P-Cresol

P-Cresol

SCHEMBL28410048

Cc1ccc(O)cc1.NCCO

nearest known ligand 0.65

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

MPL

The experimentally established mechanism targets of P-Cresol. 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
▸ ACHE P22303 2/20 0.65
▸ ALDH1A1 P00352 5/20 0.46
▸ KDM4E B2RXH2 3/20 0.46
▸ TAAR1 Q96RJ0 2/20 0.46
▸ L3MBTL1 Q9Y468 2/20 0.46
▸ BACE1 P56817 2/20 0.46
▸ CYP1A2 P05177 1/20 0.46
▸ CYP2A6 P11509 1/20 0.46
▸ HTR1A P08908 1/20 0.46
▸ ADRA2A P08913 1/20 0.46
▸ SLC6A2 P23975 1/20 0.46
▸ CYP2C19 P33261 1/20 0.46
▸ HTR3A P46098 1/20 0.46
▸ BLM P54132 3/20 0.45
▸ KMT2A Q03164 3/20 0.45
▸ MAPT P10636 3/20 0.45
▸ MEN1 O00255 2/20 0.45
▸ HPGD P15428 2/20 0.45
▸ ALOX15 P16050 2/20 0.45
▸ HSD17B10 Q99714 2/20 0.45

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 SCHEMBL11759332 0.87 ALDH1A1 (0.57) ALDH1A1KDM4ETAAR1L3MBTL1BACE1
P-Cresol SCHEMBL9478964 0.83 ACHE (0.62) ACHEALDH1A1KDM4ETAAR1L3MBTL1
P-Cresol SCHEMBL8158679 0.81 ACHE (0.77) ACHEALDH1A1KDM4EL3MBTL1CYP1A2
P-Cresol SCHEMBL1127979 0.81 ACHE (0.87) ACHEALDH1A1KDM4EL3MBTL1CYP1A2
P-Xylene SCHEMBL28199191 0.81 ACHE (1.00) ACHEALDH1A1KDM4EL3MBTL1CYP1A2
P-Cresol SCHEMBL375 0.81 — —
P-Cresol SCHEMBL11263098 0.81 ACHE (1.00) ACHEALDH1A1KDM4EL3MBTL1CYP1A2
P-Cresol SCHEMBL9726112 0.81 ACHE (1.00) ACHEALDH1A1KDM4EL3MBTL1CYP1A2
P-Cresol SCHEMBL960690 0.81 ACHE (1.00) ACHEALDH1A1KDM4EL3MBTL1CYP1A2
P-Cresol SCHEMBL29774950 0.79 ACHE (0.56) ACHEALDH1A1KDM4ETAAR1L3MBTL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111269328-A Temperature response type eutectic solvent and extraction method of ganoderma lucidum polysaccharide 中国农业科学院麻类研究所 2020-06-12 — — CN disclosed
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