SCHEMBL8580359

SCHEMBL8580359

N#CC1(c2ccccc2)CCN([O-])CC1.[Na+]

nearest known ligand 0.67

Known targets — ChEMBL curated mechanism

ABCC8ACEADORA1ADORA2AADORA2BADORA3ALDH5A1ALOX5ALOX5APATP4AATP4BBRAFCA1CA12CA2CA4CYSLTR1DHFRDPEP1EDNRAEDNRBESR2F10FDPSFGF1GABBR1GABBR2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGARTGNRHRGSC1HMGCRIMPDH1IMPDH2KCNJ11LY96NOD2NR3C1NS3NS4ANS5bP2RY1P2RY12P2RY2P2RY4P2RY6PBP2XPDE3APDE3BPDE4APDE4BPDE4CPDE4DPDK1PDK2PDK3PDK4PPARGPPATPTGIRPTGS1PTGS2RAF1RYR1RYR3SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASERPINC1SLC12A1SLC12A3SYKTHRATHRBTLR3TLR4TLR9TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYMSVKORC1XDHblablaIMP-1blaOXA-33blaOXA-58blaT-3blaT-4blaT-5blaT-6dacAdacBdacCfolAfolPfolP1ftsIfusAgaggyrAgyrBmecAmrcAmrcBmrdApbp1apbp1bpbp2pbp2apbp2bpbp3pbp4pbpApbpBpbpCpbpFpolponBrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpoArpoBrpoCrpoZrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

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 11)

geneUniProtsupporting neighboursconfidence
CA12 known ✓ O43570 2/20 0.60
CA1 known ✓ P00915 2/20 0.60
CA2 known ✓ P00918 2/20 0.60
CA9 Q16790 2/20 0.60
OPRM1 P35372 2/20 0.59
OPRD1 P41143 1/20 0.54
OPRL1 P41146 3/20 0.50
CA7 P43166 1/20 0.49
CA14 Q9ULX7 1/20 0.49
MEN1 O00255 1/20 0.47
KMT2A Q03164 1/20 0.47

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
SCHEMBL432561 0.80 OPRM1 (0.59) CA12CA1CA2CA9OPRM1
SCHEMBL504355 0.80 OPRM1 (0.70) CA12CA1CA2CA9OPRM1
SCHEMBL21077925 0.80 OPRM1 (0.61) CA12CA1CA2CA9OPRM1
SCHEMBL13548727 0.80 OPRM1 (0.66) CA12CA1CA2CA9OPRM1
SCHEMBL11211164 0.80 OPRM1 (0.61) CA12CA1CA2CA9OPRM1
SCHEMBL3604273 0.79 OPRM1 (0.59) CA12CA1CA2CA9OPRM1
Hydrochloric Acid SCHEMBL3595890 0.79 OPRM1 (0.73) OPRM1OPRD1KMT2A
SCHEMBL15963271 0.79 OPRM1 (0.59) CA12CA1CA2CA9OPRM1
SCHEMBL13801253 0.77 OPRM1 (0.58) CA12CA1CA2CA9OPRM1
SCHEMBL26136926 0.77 OPRM1 (0.58) CA12CA1CA2CA9OPRM1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5756748-A ALKYLATING 4-CYANO-4-PHENYLPIPERIDINE, PRECIPITATING AS HYDROCHLORIDE SALT, HYDROLYZING TO ACID, REACTING WITH OXALYL CHLORIDE OR THIONYL CHLORIDE AND ETHYLMETHYLAMINE TO FORM AMIDE ASTRA AB (SE) 1998-05-26 US disclosed