SCHEMBL5370047

SCHEMBL5370047

CC(=O)OC/C=C(\C)C(=O)O

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 5/20 0.48
ALOX15 P16050 2/20 0.48
LMNA P02545 1/20 0.40
HSD17B10 Q99714 1/20 0.40
PTPN1 P18031 1/20 0.40
CHRM5 P08912 2/20 0.33
CHRM1 P11229 2/20 0.33
CHRM3 P20309 2/20 0.33
PGR P06401 1/20 0.33
CHRM2 P08172 1/20 0.33
CHRM4 P08173 1/20 0.33
HTR1A P08908 1/20 0.33
CHRNB2 P17787 1/20 0.33
TBXA2R P21731 1/20 0.33
CHRNB4 P30926 1/20 0.33
CHRNA3 P32297 1/20 0.33
CHRNA7 P36544 1/20 0.33
CHRNA4 P43681 1/20 0.33
SMN1; SMN2 Q16637 1/20 0.33
CHRNA10 Q9GZZ6 1/20 0.33

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
SCHEMBL5370053 1.00 ALDH1A1 (0.48) ALDH1A1ALOX15LMNAHSD17B10PTPN1
SCHEMBL14906813 1.00 ALDH1A1 (0.48) ALDH1A1ALOX15LMNAHSD17B10PTPN1
SCHEMBL1073337 0.82 ALDH1A1 (0.71) ALDH1A1ALOX15PTPN1
SCHEMBL1073336 0.82 ALDH1A1 (0.71) ALDH1A1ALOX15PTPN1
SCHEMBL6250744 0.82 ALOX15 (0.41) ALDH1A1ALOX15LMNAHSD17B10CHRM5
Hydrogen Peroxide SCHEMBL31395241 0.80 ALDH1A1 (0.63) ALDH1A1ALOX15LMNAHSD17B10PTPN1
SCHEMBL14334247 0.79 ALDH1A1 (0.47) ALDH1A1ALOX15LMNAHSD17B10PTPN1
SCHEMBL14334248 0.79 ALDH1A1 (0.47) ALDH1A1ALOX15LMNAHSD17B10PTPN1
SCHEMBL7772775 0.79 ALDH1A1 (0.47) ALDH1A1ALOX15LMNAHSD17B10PTPN1
SCHEMBL1617620 0.79 MGAM (0.43) ALDH1A1ALOX15GAA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116005179-B Method for preparing FCAA by electrochemical in-situ oxidation of FCA 万华化学集团股份有限公司 2025-04-01 CN claimed
CN-116288433-A Method for preparing FCAA by cathode-anode synergistic electrochemical oxidation of FCA 万华化学集团股份有限公司 2023-06-23 CN claimed
CN-116005179-A Method for preparing FCAA by electrochemical in-situ oxidation of FCA 万华化学集团股份有限公司 2023-04-25 CN claimed
CN-116005179-B Method for preparing FCAA by electrochemical in-situ oxidation of FCA 万华化学集团股份有限公司 2025-04-01 CN disclosed
CN-116288433-A Method for preparing FCAA by cathode-anode synergistic electrochemical oxidation of FCA 万华化学集团股份有限公司 2023-06-23 CN disclosed
CN-116005179-A Method for preparing FCAA by electrochemical in-situ oxidation of FCA 万华化学集团股份有限公司 2023-04-25 CN disclosed
EP-2723713-B1 METHOD FOR MAKING NEW INTERMEDIATES FOR THE VITAMIN A AND -CAROTENE SYNTHESIS DSM IP ASSETS BV (NL) 2018-04-11 EP disclosed
EP-2723713-B1 METHOD FOR MAKING NEW INTERMEDIATES FOR THE VITAMIN A AND -CAROTENE SYNTHESIS DSM IP ASSETS BV (NL) 2018-04-11 EP disclosed
EP-2723707-B1 NEW ACID CHLORIDE DSM IP ASSETS BV (NL) 2017-10-25 EP disclosed
EP-2723707-B1 NEW ACID CHLORIDE DSM IP ASSETS BV (NL) 2017-10-25 EP disclosed
US-9309194-B2 Intermediates for the vitamin A and β-carotene synthesis DSM IP ASSETS B.V. (NL) 2016-04-12 US disclosed
WO-2012175398-A1 NEW INTERMEDIATES FOR THE VITAMIN A AND β-CAROTENE SYNTHESIS DSM IP ASSETS B.V. (NL) 2012-12-27 WO disclosed
WO-2012175395-A1 NEW ACID CHLORIDE DSM IP ASSETS B.V. (NL) 2012-12-27 WO disclosed
WO-2012175398-A1 NEW INTERMEDIATES FOR THE VITAMIN A AND β-CAROTENE SYNTHESIS DSM IP ASSETS B.V. (NL) 2012-12-27 WO disclosed
US-7276622-B2 Method for producing oxygen-containing compound SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2007-10-02 US disclosed
US-20060173221-A1 Method for producing oxygen-containing compound SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2006-08-03 US disclosed
EP-1609777-A1 METHOD FOR PRODUCING OXYGEN-CONTAINING COMPOUND Sumitomo Chemical Company, Limited (JP) 2005-12-28 EP disclosed
EP-0673911-B1 Process for producing optically active carboxylic acids and chiral ligands for this purpose TAKASAGO PERFUMERY CO LTD (JP) 1999-01-20 EP disclosed
US-5563295-A HYDROGENATION OF OLEFINIC CARBOXYLIC ACID USING RUTHENIUM-PHOSPHINE COMPLEX CATALYST TAKASAGO INTERNATIONAL CORPORATION (JP) 1996-10-08 US disclosed
EP-0673911-A1 Process for producing optically active carboxylic acids and chiral ligands for this purpose Takasago International Corporation (JP) 1995-09-27 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-20060173221-A1 Method for producing oxygen-containing compound GPX4, DUOX2, SCO2 ALDH1A1 863/4885ALOX15 76/4885LMNA 4036/4885

“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.