SCHEMBL67576

SCHEMBL67576

Cc1cc(O)cc(O)c1O

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP3A4 P08684 5/20 0.50
ACHE P22303 2/20 0.50
CHRM1 P11229 1/20 0.50
ALOX15 P16050 1/20 0.50
MAOA P21397 1/20 0.50
TBXA2R P21731 1/20 0.50
ADRA1A P35348 1/20 0.50
HTR2B P41595 1/20 0.50
SELL P14151 1/20 0.48
SELP P16109 1/20 0.48
SELE P16581 1/20 0.48
CA1 P00915 1/20 0.48
CA2 P00918 1/20 0.48
ALDH1A1 P00352 2/20 0.43
TDP1 Q9NUW8 2/20 0.42
EGFR P00533 1/20 0.42
ERBB2 P04626 1/20 0.42
SMN1; SMN2 Q16637 1/20 0.42
TRPA1 O75762 1/20 0.42
MEN1 O00255 3/20 0.41

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
SCHEMBL22339 0.84 CA1 (0.65) CYP3A4ACHECHRM1ALOX15MAOA
Methane SCHEMBL8857034 0.81 CA1 (0.61) CYP3A4ACHECHRM1ALOX15MAOA
Ethane SCHEMBL27680247 0.81 CA1 (0.61) CYP3A4ACHECHRM1ALOX15MAOA
Ethane SCHEMBL27964241 0.78 SELL (0.56) CYP3A4ACHESELLSELPSELE
SCHEMBL67497 0.77 BACE1 (0.54) CYP3A4ALOX15SELLSELPSELE
SCHEMBL70189 0.77 SELL (0.72) ACHESELLSELPSELECA1
SCHEMBL23883044 0.77 CYP3A4 (0.50) CYP3A4ACHECHRM1ALOX15MAOA
SCHEMBL29429337 0.77 CYP3A4 (0.50) CYP3A4ACHECHRM1ALOX15MAOA
SCHEMBL69242 0.77 CYP3A4 (0.50) CYP3A4ACHECHRM1ALOX15MAOA
Propane SCHEMBL28325854 0.77 CA1 (0.55) CYP3A4ACHECHRM1ALOX15MAOA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4563188-A SHADES OF GREEN L'OREAL (FR) 1986-01-07 US claimed
US-4333730-A HAIR DYES SOCIETE ANONYME DITE: L'OREAL (FR) 1982-06-08 US claimed
US-4330292-A CONTAINING AN OXIDATION BASE L'OREAL (FR) 1982-05-18 US claimed
EP-4400501-A1 NOVEL COMPOUND AND ORGANIC LIGHT EMITTING DEVICE COMPRISING SAME LG Chem, Ltd. (KR) 2024-07-17 EP disclosed
US-20180105729-A1 WINTERIZING COMPOSITIONS FOR SULFUR SCAVENGERS AND METHODS FOR MAKING AND USING SAME THE LUBRIZOL CORPORATION 2018-04-19 US disclosed
EP-3268444-A1 WINTERIZING COMPOSITIONS FOR SULFUR SCAVENGERS AND METHODS FOR MAKING AND USING SAME Lubrizol Oilfield Solutions, Inc. (US) 2018-01-17 EP disclosed
EP-2708223-B1 DYEING AGENT AND USE FOR SAME AMANO ENZYME INC (JP) 2017-02-01 EP disclosed
CN-103517703-B Stain and application thereof 天野酶制品株式会社 2016-11-09 CN disclosed
WO-2016145172-A1 WINTERIZING COMPOSITIONS FOR SULFUR SCAVENGERS AND METHODS FOR MAKING AND USING SAME Lubrizol Oilfield Solutions, Inc. (US) 2016-09-15 WO disclosed
US-8946188-B2 Anti-microbial agents and uses thereof SLOAN-KETTERING INSTITUTE FOR CANCER RESEARCH (US) 2015-02-03 US disclosed
US-8740994-B2 Dyeing agent and use for same AMANO ENZYME INC. (JP) 2014-06-03 US disclosed
WO-1997023685-A1 ENZYMATIC METHOD FOR TEXTILE DYEING NOVO NORDISK BIOCHEM NORTH AMERICA, INC. (US) 1997-07-03 WO disclosed
EP-0367283-A2 Wet set additives for high resilience foam UNION CARBIDE CHEMICALS AND PLASTICS COMPANY INC. (a New York corporation) (US) 1990-05-09 EP disclosed
US-4888025-A 1-PHENOXY-3-AMINOPROPAN-2-OL L'OREAL (FR) 1989-12-19 US disclosed
US-4563188-A SHADES OF GREEN L'OREAL (FR) 1986-01-07 US disclosed
US-4466806-A Dyeing compositions containing 3-amino-4-nitroanisole derivatives and their use in dyeing keratin fibres as well as certain new said derivatives L'OREAL (FR) 1984-08-21 US disclosed
US-4432769-A MADE BY REACTING 3-AMINO-4-NITRO-CHLOROBENZENE WITH GLYCEROL L'OREAL (FR) 1984-02-21 US disclosed
US-4333730-A HAIR DYES SOCIETE ANONYME DITE: L'OREAL (FR) 1982-06-08 US disclosed
US-4330292-A CONTAINING AN OXIDATION BASE L'OREAL (FR) 1982-05-18 US disclosed
US-4205188-A CONDENSATION OF PHENOL AND FORMALDEHYDE AND REMOVAL OF EXCESS PHENOL BY SOLVENT EXTRACTION THE DOW CHEMICAL COMPANY (US) 1980-05-27 US disclosed