Diphenylmethane

Diphenylmethane

SCHEMBL9099741

Cc1ccc(S(=O)(=O)O)cc1.c1ccc(Cc2ccccc2)cc1

nearest known ligand 0.54

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABL1BMXBRAFBTKCHRNA4CHRNB2CSNK1EEGFRERBB2F10FLT1FLT3FLT4IGF1RINSRITKJAK3KDRKITOPRM1PARP1PARP2PDGFRBPIK3CDRAF1RETSLC18A2TECTXKdacAdacBdacCftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Diphenylmethane. 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
SMN1; SMN2 Q16637 3/20 0.54
TSHR P16473 1/20 0.54
L3MBTL1 Q9Y468 2/20 0.53
CA12 O43570 2/20 0.53
CA9 Q16790 2/20 0.53
BCHE P06276 1/20 0.53
ACHE P22303 1/20 0.53
CYP1A2 P05177 1/20 0.53
CYP3A4 P08684 1/20 0.53
ATM Q13315 1/20 0.53
CYP2D6 P10635 2/20 0.51
MAPK1 P28482 1/20 0.51
MCHR1 Q99705 1/20 0.50
KMT2A Q03164 1/20 0.49
LMNA P02545 3/20 0.49
ALDH1A1 P00352 3/20 0.49
MAPT P10636 2/20 0.49
HTT P42858 2/20 0.49
KDM4E B2RXH2 1/20 0.49
TDP1 Q9NUW8 1/20 0.49

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
SCHEMBL6134088 0.90 CYP2C9 (0.50) SMN1; SMN2TSHRL3MBTL1CA12CA9
SCHEMBL3151100 0.88 TSHR (0.62) SMN1; SMN2TSHRCA12CA9CYP2D6
Benzyl Alcohol SCHEMBL1870759 0.87 TSHR (0.52) SMN1; SMN2TSHRL3MBTL1CA12CA9
N-Benzylmethylamine SCHEMBL20239926 0.86 CYP3A4 (0.59) SMN1; SMN2TSHRL3MBTL1CA12CA9
Toluene SCHEMBL180606 0.86 SMN1; SMN2 (0.65) SMN1; SMN2TSHRL3MBTL1CA12CA9
SCHEMBL932442 0.86 SMN1; SMN2 (0.73) SMN1; SMN2TSHRL3MBTL1CA12CA9
SCHEMBL13836876 0.86 SMN1; SMN2 (0.73) SMN1; SMN2TSHRL3MBTL1CA12CA9
Diphenylmethane SCHEMBL9099676 0.86 TSHR (0.73) SMN1; SMN2TSHRCA12CA9CYP3A4
Benzene SCHEMBL5085625 0.86 SMN1; SMN2 (0.64) SMN1; SMN2TSHRL3MBTL1CA12CA9
Benzylamine SCHEMBL5820436 0.86 BCHE (0.54) SMN1; SMN2TSHRL3MBTL1CA12CA9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11450445-B2 Electroconductive film and method for manufacturing electroconductive pattern TOKYO UNIVERSITY OF SCIENCE FOUNDATION (JP) 2022-09-20 US disclosed
US-20200303086-A1 ELECTROCONDUCTIVE FILM AND METHOD FOR MANUFACTURING ELECTROCONDUCTIVE PATTERN TOKYO UNIVERSITY OF SCIENCE FOUNDATION (JP) 2020-09-24 US disclosed
US-10720259-B2 Electroconductive film and method for manufacturing electroconductive pattern TOKYO UNIVERSITY OF SCIENCE FOUNDATION (JP) 2020-07-21 US disclosed
US-20170309363-A1 ELECTROCONDUCTIVE FILM AND METHOD FOR MANUFACTURING ELECTROCONDUCTIVE PATTERN TOKYO UNIVERSITY OF SCIENCE FOUNDATION (JP) 2017-10-26 US disclosed
US-5489501-A MIXTURES OF TWO COORDINATION COMPOUNDS WHICH REACT TO FORM NEW COORDINATION COMPOUND WHILE CAUSING VISIBLE COLOR CHANGES RICOH COMPANY, LTD. (JP) 1996-02-06 US disclosed
US-5446011-A Imagewise coloring when heating; mixture of n-substituted indole, aromatic polyhydroxy compound, carbonyl compound and an acid RICOH COMPANY, LTD. (JP) 1995-08-29 US disclosed