SCHEMBL207038

SCHEMBL207038

Cc1ccc(O)c(C)c1C

nearest known ligand 0.57

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ TRPA1 O75762 4/20 0.57
▸ ATM Q13315 1/20 0.57
▸ TP53 P04637 1/20 0.43
▸ TDP1 Q9NUW8 1/20 0.43
▸ SCN5A Q14524 1/20 0.41
▸ HTR1D P28221 1/20 0.40
▸ HTR1B P28222 1/20 0.40
▸ TSHR P16473 1/20 0.40
▸ CASP1 P29466 1/20 0.40
▸ PDE10A Q9Y233 1/20 0.40
▸ ESR1 P03372 3/20 0.39
▸ ESR2 Q92731 2/20 0.39
▸ KDM4E B2RXH2 3/20 0.39
▸ MAPK1 P28482 3/20 0.39
▸ MAPT P10636 2/20 0.39
▸ ALDH1A1 P00352 1/20 0.39
▸ CYP1A2 P05177 1/20 0.39
▸ CYP3A4 P08684 1/20 0.39
▸ CYP2D6 P10635 1/20 0.39
▸ G6PD P11413 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
SCHEMBL30388902 1.00 TRPA1 (0.57) TRPA1ATMTP53TDP1SCN5A
Ammonia Solution, Strong SCHEMBL1065150 0.97 TRPA1 (0.55) TRPA1ATMTP53TDP1SCN5A
Phosphine SCHEMBL1067227 0.97 TRPA1 (0.55) TRPA1ATMTP53TDP1SCN5A
Hydrochloric Acid SCHEMBL6039932 0.94 TRPA1 (0.52) TRPA1ATMTP53TDP1SCN5A
Dimethylamine SCHEMBL675006 0.92 TRPA1 (0.50) TRPA1ATMTP53TDP1SCN5A
Alcohol SCHEMBL28492687 0.89 TRPA1 (0.48) TRPA1ATMTP53TDP1SCN5A
SCHEMBL16852427 0.89 TRPA1 (0.48) TRPA1ATMTP53TDP1SCN5A
Acetic Acid SCHEMBL6557428 0.87 TRPA1 (0.46) TRPA1ATMTP53TDP1SCN5A
Formic Acid SCHEMBL9009952 0.87 TRPA1 (0.46) TRPA1ATMTP53TDP1SCN5A
SCHEMBL11865245 0.87 TRPA1 (0.46) TRPA1ATMTP53TDP1SCN5A

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

Appears in 4107 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4416124-B1 PROCESS FOR PRODUCING CRESOL AND XYLENE UOP LLC (US) 2025-09-03 — — EP claimed
EP-4598350-A1 CONCENTRATED ANTIMICROBIAL SOLUTIONS CONTAINING SPARINGLY SOLUBLE ANTIMICROBIAL AGENTS Virox Technologies Inc. (CA) 2025-08-13 — — EP claimed
CN-120193416-A Aqueous dip bath compound for treating reinforcing inserts, use thereof, and method for producing adhesive reinforcing inserts EMS化学股份公司 2025-06-24 — — CN claimed
CN-120025230-A Method for recycling phenolic compounds from epoxy resin-based waste in high yield 四川大学 2025-05-23 — — CN claimed
CN-119717395-A Chemically amplified positive resist composition and use thereof 台湾永光化学工业股份有限公司 2025-03-28 — — CN claimed
CN-118184489-B Method for preparing trimethylhydroquinone by using trimethylhydroquinone synthesis byproducts 巨野百林化学有限公司 2025-03-04 — — CN claimed
CN-119490388-A Method for separating and obtaining phenolic substances from phenol-containing coal tar 煤炭科学技术研究院有限公司 2025-02-21 — — CN claimed
CN-119431113-A Method for refining 2,3, 5-tricresyl and 3-methyl-5-ethylphenol from trimethylphenol mixture 煤炭科学技术研究院有限公司 2025-02-14 — — CN claimed
CN-119431115-A Impurity removing method for mixed phenol extracted from coal tar 煤炭科学技术研究院有限公司 2025-02-14 — — CN claimed
CN-119335815-A Positive photoresist composition and method for forming photoresist pattern 天津久日半导体材料有限公司 2025-01-21 — — CN claimed
EP-0034648-A2 A method for the alkoxylation of alkanols in the presence of strontium-containing catalysts and promoters Conoco Phillips Company (US) 1981-09-02 — — EP claimed
EP-0033760-A1 A method for the alkoxylation of alkanols Conoco Phillips Company (US) 1981-08-19 — — EP claimed
US-4267392-A TWO-STEP SEPARATION AND PURIFICATION BY PREFERENTIAL COMPLEXING OF FIRST P-CRESOL THEN M-CRESOL WITH A METAL HALIDE; DECOMPOSITION OF THE SOLID COMPLEX KOPPERS COMPANY, INC. (US) 1981-05-12 — — US claimed
US-4267389-A PREFERENTIAL COMPLEXING WITH AN ANHYDROUS METAL HALIDE; REMOVAL; DECOMPOSITION KOPPERS COMPANY, INC. (US) 1981-05-12 — — US claimed
US-4250335-A USING DIBUTYL ETHER AND WATER TO SEPARATE THE 2,3,5-P-QUINONE INTERMEDIATE, THE COBALT COMPLEX CATALYST, AND THE DIMETHYLFORMAMIDE SOLVENT; LIQUID PHASE HYDROGENATION SHELL OIL COMPANY (US) 1981-02-10 — — US claimed
US-4234733-A PHENOL, ALIPHATIC ESTER OR ETHER, CARBON MONOXIDE MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 1980-11-18 — — US claimed
US-4151183-A OXIDATION OF TRIMETHYLPHENOL IN PRESENCE OF COMPLEX COBALT COMPOUND RHONE POULENC, S.A. (FR) 1979-04-24 — — US claimed
US-4125560-A Aromatic amines synthesis process and products resulting from application of this process UNIVERSITE LIBRE DE BRUXELLES FACULTE DES SCIENCES APPLIQUEES (BE) 1978-11-14 — — US claimed
US-4024195-A CATALYST, ALCOHOL MITSUBISHI GAS CHEMICAL COMPANY, INC. (JA) 1977-05-17 — — US claimed
US-3971832-A FROM A PHENOL AND METHANOL, TRI-MANGANESE TETROXIDE CATALYST MITSUBISHI PETROCHEMICAL COMPANY LIMITED (JA) 1976-07-27 — — US claimed
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