SCHEMBL2806074

SCHEMBL2806074

O=C(O)NCc1cccc(O)c1

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 2/20 0.59
CYP2D6 P10635 1/20 0.59
CYP2C9 P11712 1/20 0.59
TSHR P16473 1/20 0.59
CYP2C19 P33261 1/20 0.59
PKM P14618 2/20 0.58
CYP3A4 P08684 1/20 0.58
ALOX15 P16050 1/20 0.58
NFKB1 P19838 1/20 0.58
MAPK1 P28482 1/20 0.58
LMNA P02545 2/20 0.56
MAPT P10636 2/20 0.56
KMT2A Q03164 1/20 0.56
KDM4E B2RXH2 1/20 0.56
BLM P54132 1/20 0.56
PMP22 Q01453 1/20 0.56
HIF1A Q16665 1/20 0.54
ROCK2 O75116 1/20 0.54
ROCK1 Q13464 1/20 0.54
MMP1 P03956 1/20 0.53

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
SCHEMBL2450156 0.90 AOC3 (0.56) CYP1A2CYP2D6CYP2C9TSHRCYP2C19
SCHEMBL8059189 0.88 CYP1A2 (0.68) CYP1A2CYP2D6CYP2C9TSHRCYP2C19
SCHEMBL7017296 0.84 BRD4 (0.50) CYP1A2CYP2D6CYP2C9TSHRCYP2C19
SCHEMBL5725833 0.83 CYP1A2 (0.56) CYP1A2PKMCYP3A4ALOX15NFKB1
SCHEMBL358332 0.83 CYP1A2 (0.61) CYP1A2CYP2C9CYP2C19PKMCYP3A4
SCHEMBL18722706 0.83 CYP1A2 (0.56) CYP1A2PKMCYP3A4ALOX15NFKB1
SCHEMBL31724652 0.83 CYP1A2 (0.56) CYP1A2PKMCYP3A4ALOX15NFKB1
SCHEMBL5724150 0.82 ROCK2 (0.68) ROCK2ROCK1SRCALDH1A1
SCHEMBL2749289 0.81 SPR (0.63) KMT2AMMP1MMP2MMP9ALDH1A1
SCHEMBL2567513 0.81 HSD17B1 (0.55) CYP1A2CYP2D6CYP2C9TSHRCYP2C19

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2024006742-A2 NRF2 PROTEIN DEGRADERS DRACEN PHARMACEUTICALS, INC. (US) 2024-01-04 WO disclosed
WO-2023213728-A1 SUBSTITUTED ARYL ESTERS OF COUMARIN-3-CARBOXYLIC ACID AND THEIR USE AS HOST CELL PROTEASES INHIBITORS Université de Liège (BE) 2023-11-09 WO disclosed
US-20230310445-A1 LOX ENZYME INHIBITING METHODS AND COMPOSITIONS ANOVIA BIOSCIENCES, INC. 2023-10-05 US disclosed
EP-4138824-A1 LOX ENZYME INHIBITING METHODS AND COMPOSITIONS Anovia Biosciences, Inc. (US) 2023-03-01 EP disclosed
US-20210353683-A1 ADDITIVE FOR MEDIUM FOR PROMOTING PRODUCTION OF PARACRINE FACTOR NISSAN CHEMICAL CORPORATION (JP) 2021-11-18 US disclosed
WO-2021216592-A1 LOX ENZYME INHIBITING METHODS AND COMPOSITIONS ANOVIA BIOSCIENCES, INC. (US) 2021-10-28 WO disclosed
EP-3851519-A1 ADDITIVE FOR MEDIUM FOR PROMOTING PRODUCTION OF PARACRINE FACTOR Nissan Chemical Corporation (JP) 2021-07-21 EP disclosed
WO-2020158840-A1 ANTI-CANCER AGENT 日産化学株式会社 2020-08-06 WO disclosed
US-10626112-B2 Heterocyclic sulfonamide derivative and medicine comprising same EA PHARMA CO., LTD. (JP) 2020-04-21 US disclosed
EP-3101015-B1 HETEROCYCLIC SULFONAMIDE DERIVATIVE AND MEDICINE COMPRISING SAME EA PHARMA CO LTD (JP) 2019-09-18 EP disclosed
CN-101479267-B Purine derivatives as A2A agonists NOVARTIS AG 2012-05-02 CN disclosed
US-20100240671-A1 SUBSTITUTED HETEROCYCLIC COMPOUNDS INCYTE CORPORATION (US) 2010-09-23 US disclosed
WO-2010108059-A1 SUBSTITUTED PYRIMIDINE DERIVATIVES AS ANTAGONISTS OF THE HISTAMINE H4 RECEPTOR INCYTE CORPORATION (US) 2010-09-23 WO disclosed
CN-101479267-A Purine derivatives as A2A agonists NOVARTIS AG (CH) 2009-07-08 CN disclosed
CN-101472925-A As adenosine A2APurine derivatives of receptor agonists NOVARTIS AG (CH) 2009-07-01 CN disclosed
US-7365085-B2 Compounds and methods SMITHKLINE BEECHAM CORPORATION (US) 2008-04-29 US disclosed
EP-1575495-A2 COMPOUNDS AND METHODS SmithKline Beecham Corporation (US) 2005-09-21 EP disclosed
US-20050113580-A1 Amide compounds and methods of using the same SMITHKLINE BEECHAM CORP 2005-05-26 US disclosed
WO-2003082205-A2 COMPOUNDS AND METHODS SMITHKLINE BEECHAM CORPORATION (US) 2003-10-09 WO disclosed
US-4131751-A PHENYLENE, PLANT GROWTH REGULATORS BASF AKTIENGESELLSCHAFT (DE) 1978-12-26 US 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 (5 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-20230310445-A1 LOX ENZYME INHIBITING METHODS AND COMPOSITIONS LOX, LOXL1, LOXL2 CYP1A2 423/4885CYP2D6 710/4885CYP2C9 612/4885
US-20100240671-A1 SUBSTITUTED HETEROCYCLIC COMPOUNDS HRH4, HRH2, HRH1 CYP1A2 479/4885CYP2D6 263/4885CYP2C9 190/4885
US-20210353683-A1 ADDITIVE FOR MEDIUM FOR PROMOTING PRODUCTION OF PARACRINE FACTOR HGF, HDGF, FGF2 CYP1A2 4831/4885CYP2D6 4876/4885CYP2C9 4885/4885
US-20050113580-A1 Amide compounds and methods of using the same NR1H2, NR1H3, PPARA CYP1A2 301/4885CYP2D6 503/4885CYP2C9 366/4885
US-10626112-B2 Heterocyclic sulfonamide derivative and medicine comprising same TRPA1, TRPV1, TRPV2 CYP1A2 758/4885CYP2D6 774/4885CYP2C9 820/4885

“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.