-A Administering for central nervous system and cardiovascular disorders THE UPJOHN COMPANY (US) 1994-04-12 US disclosed
EP-0055043-B1 6,7,8,9-TETRAHYDRO-3H-BENZ(E)INDOLAMINE DERIVATIVES, PROCESSES FOR THEIR PREPARATION AND INTERMEDIATES USED THEREIN, AND PHARMACEUTICAL COMPOSITIONS CONTAINING THE INDOLAMINE DERIVATIVES AYERST, MCKENNA AND HARRISON INC. (CA) 1985-01-23 EP disclosed
EP-0055043-B1 6,7,8,9-TETRAHYDRO-3H-BENZ(E)INDOLAMINE DERIVATIVES, PROCESSES FOR THEIR PREPARATION AND INTERMEDIATES USED THEREIN, AND PHARMACEUTICAL COMPOSITIONS CONTAINING THE INDOLAMINE DERIVATIVES AYERST, MCKENNA AND HARRISON INC. (CA) 1985-01-23 EP disclosed
EP-0055043-A3 6,7,8,9-TETRAHYDRO-3H-BENZ(E)INDOLAMINE DERIVATIVES, PROCESSES FOR THEIR PREPARATION AND INTERMEDIATES USED THEREIN, AND PHARMACEUTICAL COMPOSITIONS CONTAINING THE INDOLAMINE DERIVATIVES 1982-09-08 EP disclosed
JP-S57126472-A 6,7,8,9-TETRAHYDRO-3H-BENZ(E)INDOLEAMINE DERIVATIVE AYERST MCKENNA & HARRISON 1982-08-06 JP disclosed
EP-0055043-A2 6,7,8,9-Tetrahydro-3H-benz(e)indolamine derivatives, processes for their preparation and intermediates used therein, and pharmaceutical compositions containing the indolamine derivatives AYERST, MCKENNA AND HARRISON INC. (CA) 1982-06-30 EP disclosed
EP-0055043-A2 6,7,8,9-Tetrahydro-3H-benz(e)indolamine derivatives, processes for their preparation and intermediates used therein, and pharmaceutical compositions containing the indolamine derivatives AYERST, MCKENNA AND HARRISON INC. (CA) 1982-06-30 EP disclosed