SCHEMBL7867337

SCHEMBL7867337

CCc1ccc2c(C3CCNCC3)c[nH]c2c1.Cc1ccc(S(=O)(=O)O)cc1

nearest known ligand 0.43

Known targets — ChEMBL curated mechanism

ABL1BMXBRAFBTKCHRNA4CHRNB2CSNK1EEGFRERBB2F10FLT1FLT3FLT4IGF1RINSRITKJAK3KDRKITOPRM1PARP1PARP2PDGFRBPIK3CDRAF1RETSLC18A2TECTXKdacAdacBdacCftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of None. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
APP P05067 5/20 0.43
HTR6 P50406 3/20 0.43
HTR2C P28335 2/20 0.43
ADRB2 P07550 1/20 0.43
NMT2 O60551 1/20 0.40
NMT1 P30419 1/20 0.40
DRD2 P14416 2/20 0.39
SLC6A4 P31645 1/20 0.39
HTR2A P28223 1/20 0.38
HTR7 P34969 1/20 0.38
KCNH2 Q12809 1/20 0.38
GABRP O00591 1/20 0.38
GABRD O14764 1/20 0.38
GABRA1 P14867 1/20 0.38
GABRB1 P18505 1/20 0.38
GABRG2 P18507 1/20 0.38
GABRB3 P28472 1/20 0.38
GABRA5 P31644 1/20 0.38
GABRA3 P34903 1/20 0.38
GABRA2 P47869 1/20 0.38

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
Bromide SCHEMBL8820726 0.85 APP (0.41) APPHTR6HTR2CADRB2DRD2
SCHEMBL7867549 0.81 HTR6 (0.42) HTR6DRD2SLC6A4GABRA1GABRB2
SCHEMBL7867983 0.81 HTR1D (0.41) HTR6NMT2NMT1SLC6A4GABRA1
SCHEMBL7870932 0.79 HTR6 (0.42) HTR6DRD2SLC6A4CYP2D6
SCHEMBL7870768 0.78 HTR6 (0.39) HTR6HTR7CYP2D6
SCHEMBL7859777 0.78 HTR6 (0.44) HTR6HTR2CADRB2HTR1FCCR2
SCHEMBL7859788 0.76 MAPT (0.41) HTR6CYP2D6
SCHEMBL4676883 0.76 HTR2C (0.62) APPHTR2CADRB2DRD2SLC6A4
SCHEMBL7870665 0.75 MAPT (0.46) HTR6HTR2CDRD2HTR1DCYP2D6
SCHEMBL9006995 0.75 SLC6A4 (0.49) APPHTR2CADRB2DRD2SLC6A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1077213-A2 Inhibition of serotonin reuptake ELI LILLY AND COMPANY (US) 2001-02-21 EP disclosed
US-6046215-A A PIPERIDINYLBENZOTHIOPHENES USEFUL FOR TRATING BRAIN DISORDERS ELI LILLY AND COMPANY (US) 2000-04-04 US disclosed
US-5846982-A Inhibition of serotonin reuptake ELI LILLY AND COMPANY (US) 1998-12-08 US disclosed
EP-0812826-A1 1H-indole and benzo(b)thiophene derivatives with 4-(1,2,3,6-tetra:hydro:pyridinyl)- and 4-piperidinyl-groups bound to the heterocyclic ring as inhibitors of serotonin reuptake ELI LILLY AND COMPANY (US) 1997-12-17 EP disclosed