Diphenylmethanol

Diphenylmethanol

SCHEMBL5050461

CCO.OC(c1ccccc1)c1ccccc1

nearest known ligand 0.58

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Known targets — ChEMBL curated mechanism

MMP1MMP13MMP7MMP8polrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Diphenylmethanol. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
LMNA P02545 2/20 0.58
SMN1; SMN2 Q16637 1/20 0.50
L3MBTL1 Q9Y468 2/20 0.47
KDM4E B2RXH2 3/20 0.46
ALDH1A1 P00352 1/20 0.46
TRPA1 O75762 4/20 0.45
ATM Q13315 1/20 0.44
ADRA2A P08913 1/20 0.44
ADRA2C P18825 1/20 0.44
NPSR1 Q6W5P4 1/20 0.44
HIF1A Q16665 1/20 0.44
MEN1 O00255 1/20 0.44
MAPT P10636 1/20 0.44
CYP2C9 P11712 1/20 0.44
KMT2A Q03164 1/20 0.44
AOC3 Q16853 1/20 0.44
POLB P06746 1/20 0.44

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
Diphenylmethanol SCHEMBL28193469 0.92 LMNA (0.61) LMNASMN1; SMN2L3MBTL1KDM4EALDH1A1
Diphenylmethanol SCHEMBL10868602 0.86 SMN1; SMN2 (0.61) LMNASMN1; SMN2L3MBTL1KDM4EADRA2A
Diphenylmethanol SCHEMBL41571 0.86 SMN1; SMN2 (0.61) LMNASMN1; SMN2L3MBTL1KDM4EADRA2A
Diphenylmethanol SCHEMBL11564700 0.86 SMN1; SMN2 (0.61) LMNASMN1; SMN2L3MBTL1KDM4EADRA2A
Diphenylmethanol SCHEMBL6434457 0.86 SMN1; SMN2 (0.61) LMNASMN1; SMN2L3MBTL1KDM4EADRA2A
Diphenylmethanol SCHEMBL11393715 0.83 LMNA (0.52) LMNASMN1; SMN2L3MBTL1KDM4EATM
Diphenylmethanol SCHEMBL9324200 0.83 SMN1; SMN2 (0.58) LMNASMN1; SMN2L3MBTL1KDM4EADRA2A
Diphenylmethanol SCHEMBL8164003 0.83 SMN1; SMN2 (0.58) LMNASMN1; SMN2L3MBTL1KDM4EADRA2A
Diphenylmethanol SCHEMBL15641329 0.83 SMN1; SMN2 (0.58) LMNASMN1; SMN2L3MBTL1KDM4EADRA2A
SCHEMBL8671295 0.83 SMN1; SMN2 (0.58) LMNASMN1; SMN2L3MBTL1KDM4EADRA2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4736015-A FROM DI-(ORTETRA) ESTER OF BENZHYDROL 3,3*,4,4*-TETRACARBOXYLIC ACID AND AROMATIC DIAMINE INSTITUT FRANCAIS DU PETROLE (FR) 1988-04-05 US claimed
EP-1873156-A1 Process for the preparation of 6-[[(alkoxy)carbonyl]amino]-9H-Purine-9-acetic acid and 4-[(alkoxycarbonyl)amino]-2-oxo-1(2H)-Pyrimidineacetic acid derivatives as synthons for the synthesis of peptide nucleic acids PerSeptive Biosystems, Inc. (US) 2008-01-02 EP disclosed
EP-0736027-B1 GUANINE SYNTHONS FOR PEPTIDE NUCLEIC ACID SYNTHESIS AND METHOD FOR PRODUCTION PERSEPTIVE BIOSYSTEMS INC (US) 2002-05-29 EP disclosed
US-6172226-B1 Synthons for the synthesis and deprotection of peptide nucleic acids under mild conditions PERSEPTIVE BIOSYSTEMS, INC. 2001-01-09 US disclosed
EP-0840736-A1 IMPROVED SYNTHONS FOR THE SYNTHESIS AND DEPROTECTION OF PEPTIDE NUCLEIC ACIDS UNDER MILD CONDITIONS PerSeptive Biosystems, Inc. (US) 1998-05-13 EP disclosed
WO-1996040685-A1 IMPROVED SYNTHONS FOR THE SYNTHESIS AND DEPROTECTION OF PEPTIDE NUCLEIC ACIDS UNDER MILD CONDITIONS PERSEPTIVE BIOSYSTEMS, INC. (US) 1996-12-19 WO disclosed
EP-0736027-A1 GUANINE SYNTHONS FOR PEPTIDE NUCLEIC ACID SYNTHESIS AND METHOD FOR PRODUCTION PERSEPTIVE BIOSYSTEMS, INC. (US) 1996-10-09 EP disclosed
WO-1995017403-A1 GUANINE SYNTHONS FOR PEPTIDE NUCLEIC ACID SYNTHESIS AND METHOD FOR PRODUCTION PERSEPTIVE BIOSYSTEMS, INC. (US) 1995-06-29 WO disclosed