SCHEMBL3708636

SCHEMBL3708636

Cc1c(O)ccc(O)c1O

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TRPA1 O75762 3/20 0.46
ATM Q13315 1/20 0.46
TYR P14679 1/20 0.45
TDP1 Q9NUW8 2/20 0.42
ALDH1A1 P00352 2/20 0.42
PIM1 P11309 1/20 0.42
ADAMTS4 O75173 1/20 0.42
EGFR P00533 1/20 0.42
CA1 P00915 1/20 0.42
CA2 P00918 1/20 0.42
LMNA P02545 1/20 0.42
FYN P06241 1/20 0.42
MMP2 P08253 1/20 0.42
MMP9 P14780 1/20 0.42
HPGD P15428 1/20 0.42
ALOX15 P16050 1/20 0.42
MMP8 P22894 1/20 0.42
CA6 P23280 1/20 0.42
CDK2 P24941 1/20 0.42
MMP12 P39900 1/20 0.42

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
SCHEMBL31290749 1.00 TRPA1 (0.46) TRPA1ATMTYRTDP1ALDH1A1
SCHEMBL29457565 0.82 TRPA1 (0.53) TRPA1ATMTYRTDP1ALDH1A1
SCHEMBL68013 0.82 TRPA1 (0.53) TRPA1ATMTYRTDP1ALDH1A1
SCHEMBL11802995 0.81 ESR1 (0.46) TRPA1ATMTYRTDP1ALDH1A1
SCHEMBL29356524 0.81 TRPA1 (0.48) TRPA1ATMTYRTDP1ALDH1A1
SCHEMBL68586 0.81 TRPA1 (0.48) TRPA1ATMTDP1ALDH1A1PIM1
SCHEMBL21287 0.81 TRPA1 (0.48) TRPA1ATMTYRTDP1ALDH1A1
SCHEMBL30925076 0.81 TRPA1 (0.48) TRPA1ATMTDP1ALDH1A1PIM1
SCHEMBL1136903 0.79 TRPA1 (0.46) TRPA1ATMTYRTDP1ALDH1A1
SCHEMBL315655 0.77 ALDH1A1 (0.46) TRPA1ATMTYRALDH1A1LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118136842-A Negative electrode material and preparation method and application thereof 湖南中科星城石墨有限公司 2024-06-04 CN claimed
CN-117466277-A Hard carbon precursor, hard carbon, preparation method of hard carbon and sodium battery 湖南中科星城石墨有限公司 2024-01-30 CN claimed
US-20120123171-A1 Catalytic reduction of lignin acids and substituted aliphatic carboxylic acid compounds CARTER TECHNOLOGIES (US) 2012-05-17 US claimed
WO-2025202454-A1 COSMETIC USES OF HYACINTHUS EXTRACTS LUCAS MEYER COSMETICS (FR) 2025-10-02 WO disclosed
EP-4565195-A1 LIGHT-MODULATING COSMETIC COMPOSITIONS AND USES THEREOF Lucas Meyer Cosmetics (FR) 2025-06-11 EP disclosed
WO-2025062101-A1 CITRUS AURANTIUM EXTRACT AND USE THEREOF AS COSMETIC AGENT LUCAS MEYER COSMETICS (FR) 2025-03-27 WO disclosed
EP-4499035-A1 <SMALLCAPS/>? ? ?MELALEUCA ALTERNIFOLIA? ? ? ? ?EXTRACT AND COSMETIC USES THEREOF Lucas Meyer Cosmetics (FR) 2025-02-05 EP disclosed
EP-4499028-A1 COSMETIC USE OF A LAVANDIN EXTRACT AS A PROTECTIVE OR ANTI-FATIGUE COSMETIC AGENT Lucas Meyer Cosmetics (FR) 2025-02-05 EP disclosed
CN-118136842-A Negative electrode material and preparation method and application thereof 湖南中科星城石墨有限公司 2024-06-04 CN disclosed
WO-2024030474-A1 LIGHT-MODULATING COSMETIC COMPOSITIONS AND USES THEREOF LUCAS MEYER COSMETICS SAS (FR) 2024-02-08 WO disclosed
CN-117466277-A Hard carbon precursor, hard carbon, preparation method of hard carbon and sodium battery 湖南中科星城石墨有限公司 2024-01-30 CN disclosed
EP-0241664-A1 Process for preparing substituted trihydroxybenzenes Degussa Aktiengesellschaft (DE) 1987-10-21 EP disclosed
EP-0032062-B1 HIGH-MOLECULAR-WEIGHT NOVOLAK SUBSTITUTED PHENOLIC RESINS AND THEIR PREPARATION MITSUI PETROCHEMICAL INDUSTRIES, LTD. (JP) 1985-04-03 EP disclosed
US-4345054-A High-molecular-weight novolak types substituted phenolic resins and process for preparation thereof MITSUI PETROCHEMICAL INDUSTRIES, LTD. (JP) 1982-08-17 US disclosed
EP-0032062-A2 High-molecular-weight novolak substituted phenolic resins and their preparation MITSUI PETROCHEMICAL INDUSTRIES, LTD. (JP) 1981-07-15 EP disclosed
EP-0000165-B1 PROCESS FOR PREPARING PURE 2-HYDROXYBENZYL ALCOHOL AND PURE 4-HYDROXYBENZYL ALCOHOL OR A MIXTURE OF BOTH HYDROXYBENZYL ALCOHOLS HAARMANN & REIMER GMBH (DE) 1981-06-03 EP 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
US-4192959-A COUNTERCURRENT EXTRACTION HAARMANN & REIMER (DE) 1980-03-11 US disclosed
EP-0000165-A1 Process for preparing pure 2-hydroxybenzyl alcohol and pure 4-hydroxybenzyl alcohol or a mixture of both hydroxybenzyl alcohols HAARMANN & REIMER GMBH (DE) 1979-01-10 EP disclosed
US-3987109-A POLYMERIZATION OF POLYFUNCTIONAL PHENOLS UNIVERSAL OIL PRODUCTS COMPANY (US) 1976-10-19 US disclosed