SCHEMBL8867741

SCHEMBL8867741

CC(N)c1ccccc1.Cc1ccc(S(=O)(=O)O)cc1

nearest known ligand 0.62

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
CYP2D6 P10635 2/20 0.62
MAPK1 P28482 1/20 0.62
SMN1; SMN2 Q16637 2/20 0.48
TSHR P16473 2/20 0.48
ALDH1A1 P00352 3/20 0.46
LMNA P02545 2/20 0.45
KDM4E B2RXH2 1/20 0.45
MAPT P10636 1/20 0.45
HTT P42858 1/20 0.45
TDP1 Q9NUW8 1/20 0.45
L3MBTL1 Q9Y468 1/20 0.45
PKM P14618 1/20 0.44
POLB P06746 1/20 0.43
KCNA5 P22460 1/20 0.42
GAA P10253 1/20 0.41
GBA1 P04062 1/20 0.41
BCHE P06276 1/20 0.41
ACHE P22303 1/20 0.41
CA12 O43570 1/20 0.41
CA1 P00915 1/20 0.41

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
SCHEMBL8867724 1.00 CYP2D6 (0.62) CYP2D6MAPK1SMN1; SMN2TSHRALDH1A1
SCHEMBL11236199 0.87 BCHE (0.51) CYP2D6MAPK1SMN1; SMN2TSHRALDH1A1
Isopropylbenzene SCHEMBL4211335 0.86 CYP2D6 (0.61) CYP2D6MAPK1SMN1; SMN2TSHRALDH1A1
SCHEMBL28508065 0.85 CYP2D6 (0.61) CYP2D6MAPK1SMN1; SMN2TSHRALDH1A1
Phenylglycine SCHEMBL3059831 0.84 CYP2D6 (0.59) CYP2D6MAPK1SMN1; SMN2TSHRALDH1A1
Phenylglycine SCHEMBL305330 0.84 CYP2D6 (0.59) CYP2D6MAPK1SMN1; SMN2TSHRALDH1A1
Isopropylamine SCHEMBL2350740 0.84 CYP2D6 (0.53) CYP2D6MAPK1SMN1; SMN2TSHRALDH1A1
SCHEMBL20853608 0.84 ALDH1A1 (0.52) CYP2D6MAPK1SMN1; SMN2TSHRALDH1A1
SCHEMBL1274859 0.82 CYP2D6 (0.51) CYP2D6MAPK1SMN1; SMN2TSHRALDH1A1
Sulfuric Acid SCHEMBL4454713 0.82 ALDH1A1 (0.53) ALDH1A1LMNAKDM4EMAPTTDP1

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-5663360-A REACTING 3,4-DIMETHOXYAMPHETAMINE WITH 3-CHLOROMANDELIC ACID F.I.S. FABBRICA ITALIANA SINTETICI S.P.A. (IT) 1997-09-02 US disclosed