Resorcinol

Resorcinol

SCHEMBL8054902

Cc1cccc(OP(=O)(Oc2cccc(C)c2C)OP(=O)(Oc2cccc(C)c2C)Oc2cccc(C)c2C)c1C.Oc1cccc(O)c1

nearest known ligand 0.54

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 3/20 0.54
ALDH1A1 P00352 2/20 0.39
LMNA P02545 3/20 0.38
CYP3A4 P08684 2/20 0.38
CA12 O43570 1/20 0.38
CA2 P00918 1/20 0.38
CA5A P35218 1/20 0.38
CA9 Q16790 1/20 0.38
HSD17B10 Q99714 1/20 0.38
CA14 Q9ULX7 1/20 0.38
CA5B Q9Y2D0 1/20 0.38
POLB P06746 4/20 0.37
RAB9A P51151 4/20 0.37
L3MBTL1 Q9Y468 1/20 0.37
GAA P10253 1/20 0.37
MAPK1 P28482 1/20 0.37
HTT P42858 1/20 0.37
MEN1 O00255 2/20 0.36
KMT2A Q03164 2/20 0.36
TDP1 Q9NUW8 1/20 0.36

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
Hydroquinone SCHEMBL5083118 0.90 MAPT (0.57) MAPTALDH1A1LMNACYP3A4POLB
Resorcinol SCHEMBL28688197 0.86 MAPT (0.56) MAPTALDH1A1LMNACYP3A4CA12
Resorcinol SCHEMBL729446 0.86 MAPT (0.56) MAPTALDH1A1LMNACYP3A4CA12
Resorcinol SCHEMBL28548452 0.85 MAPT (0.44) MAPTALDH1A1LMNACYP3A4CA12
Resorcinol SCHEMBL14939224 0.82 CYP3A4 (0.41) MAPTALDH1A1LMNACYP3A4CA12
Bisphenol A SCHEMBL29669605 0.81 MAPT (0.48) MAPTALDH1A1LMNACYP3A4HSD17B10
SCHEMBL108985 0.81 MAPT (0.71) MAPTALDH1A1LMNACYP3A4POLB
Orcinol SCHEMBL27934275 0.77 MAPT (0.53) MAPTALDH1A1LMNAPOLBRAB9A
SCHEMBL6814025 0.76 MAPT (0.65) MAPTALDH1A1LMNACYP3A4POLB
Phenol SCHEMBL2452431 0.76 MAPT (0.56) MAPTALDH1A1LMNACYP3A4HSD17B10

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6075158-A CATALYTIC REACTING A TRIARYL PHOSPHATE WITH AN ALCOHOL IN THE PRESENCE OF A BASE TO PRODUCE THE PHOSPHATE ESTER PRODUCT GREAT LAKES CHEMICAL CORPORATION (US) 2000-06-13 US disclosed
EP-0775147-B1 TRANSESTERIFICATION PROCESS FMC CORP UK LTD (GB) 1999-12-15 EP disclosed
EP-0775147-A1 TRANSESTERIFICATION PROCESS FMC Corporation (UK) Limited (GB) 1997-05-28 EP disclosed
WO-1996005208-A1 TRANSESTERIFICATION PROCESS FMC CORPORATION (UK) LIMITED (GB) 1996-02-22 WO disclosed