Catechol

Catechol

SCHEMBL2707627

CC(=O)O.Oc1ccccc1O

nearest known ligand 0.62

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Known targets — ChEMBL curated mechanism

ADRA2AADRA2BADRA2CADRB2AGTR1AVPR1AAVPR1BAVPR2BDKRB2CALCRCHRNA3CHRNB4ESR1ESR2GHSRGNRHRGSC1HSPA8MALT1MC1RMC4RNOS1NOS2NOS3OPRK1OXTRRAMP1RAMP2RAMP3SCN5ASSTR1SSTR2SSTR3SSTR4SSTR5dacAdacBdacCfolPftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

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
CA2 P00918 5/20 0.62
ALDH1A1 P00352 5/20 0.62
HPGD P15428 5/20 0.62
CA12 O43570 4/20 0.62
CA14 Q9ULX7 4/20 0.62
KDM4E B2RXH2 4/20 0.62
MAPT P10636 4/20 0.62
HSD17B10 Q99714 4/20 0.62
CA4 P22748 3/20 0.62
SMN1; SMN2 Q16637 3/20 0.62
LMNA P02545 3/20 0.62
NFKB1 P19838 2/20 0.62
NPC1 O15118 2/20 0.62
FYN P06241 2/20 0.62
GMNN O75496 1/20 0.62
EGFR P00533 1/20 0.62
POLB P06746 1/20 0.62
CA3 P07451 1/20 0.62
CYP3A4 P08684 1/20 0.62
MMP9 P14780 1/20 0.62

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 SCHEMBL8411371 1.00 CA2 (0.62) CA2ALDH1A1HPGDCA12CA14
Catechol SCHEMBL27477125 0.97 CA2 (0.59) CA2ALDH1A1HPGDCA12CA14
Catechol SCHEMBL28266919 0.92 CA2 (0.53) CA2ALDH1A1HPGDCA12CA14
Catechol SCHEMBL2555536 0.90 KDM4E (0.67) CA2ALDH1A1HPGDCA12CA14
Catechol SCHEMBL4622850 0.88 CA2 (0.56) CA2ALDH1A1HPGDCA12CA14
Catechol SCHEMBL10659163 0.88 KDM4E (0.62) CA2ALDH1A1HPGDCA12CA14
Catechol SCHEMBL27240704 0.87 MAPT (0.48) CA2ALDH1A1HPGDCA12CA14
Catechol SCHEMBL154583 0.87 ALDH1A1 (0.71) CA2ALDH1A1HPGDCA12CA14
Catechol SCHEMBL30530338 0.87 ALDH1A1 (0.71) CA2ALDH1A1HPGDCA12CA14
Catechol SCHEMBL21196902 0.87 ALDH1A1 (0.71) CA2ALDH1A1HPGDCA12CA14

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115895800-B Semi-water-based wafer substrate cleaning fluid composition and method of use 芯越微电子材料(嘉兴)有限公司 2024-12-27 CN claimed
CN-115895800-A Semi-aqueous wafer substrate cleaning solution composition and application method thereof 芯越微电子材料(嘉兴)有限公司 2023-04-04 CN claimed
US-20020045584-A1 Acyclic isoprenoid ether derivatives as chemotherapeutics WISCONSIN ALUMNI RESEARCH FOUNDATION 2002-04-18 US claimed
WO-2002005856-A2 ACYCLIC ISOPRENOID ETHER DERIVATIVES AS CHEMOTHERAPUETICS WISCONSIN ALUMNI RESEARCH FOUNDATION (US) 2002-01-24 WO claimed
CN-115895800-B Semi-water-based wafer substrate cleaning fluid composition and method of use 芯越微电子材料(嘉兴)有限公司 2024-12-27 CN disclosed
CN-117700565-A Recovery of component cellulose esters 伊士曼化工公司 2024-03-15 CN disclosed
CN-114072429-B Recovery of component cellulose esters 伊士曼化工公司 2023-12-26 CN disclosed
CN-115895800-A Semi-aqueous wafer substrate cleaning solution composition and application method thereof 芯越微电子材料(嘉兴)有限公司 2023-04-04 CN disclosed
CN-113813406-B Nano-particles for treating atherosclerosis by MRI and chemical excitation photodynamic therapy 南京鼓楼医院 2023-03-24 CN disclosed
CN-114681661-B Hemostatic powder and preparation method thereof 四川大学 2023-03-17 CN disclosed
CN-114072429-A Recovery of constituent cellulose ester 伊士曼化工公司 2022-02-18 CN disclosed
CN-113813406-A Nano-particles for treating atherosclerosis by MRI and chemical excitation photodynamic therapy 南京鼓楼医院 2021-12-21 CN disclosed
US-20030045461-A1 Composition and methods of esterified nitroxides gated with carboxylic acids SYNZYME TECHNOLOGIES, INC. 2003-03-06 US disclosed
US-20020045584-A1 Acyclic isoprenoid ether derivatives as chemotherapeutics WISCONSIN ALUMNI RESEARCH FOUNDATION 2002-04-18 US disclosed
WO-2002005856-A2 ACYCLIC ISOPRENOID ETHER DERIVATIVES AS CHEMOTHERAPUETICS WISCONSIN ALUMNI RESEARCH FOUNDATION (US) 2002-01-24 WO disclosed
US-5393776-A Tocotrienol analogs in the treatment of hypercholesterolemia and hyperlipidemia BRISTOL-MYERS SQUIBB COMPANY (US) 1995-02-28 US disclosed
EP-0571928-A1 Acyclic Tocotrienol analogs in the treatment of hypercholesterolemia and hyperlipidemia Bristol-Myers Squibb Company (US) 1993-12-01 EP disclosed
EP-0476493-A1 Acyclic tocotrienol analogs in the treatment of hypercholesterolemia and hyperlipidemia Bristol-Myers Squibb Company (US) 1992-03-25 EP disclosed
US-4740449-A Optical recording medium CANON KABUSHIKI KAISHA (JP) 1988-04-26 US disclosed
EP-0122523-A2 Diazotype compositions and materials Andrews Paper and Chemical Co., Inc. (US) 1984-10-24 EP disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20030045461-A1 Composition and methods of esterified nitroxides gated with carboxylic acids FPGS, NDUFAB1, ARG2 CA2 396/4885ALDH1A1 1001/4885HPGD 140/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.