Biphenyl

Biphenyl

SCHEMBL10944895

Br.CCCC.P.c1ccc(-c2ccccc2)cc1

nearest known ligand 0.56

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHEADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3APH1AAPH1BCHRM2CHRM3EZH2GRIN2AHTR1AHTR1BHTR1DHTR1FHTR3ANCSTNP2RY12PSEN1PSEN2PSENENSIGMAR1SLC6A2SLC6A3SLC6A4

The experimentally established mechanism targets of Biphenyl. 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
SLC6A4 known ✓ P31645 1/20 0.43
ALDH1A1 P00352 4/20 0.56
SMN1; SMN2 Q16637 4/20 0.46
HPGD P15428 3/20 0.46
L3MBTL1 Q9Y468 2/20 0.46
MAPT P10636 4/20 0.44
SLC22A2 O15244 1/20 0.43
SLC22A1 O15245 1/20 0.43
SLC22A3 O75751 1/20 0.43
TP53 P04637 1/20 0.43
TAAR1 Q96RJ0 3/20 0.42
HSD17B10 Q99714 2/20 0.41
CYP1A2 P05177 2/20 0.41
MAPK1 P28482 1/20 0.41
CYP3A4 P08684 1/20 0.41
TDP1 Q9NUW8 1/20 0.41
NOTUM Q6P988 1/20 0.41
MMP3 P08254 1/20 0.41
BCL2L1 Q07817 1/20 0.41
TSHR P16473 1/20 0.40

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
Biphenyl SCHEMBL967556 0.94 ALDH1A1 (0.64) ALDH1A1SMN1; SMN2HPGDL3MBTL1MAPT
Biphenyl SCHEMBL22500791 0.90 ALDH1A1 (0.60) ALDH1A1SMN1; SMN2HPGDL3MBTL1MAPT
Biphenyl SCHEMBL7043290 0.90 ALDH1A1 (0.60) ALDH1A1SMN1; SMN2HPGDL3MBTL1MAPT
Biphenyl SCHEMBL4606121 0.90 ALDH1A1 (0.60) ALDH1A1SMN1; SMN2HPGDL3MBTL1MAPT
Biphenyl SCHEMBL9194626 0.88 ALDH1A1 (0.56) ALDH1A1SMN1; SMN2HPGDL3MBTL1MAPT
Biphenyl SCHEMBL16196748 0.85 ALDH1A1 (0.53) ALDH1A1SMN1; SMN2HPGDL3MBTL1MAPT
Biphenyl SCHEMBL323849 0.83 ALDH1A1 (0.69) ALDH1A1SMN1; SMN2HPGDL3MBTL1MAPT
Biphenyl SCHEMBL28142950 0.83 ALDH1A1 (0.82) ALDH1A1SMN1; SMN2MAPTSLC22A2SLC22A1
Biphenyl SCHEMBL15347228 0.81 ALDH1A1 (0.56) ALDH1A1SMN1; SMN2HPGDL3MBTL1MAPT
Biphenyl SCHEMBL5868585 0.81 ALDH1A1 (0.56) ALDH1A1SMN1; SMN2HPGDL3MBTL1MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0101167-B1 PROCESS FOR HYDROXYLATING OLEFINS IN THE PRESENCE OF AN OSMIUM CONTAINING CATALYST AND ORGANIC HALOGENATED HYDROCARBON CO-CATALYST EXXON RESEARCH AND ENGINEERING COMPANY (US) 1985-12-18 EP disclosed
EP-0053023-B1 HYDROXYLATION OF OLEFINS EXXON RESEARCH AND ENGINEERING COMPANY (US) 1985-04-17 EP disclosed
US-4482763-A Process for hydroxylating olefins in the presence of an osmium containing catalyst and organic halogenated hydrocarbon co-catalyst EXXON RESEARCH & ENGINEERING CO. (US) 1984-11-13 US disclosed
EP-0101167-A1 Process for hydroxylating olefins in the presence of an osmium containing catalyst and organic halogenated hydrocarbon co-catalyst EXXON RESEARCH AND ENGINEERING COMPANY (US) 1984-02-22 EP disclosed
US-4393253-A Hydroxylation of olefins EXXON RESEARCH & ENGINEERING CO. (US) 1983-07-12 US disclosed