1-Naphthol

1-Naphthol

SCHEMBL4196679

Oc1cccc2ccccc12.[Ti]

nearest known ligand 0.94

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 2/20 0.94
IDO1 P14902 1/20 0.55
PTPN22 Q9Y2R2 1/20 0.54
HSD17B10 Q99714 5/20 0.52
TDP1 Q9NUW8 3/20 0.52
TSHR P16473 3/20 0.52
HPGD P15428 3/20 0.52
MAPT P10636 2/20 0.52
ALOX15 P16050 2/20 0.52
RECQL P46063 2/20 0.52
APP P05067 1/20 0.52
THRB P10828 1/20 0.52
CASP1 P29466 1/20 0.52
SNCA P37840 1/20 0.52
NQO2 P16083 1/20 0.52
KDM4E B2RXH2 2/20 0.52
PLAU P00749 1/20 0.52
MAPKAPK2 P49137 1/20 0.52
CTDSP1 Q9GZU7 1/20 0.52
ALDH1A1 P00352 3/20 0.50

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
1-Naphthol SCHEMBL27527869 1.00 CYP1A2 (0.94) CYP1A2IDO1PTPN22HSD17B10TDP1
1-Naphthol SCHEMBL10486461 0.97 CYP1A2 (1.00) CYP1A2IDO1PTPN22HSD17B10TDP1
1-Naphthol SCHEMBL3416 0.97 CYP1A2 (1.00) CYP1A2IDO1PTPN22HSD17B10TDP1
1-Naphthol SCHEMBL29767730 0.97 CYP1A2 (1.00) CYP1A2IDO1PTPN22HSD17B10TDP1
1-Naphthol SCHEMBL273260 0.97 CYP1A2 (1.00) CYP1A2IDO1PTPN22HSD17B10TDP1
1-Naphthol SCHEMBL11247168 0.94 CYP1A2 (0.94) CYP1A2IDO1PTPN22HSD17B10TDP1
1-Naphthol SCHEMBL3924043 0.94 CYP1A2 (0.94) CYP1A2IDO1PTPN22HSD17B10TDP1
1-Naphthol SCHEMBL11295882 0.94 CYP1A2 (0.94) CYP1A2IDO1PTPN22HSD17B10TDP1
1-Naphthol SCHEMBL21490911 0.94 CYP1A2 (0.94) CYP1A2IDO1PTPN22HSD17B10TDP1
1-Naphthol SCHEMBL9850309 0.94 CYP1A2 (0.94) CYP1A2IDO1PTPN22HSD17B10TDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-1068876-C Process for preparing chiral succinic acid derivatives HOFFMANN LA ROCHE (CH) 2001-07-25 CN claimed
CN-1177595-A Process for preparing chiral succinic acid derivatives HOFFMANN LA ROCHE (CH) 1998-04-01 CN claimed
CN-104788462-B Chiral polysubstituted 4-hydroxychroman compound, and preparation method and application thereof 中国科学院化学研究所 2017-02-08 CN disclosed
US-20090036441-A1 Indole Derivatives With Antitumor Activity CELL THERAPEUTICS EUROPE S.R.L. (IT) 2009-02-05 US disclosed
CN-101083983-A Indole derivatives with antitumor activity CELL THERAPEUTICS EUROPE SRL (IT) 2007-12-05 CN disclosed
CN-1308066-A Preparation of chiral succinic acid derivative HOFFMANN LA ROCHE (CH) 2001-08-15 CN disclosed
CN-1068876-C Process for preparing chiral succinic acid derivatives HOFFMANN LA ROCHE (CH) 2001-07-25 CN disclosed
CN-1177595-A Process for preparing chiral succinic acid derivatives HOFFMANN LA ROCHE (CH) 1998-04-01 CN disclosed
CN-1066075-A PROCESS FOR PREPARING POLYOLEFINS NIPPON OIL CO LTD (JP) 1992-11-11 CN disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20090036441-A1 Indole Derivatives With Antitumor Activity IDO1, IDO2, INMT CYP1A2 259/4885IDO1 1/4885PTPN22 4535/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.