SCHEMBL1818192

SCHEMBL1818192

COC(=O)C(C)c1cccc(O)c1

nearest known ligand 0.62

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PTGS1 P23219 2/20 0.62
PTGS2 P35354 1/20 0.62
MT-CO2 P00403 1/20 0.50
ADRB1 P08588 2/20 0.47
ADRA1A P35348 2/20 0.47
MIF P14174 1/20 0.47
HTR2A P28223 1/20 0.47
HTR2B P41595 1/20 0.47
KMT2A Q03164 1/20 0.47
HIF1A Q16665 4/20 0.46
LMNA P02545 3/20 0.46
KDM4E B2RXH2 2/20 0.46
ADRB2 P07550 1/20 0.45
HTR1A P08908 1/20 0.45
ADRA2A P08913 1/20 0.45
ADRB3 P13945 1/20 0.45
TSHR P16473 1/20 0.45
ADRA2B P18089 1/20 0.45
ADRA2C P18825 1/20 0.45
NFKB1 P19838 1/20 0.45

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
SCHEMBL7806911 1.00 PTGS1 (0.62) PTGS1PTGS2MT-CO2ADRB1ADRA1A
SCHEMBL7807735 0.84 KMT2A (0.55) PTGS1PTGS2ADRB1ADRA1AMIF
SCHEMBL31074078 0.83 ADRB1 (0.45) PTGS1PTGS2ADRB1ADRA1AMIF
SCHEMBL24260675 0.83 ADRB1 (0.45) PTGS1PTGS2ADRB1ADRA1AMIF
SCHEMBL3905021 0.83 ADRB1 (0.45) PTGS1PTGS2ADRB1ADRA1AMIF
SCHEMBL5285160 0.82 HIF1A (0.49) PTGS1PTGS2ADRB1ADRA1AMIF
SCHEMBL5285167 0.82 HIF1A (0.49) PTGS1PTGS2ADRB1ADRA1AMIF
SCHEMBL1653533 0.82 PTGS1 (0.62) PTGS1PTGS2MT-CO2KMT2AHPGD
SCHEMBL29484096 0.82 PTGS1 (0.62) PTGS1PTGS2MT-CO2KMT2AHPGD
SCHEMBL1492817 0.82 PTGS1 (0.62) PTGS1PTGS2MT-CO2KMT2AHPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117142955-A Method for catalyzing carbonylation esterification reaction by cobalt promoted by molybdenum disulfide 中国科学院兰州化学物理研究所 2023-12-01 CN claimed
CN-116730836-A Method for catalyzing carbonylation esterification reaction by cobalt salt activated by synthesis gas 中国科学院兰州化学物理研究所 2023-09-12 CN claimed
CN-117142955-A Method for catalyzing carbonylation esterification reaction by cobalt promoted by molybdenum disulfide 中国科学院兰州化学物理研究所 2023-12-01 CN disclosed
CN-116730836-A Method for catalyzing carbonylation esterification reaction by cobalt salt activated by synthesis gas 中国科学院兰州化学物理研究所 2023-09-12 CN disclosed
CN-110092709-B Synthetic method of non-urethane intermediate 2-phenyl-1, 3-propylene glycol 深圳市第二人民医院 2022-03-04 CN disclosed
US-20120316169-A1 2-ARYL-PROPIONAMIDE DERIVATIVES USEFUL AS BRADYKININ RECEPTOR ANTAGONISTS AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM Dompé S.p.A. (IT) 2012-12-13 US disclosed
EP-2493846-A1 2-ARYL-PROPIONAMIDE DERIVATIVES USEFUL AS BRADYKININ RECEPTOR ANTAGONISTS AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM Dompe S.p.A. (IT) 2012-09-05 EP disclosed
CN-102656140-A 2-aryl-propionamide derivatives useful as bradykinin receptor antagonists and pharmaceutical compositions containing them DOMPE SPA 2012-09-05 CN disclosed
WO-2011051375-A1 2-ARYL-PROPIONAMIDE DERIVATIVES USEFUL AS BRADYKININ RECEPTOR ANTAGONISTS AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM Dompé S.p.A. (IT) 2011-05-05 WO disclosed
EP-2316820-A1 2-aryl-propionamide derivatives useful as bradykinin receptor antagonists and pharmaceutical compositions containing them Dompe S.p.A. (IT) 2011-05-04 EP disclosed
WO-2010138901-A1 CARBOXYLIC ACID-CONTAINING COMPOUNDS, DERIVATIVES THEREOF, AND RELATED METHODS OF USE BIOGEN IDEC MA INC (US) 2010-12-02 WO disclosed
EP-1602642-A1 IMINO ETHER DERIVATIVE COMPOUNDS AND DRUGS CONTAINING THE COMPOUNDS AS THE ACTIVE INGREDIENT ONO PHARMACEUTICAL CO., LTD. (JP) 2005-12-07 EP disclosed
EP-1585733-A1 HETEROCYCLIC PPAR MODULATORS ELI LILLY AND COMPANY (US) 2005-10-19 EP disclosed
EP-1453795-A2 ESTERS AND AMIDES AS PPAR-ALPHA AGONISTS Dr. Reddy's Laboratories Ltd. (IN) 2004-09-08 EP disclosed
WO-2004063166-A1 HETEROCYCLIC PPAR MODULATORS ELI LILLY AND COMPANY (US) 2004-07-29 WO disclosed
US-20030229083-A1 Compounds and their use in medicine, process for their preparation and pharmaceutical compositions containing them DR. REDDY'S LABORATORIES LIMITED 2003-12-11 US disclosed
WO-2003048116-A2 ESTERS AND AMIDES AS PPAR-ALPHA AGONISTS ____________ DR. REDDY'S LABORATORIES LTD. (IN) 2003-06-12 WO disclosed
US-4761420-A CARDIOVASCULAR DISORDERS LABORATOIRES SYNTEX S.A. (FR) 1988-08-02 US disclosed
EP-0249245-A2 Antihypertensive dihydropyridine derivatives LABORATOIRES SYNTEX S.A. (FR) 1987-12-16 EP disclosed
US-4117234-A DERIVATIVES OF 2-(6-PHENYLHEX-3-ENYL)-CYCLOPENT-2-EN-1-OL THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY (US) 1978-09-26 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 (2 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-20120316169-A1 2-ARYL-PROPIONAMIDE DERIVATIVES USEFUL AS BRADYKININ RECEPTOR ANTAGONISTS AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM BDKRB2, BDKRB1, CNR2 PTGS1 79/4885PTGS2 66/4885MT-CO2 4144/4885
US-20030229083-A1 Compounds and their use in medicine, process for their preparation and pharmaceutical compositions containing them GPR119, LIPA, PCSK9 PTGS1 2630/4885PTGS2 3694/4885MT-CO2 2583/4885

“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.