Phenol

Phenol

SCHEMBL3166162

Clc1ccc2cc(Cl)[nH]c2c1.Oc1ccccc1

nearest known ligand 0.51

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
DAO P14920 1/20 0.51
ALOX15 P16050 5/20 0.43
MEN1 O00255 3/20 0.41
KMT2A Q03164 3/20 0.41
KDM4E B2RXH2 2/20 0.41
ALDH1A1 P00352 2/20 0.41
MAPT P10636 2/20 0.41
TP53 P04637 1/20 0.41
CYP3A4 P08684 1/20 0.41
HPGD P15428 1/20 0.41
MAPK1 P28482 1/20 0.41
HSD17B10 Q99714 1/20 0.41
FTO Q9C0B1 1/20 0.41
RAB9A P51151 3/20 0.40
NPC1 O15118 2/20 0.40
LMNA P02545 1/20 0.40
CYP19A1 P11511 1/20 0.40
SMN1; SMN2 Q16637 1/20 0.40
F11 P03951 1/20 0.40
TSHR P16473 1/20 0.39

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
SCHEMBL30146944 0.85 DAO (0.55) DAOALOX15ALDH1A1HPGDHSD17B10
SCHEMBL7048502 0.85 DAO (0.55) DAOALOX15ALDH1A1HPGDHSD17B10
Phenol SCHEMBL10954832 0.74 CYP2A6 (0.74) ALOX15MEN1KMT2AKDM4EMAPT
SCHEMBL17022664 0.74 DAO (0.61) DAOALOX15ALDH1A1CYP3A4HPGD
SCHEMBL28280447 0.73 FGFR1 (0.49) MEN1KMT2AKDM4EALDH1A1MAPT
SCHEMBL10413632 0.71 KMT2A (0.74) DAOMEN1KMT2AKDM4EALDH1A1
SCHEMBL980499 0.71 AOC3 (0.54) DAOMEN1KMT2AKDM4EALDH1A1
SCHEMBL30041175 0.71 AOC3 (0.54) DAOMEN1KMT2AKDM4EALDH1A1
1,4-Dichlorobenzene SCHEMBL4557393 0.70 CA12 (0.69) ALOX15MEN1KMT2AMAPTMAPK1
SCHEMBL7489718 0.69 DAO (0.51) DAOALOX15ALDH1A1HPGDHSD17B10

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 22 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0369657-A2 Chromogenic substrate for esterase and immunoassay using same Becton, Dickinson and Company (US) 1990-05-23 EP claimed
CN-108477439-A Vegetable beverage of broccoli containing selenium and preparation method thereof 恩施土家族苗族自治州农业科学院 2018-09-04 CN disclosed
CN-107708440-A Fructus Monordicae extract without agricultural chemicals and preparation method thereof 莎罗雅株式会社 2018-02-16 CN disclosed
CN-106770241-B Detect test paper component of Vitamin C content and preparation method thereof in liquid food 张育宁 2018-02-06 CN disclosed
CN-103403174-B Enzymatic synthesis of active pharmaceutical ingredients and intermediates thereof 力奇制药公司 2017-10-27 CN disclosed
CN-106770241-A Test paper component of Vitamin C content and preparation method thereof in detection liquid food 张育宁 2017-05-31 CN disclosed
CN-103913440-A Detection method and reagent of enzyme activity of pyruvate dehydrogenase complex BEIJING HEXIN FEIFAN BIOTECHNOLOGY CO LTD 2014-07-09 CN disclosed
CN-103403174-A Enzymatic synthesis of active pharmaceutical ingredient and intermediates thereof LEK PHARMACEUTICALS 2013-11-20 CN disclosed
US-8278451-B2 Pseudoazulenyl nitrones THE FLORIDA INTERNATIONAL UNIVERSITY BOARD OF TRUSTEES (US) 2012-10-02 US disclosed
US-20100016349-A1 PSEUDOAZULENYL NITRONES THE FLORIDA INTERNATIONAL UNIVERSITY BOARD OF TRUSTEES (US) 2010-01-21 US disclosed
CN-101017134-A Spectrophotometry for testing activity of pyruvic acid dehydrogenase system UNIV HUAZHONG NORMAL (CN) 2007-08-15 CN disclosed
EP-0888290-B1 AZULENYL NITRONE SPIN TRAPPING AGENTS, METHODS OF MAKING AND USING SAME FLORIDA INTERNAT UNIVERSITY (US) 2006-12-27 EP disclosed
EP-0888290-A4 AZULENYL NITRONE SPIN TRAPPING AGENTS, METHODS OF MAKING AND USING SAME FLORIDA INTERNAT UNIVERSITY (US) 2004-08-18 EP disclosed
US-6291702-B1 AS AGENTS FOR TRAPPING AND IDENTIFYING FREE RADICAL SPECIES AND FIND USE AS EFFICIENT ANTIOXIDANTS IN PHYSICOCHEMICAL AND BIOLOGICAL SYSTEMS. FLORIDA INTERNATIONAL UNIVERSITY 2001-09-18 US disclosed
US-6197825-B1 EFFECTIVE AGENTS FOR TRAPPING AND IDENTIFYING FREE RADICAL SPECIES AND FIND USE AS EFFICIENT ANTIOXIDANTS IN PHYSICOCHEMICAL AND BIOLOGICAL SYSTEMS. DIAMAGNETIC NITRONE COMPOUND (THE ?SPIN TRAP?) REACTS WITH A TRANSIENT FREE FLORIDA INTERNATIONAL UNIVERSITY 2001-03-06 US disclosed
US-6083988-A AZULENYL NITRONES ARE EFFECTIVE AGENTS FOR TRAPPING AND IDENTIFYING FREE RADICALS AND FIND USE AS EFFICIENT ANTIOXIDANT IN PHYSICOCHEMICAL AND BIOLOGICAL SYSTEMS FLORIDA INTERNATIONAL UNIVERSITY 2000-07-04 US disclosed
EP-0888290-A1 AZULENYL NITRONE SPIN TRAPPING AGENTS, METHODS OF MAKING AND USING SAME Florida International University (US) 1999-01-07 EP disclosed
WO-1997019054-A9 AZULENYL NITRONE SPIN TRAPPING AGENTS, METHODS OF MAKING AND USING SAME 1997-08-07 WO disclosed
WO-1997019054-A1 AZULENYL NITRONE SPIN TRAPPING AGENTS, METHODS OF MAKING AND USING SAME FLORIDA INTERNATIONAL UNIVERSITY (US) 1997-05-29 WO disclosed
EP-0286434-A2 Method for the detection of bacteria and fungi CAMBRIDGE BIOSCIENCE CORPORATION (US) 1988-10-12 EP 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-20100016349-A1 PSEUDOAZULENYL NITRONES TXN2, NOX5, TXNRD2 DAO 1259/4885ALOX15 268/4885MEN1 3491/4885

“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.