Catechol

Catechol

SCHEMBL1143838

O=S(=O)(O)O.O=S(=O)(O)O.Oc1ccccc1O

nearest known ligand 0.67

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

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

The experimentally established mechanism targets of Catechol. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ MAOA known ✓ P21397 2/20 0.42
▸ KDM4E B2RXH2 5/20 0.67
▸ ALDH1A1 P00352 5/20 0.67
▸ CA2 P00918 5/20 0.67
▸ SMN1; SMN2 Q16637 4/20 0.67
▸ HPGD P15428 4/20 0.67
▸ CA4 P22748 4/20 0.67
▸ MAPT P10636 4/20 0.67
▸ ALOX15 P16050 3/20 0.67
▸ CA12 O43570 3/20 0.67
▸ CA14 Q9ULX7 3/20 0.67
▸ HSD17B10 Q99714 3/20 0.67
▸ LMNA P02545 3/20 0.67
▸ EGFR P00533 2/20 0.67
▸ FYN P06241 2/20 0.67
▸ MMP9 P14780 2/20 0.67
▸ RECQL P46063 2/20 0.67
▸ TDP1 Q9NUW8 2/20 0.67
▸ NPC1 O15118 2/20 0.67
▸ CA3 P07451 2/20 0.67

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 SCHEMBL29652083 1.00 KDM4E (0.67) KDM4EALDH1A1CA2SMN1; SMN2HPGD
Catechol SCHEMBL235068 1.00 KDM4E (0.67) KDM4EALDH1A1CA2SMN1; SMN2HPGD
Catechol SCHEMBL27989011 1.00 KDM4E (0.67) KDM4EALDH1A1CA2SMN1; SMN2HPGD
Catechol SCHEMBL23111816 0.97 ALDH1A1 (0.62) KDM4EALDH1A1CA2SMN1; SMN2HPGD
Catechol SCHEMBL11405646 0.97 ALDH1A1 (0.62) KDM4EALDH1A1CA2SMN1; SMN2HPGD
Catechol SCHEMBL11778548 0.88 SMN1; SMN2 (0.59) KDM4EALDH1A1CA2SMN1; SMN2HPGD
Catechol SCHEMBL10535949 0.84 KDM4E (0.48) KDM4EALDH1A1CA2SMN1; SMN2HPGD
Catechol SCHEMBL1491270 0.84 ALDH1A1 (0.62) KDM4EALDH1A1CA2SMN1; SMN2HPGD
Catechol SCHEMBL1143840 0.83 CA2 (0.53) KDM4EALDH1A1CA2SMN1; SMN2HPGD
Trifluoromethanesulfonic Acid SCHEMBL1712877 0.83 CA2 (0.53) KDM4EALDH1A1CA2SMN1; SMN2HPGD

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 6 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8367596-B2 Laundry detergent compositions in the form of an article THE PROCTER & GAMBLE COMPANY (US) 2013-02-05 — — US disclosed
US-20110028374-A1 LAUNDRY DETERGENT COMPOSITIONS IN THE FORM OF AN ARTICLE THE PROCTER & GAMBLE COMPANY 2011-02-03 — — US disclosed
US-5880258-A HIGHER ANTI-THROMBIN ACTIVITY BY SULFATING THE HYDROXYL GROUP OF TYROSINE RESIDUES; MUTANT AMINO ACID SEQUENCE ALLOWS MORE EFFICIENT ENZYME SULFATION JAPAN ENERGY CORPORATION (JP) 1999-03-09 — — US disclosed
US-5767235-A SULFATED TYOSINE NIPPON MINING COMPANY LIMITED (JP) 1998-06-16 — — US disclosed
EP-0531537-B1 HIRUDIN ANALOGUE OR SALT THEREOF, PRODUCTION THEREOF, AND ANTICOAGULANT CONTAINING THE SAME AS ACTIVE INGREDIENT JAPAN ENERGY CORP (JP) 1996-09-11 — — EP disclosed
EP-0531537-A1 HIRUDIN ANALOGUE OR SALT THEREOF, PRODUCTION THEREOF, AND ANTICOAGULANT CONTAINING THE SAME AS ACTIVE INGREDIENT JAPAN ENERGY CORPORATION (JP) 1993-03-17 — — EP disclosed
Send feedback