Resorcinol

Resorcinol

SCHEMBL8052940

Cc1ccc(OP(=O)(Oc2ccc(C)cc2)OP(=O)(Oc2ccc(C)cc2)Oc2ccc(C)cc2)cc1.Oc1cccc(O)c1

nearest known ligand 0.58

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP3A4 P08684 4/20 0.58
TSHR P16473 2/20 0.58
MEN1 O00255 4/20 0.45
KMT2A Q03164 4/20 0.45
ACHE P22303 1/20 0.42
LMNA P02545 3/20 0.40
ALDH1A1 P00352 2/20 0.40
CA12 O43570 1/20 0.40
CA2 P00918 1/20 0.40
CA5A P35218 1/20 0.40
CA9 Q16790 1/20 0.40
HSD17B10 Q99714 1/20 0.40
CA14 Q9ULX7 1/20 0.40
CA5B Q9Y2D0 1/20 0.40
MAPK1 P28482 1/20 0.40
TDP1 Q9NUW8 1/20 0.40
MAPT P10636 1/20 0.39
POLB P06746 1/20 0.38
GAA P10253 1/20 0.38
MMP1 P03956 1/20 0.38

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
SCHEMBL9308791 0.87 CYP3A4 (0.63) CYP3A4TSHRMEN1KMT2AACHE
Hydroquinone SCHEMBL5087178 0.86 CYP3A4 (0.67) CYP3A4TSHRMEN1KMT2AACHE
Resorcinol SCHEMBL28304272 0.85 CYP3A4 (0.50) CYP3A4TSHRMEN1KMT2AACHE
Resorcinol SCHEMBL122252 0.84 SRC (0.48) CYP3A4LMNAALDH1A1CA12CA2
Resorcinol SCHEMBL27618448 0.84 SRC (0.48) CYP3A4LMNAALDH1A1CA12CA2
SCHEMBL5698269 0.84 CYP3A4 (0.82) CYP3A4TSHRMEN1KMT2AACHE
Phenol SCHEMBL27766616 0.81 CYP3A4 (0.70) CYP3A4TSHRMEN1KMT2AACHE
SCHEMBL34838 0.78 CYP3A4 (0.79) CYP3A4TSHRMEN1KMT2AACHE
Resorcinol SCHEMBL14939224 0.78 CYP3A4 (0.41) CYP3A4MEN1KMT2AACHELMNA
SCHEMBL133405 0.77 CYP3A4 (0.76) CYP3A4TSHRMEN1KMT2ALMNA

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