Catechol

Catechol

SCHEMBL367675

Oc1ccccc1O.Oc1ccccc1O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ ALDH1A1 P00352 6/20 1.00
▸ CA2 P00918 6/20 1.00
▸ HPGD P15428 4/20 1.00
▸ TDP1 Q9NUW8 4/20 1.00
▸ CA4 P22748 4/20 1.00
▸ ALOX15 P16050 3/20 1.00
▸ LMNA P02545 3/20 1.00
▸ HSD17B10 Q99714 3/20 1.00
▸ KDM4E B2RXH2 3/20 1.00
▸ SMN1; SMN2 Q16637 3/20 1.00
▸ CA12 O43570 3/20 1.00
▸ CA14 Q9ULX7 3/20 1.00
▸ EGFR P00533 2/20 1.00
▸ FYN P06241 2/20 1.00
▸ MMP9 P14780 2/20 1.00
▸ RECQL P46063 2/20 1.00
▸ NPC1 O15118 2/20 1.00
▸ MAPT P10636 2/20 1.00
▸ CA3 P07451 2/20 1.00
▸ GMNN O75496 1/20 1.00

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
Catechol SCHEMBL11672589 1.00 ALDH1A1 (1.00) ALDH1A1CA2HPGDTDP1CA4
Catechol SCHEMBL29352716 1.00 — —
Catechol SCHEMBL30088487 1.00 — —
Catechol SCHEMBL18351 1.00 — —
Catechol SCHEMBL30944695 1.00 ALDH1A1 (1.00) ALDH1A1CA2HPGDTDP1CA4
Catechol SCHEMBL25313512 0.95 — —
Catechol SCHEMBL22028465 0.95 CA2 (0.91) ALDH1A1CA2HPGDTDP1CA4
Catechol SCHEMBL330099 0.95 — —
Catechol SCHEMBL20590982 0.95 — —
Catechol SCHEMBL20597824 0.95 — —

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2012114347-A1 SYNTHESIS OF CHIRAL SUBSTITUTED BENZENES AND RELATED AROMATIC COMPOUNDS CONTAINING 1,2 DIOLS PROTECTED AS DIACETAL GROUPS AVRA LABORATORIES PVT. LTD. (IN) 2012-08-30 — — WO claimed
US-7811711-B2 Formed by fusion with carbon fibers, gelation, supercritical solvent extraction, and pyrolysis; for electrolytic fuel cells and batteries Lawrennce Livermore National Security, LLC (US) 2010-10-12 — — US claimed
US-20090017339-A1 Formed by fusion with carbon fibers, gelation, supercritical solvent extraction, and pyrolysis; for electrolytic fuel cells and batteries LAWRENCE LIVERMORE NATIONAL SECURITY, LLC 2009-01-15 — — US claimed
US-7410718-B2 Formed by fusion with carbon fibers, gelation, supercritical solvent extraction, and pyrolysis; for electrolytic fuel cells and batteries LAWRENCE LIVERMORE NATIONAL SECURITY, LLC (US) 2008-08-12 — — US claimed
US-20060282914-A1 Targeted dna insertion in plants BASF AGRICULTURAL SOLUTIONS US LLC 2006-12-14 — — US claimed
EP-0891182-B1 ENZYME ASSISTED DYEING OF KERATINOUS FIBRES NOVOZYMES AS (DK) 2001-11-14 — — EP claimed
EP-0863950-B1 HAIR DYEING COMPOSITION NOVOZYMES AS (DK) 2001-10-10 — — EP claimed
EP-0865465-B1 LACCASES WITH IMPROVED DYEING PROPERTIES NOVOZYMES AS (DK) 2001-05-30 — — EP claimed
US-5948121-A PERMANENT DYEING OF KERATINOUS FIBERS. LACCASE DERIVED FROM A STRAIN OF THE GENUS MYCELIOPHTHORA NOVO NORDISK A/S (DK) 1999-09-07 — — US claimed
EP-0865465-A1 LACCASES WITH IMPROVED DYEING PROPERTIES NOVO NORDISK A/S (DK) 1998-09-23 — — EP claimed
WO-1997019999-A1 LACCASES WITH IMPROVED DYEING PROPERTIES NOVO NORDISK A/S (DK) 1997-06-05 — — WO claimed
EP-0683428-A1 Thermal transfer imaging system based on the heat transfer of a reducing agent for reducing a silver source to metallic silver AGFA-GEVAERT N.V. (BE) 1995-11-22 — — EP claimed
CN-114657215-A Method and device for producing butanol by co-culture fermentation of aerobic bacteria and anaerobic bacteria 中国石油化工股份有限公司 2022-06-24 — — CN disclosed
CN-110505874-A Molecule and relative intermediate, composition and method with desinsection effectiveness DOW AGROSCIENCES LLC 2019-11-26 — — CN disclosed
CN-106572658-B Molecule and relative intermediate, composition and method with certain disinsection efficiencies 美国陶氏益农公司 2019-11-08 — — CN disclosed
CN-110087469-A Molecule and relative intermediate, composition and method with certain desinsection effectiveness 美国陶氏益农公司 2019-08-02 — — CN disclosed
US-4381973-A RECTIFICATION OF PRODUCT BAYER AKTIENGESELLSCHAFT (DE) 1983-05-03 — — US disclosed
US-4182917-A Process for the preparation of polyhydric phenols BAYER AKTIENGESELLSCHAFT (DE) 1980-01-08 — — US disclosed
US-4047953-A PHOTOGRAPHIC FILMS EASTMAN KODAK COMPANY (US) 1977-09-13 — — US disclosed
US-3968174-A MULTISTAGE HALCON INTERNATIONAL, INC. (US) 1976-07-06 — — US disclosed
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