SCHEMBL6903471

SCHEMBL6903471

CCCCCCC(C)=C=O

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CES2 O00748 4/20 0.50
CES1 P23141 4/20 0.50
GPR84 Q9NQS5 7/20 0.48
PPARG P37231 7/20 0.48
PPARD Q03181 7/20 0.48
PPARA Q07869 7/20 0.48
HDAC11 Q96DB2 5/20 0.48
TSHR P16473 5/20 0.48
PTPN1 P18031 3/20 0.48
ALDH1A1 P00352 3/20 0.48
TLR2 O60603 2/20 0.48
TDP1 Q9NUW8 2/20 0.48
FABP4 P15090 2/20 0.48
SLC22A6 Q4U2R8 1/20 0.48
SLC22A8 Q8TCC7 1/20 0.48
MEN1 O00255 1/20 0.48
ESR1 P03372 1/20 0.48
ALOX15 P16050 1/20 0.48
PDE4A P27815 1/20 0.48
KMT2A Q03164 1/20 0.48

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
SCHEMBL29083518 1.00 CES2 (0.50) CES2CES1GPR84PPARGPPARD
SCHEMBL6903742 1.00 CES2 (0.50) CES2CES1GPR84PPARGPPARD
SCHEMBL6904919 1.00 CES2 (0.50) CES2CES1GPR84PPARGPPARD
SCHEMBL2513328 0.97
SCHEMBL6898683 0.90
SCHEMBL5828221 0.78
SCHEMBL28237361 0.78 TSHR (0.57) GPR84PPARGPPARDPPARAHDAC11
SCHEMBL20474524 0.78 TSHR (0.57) GPR84PPARGPPARDPPARAHDAC11
SCHEMBL7181805 0.77 CES2 (0.46) CES2CES1GPR84PPARGPPARD
SCHEMBL3648861 0.77 CES2 (0.46) CES2CES1GPR84PPARGPPARD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116669572-A Heat treated soy flour 皆食得公司 2023-08-29 CN claimed
CN-115052932-A Composition, method for preparing copolymer and end use of copolymer 美国陶氏有机硅公司 2022-09-13 CN disclosed
CN-113348199-A Branched organosilicon compounds, methods of making branched organosilicon compounds, and copolymers formed therewith 美国陶氏有机硅公司 2021-09-03 CN disclosed
CN-113330055-A Acrylate-functional branched organosilicon compounds, methods of making, and copolymers formed therewith 美国陶氏有机硅公司 2021-08-31 CN disclosed
CN-113330054-A Branched organosilicon compounds, methods of making, and copolymers formed therewith 美国陶氏有机硅公司 2021-08-31 CN disclosed
CN-113195596-A Branched organosilicon compounds, method for producing branched organosilicon compounds, and compositions containing branched organosilicon compounds 美国陶氏有机硅公司 2021-07-30 CN disclosed
CN-113166423-A Branched organosilicon compounds, method for producing branched organosilicon compounds, and compositions containing branched organosilicon compounds 美国陶氏有机硅公司 2021-07-23 CN disclosed
EP-1122235-B1 Process for preparing 1,3-alkanediol from epoxide derivative DAVY PROCESS TECHN LTD (GB) 2004-09-15 EP disclosed
US-6600065-B2 Process for preparing 3-hydroxyesters from epoxide derivatives DAVY PROCESS TECHNOLOGY LTD. (GB) 2003-07-29 US disclosed
US-20030109744-A1 PROCESS FOR PREPARING 3-HYDROXYESTERS FROM EPOXIDE DERIVATIVES DAVY PROCESS TECHNOLOGY LTD. (GB) 2003-06-12 US disclosed
EP-1304321-A2 Process for preparing 3-Hydroxyesters from epoxide derivatives SAMSUNG ELECTRONICS CO., LTD. (KR) 2003-04-23 EP disclosed
US-6541414-B2 For preparing an 1,3-alkanediol through carbonylation of an epoxide derivative SAMSUNG ELECTRONICS CO., LTD. (KR) 2003-04-01 US disclosed
US-6521801-B2 Catalytic carbonylation of epoxide derivative includes reacting with alcohol and carbon monoxide to form hydroxyester which is hydrogenated to form diol SAMSUNG ELECTRONICS CO., LTD. (KR) 2003-02-18 US disclosed
US-6465680-B2 USING COBALT CATALYST AND PROMOTER SAMSUNG ELECTRONICS CO., LTD. (KR) 2002-10-15 US disclosed
US-20020099245-A1 For preparing an 1,3-alkanediol through carbonylation of an epoxide derivative SAMSUNG ELECTRONICS CO., LTD (KR) 2002-07-25 US disclosed
US-20020065439-A1 Catalytic carbonylation of epoxide derivative includes reacting with alcohol and carbon monoxide to form hydroxyester which is hydrogenated to form diol DAVY PROCESS TECHNOLOGY LIMITED (GB) 2002-05-30 US disclosed
US-20020035290-A1 Process for preparing malonate derivatives or beta -keto esters from epoxide derivatives SAMSUNG ELECTRONICS CO., LTD. 2002-03-21 US disclosed
US-6348632-B1 Process for preparing 1,3-alkanediol from epoxide derivative SAMSUNG ELECTRONICS CO. LTD. (KR) 2002-02-19 US disclosed
EP-1122235-A2 Process for preparing 1,3-alkanediol from epoxide derivative SAMSUNG ELECTRONICS CO., LTD. (KR) 2001-08-08 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 (4 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-20020099245-A1 For preparing an 1,3-alkanediol through carbonylation of an epoxide derivative CYP2E1, ADH1C, OR51E2 CES2 173/4885CES1 235/4885GPR84 4824/4885
US-20020035290-A1 Process for preparing malonate derivatives or beta -keto esters from epoxide derivatives CYP4A11, ME1, CYP2E1 CES2 411/4885CES1 157/4885GPR84 3866/4885
US-20030109744-A1 PROCESS FOR PREPARING 3-HYDROXYESTERS FROM EPOXIDE DERIVATIVES CYP2E1, HMOX2, CYP4A11 CES2 250/4885CES1 173/4885GPR84 3376/4885
US-20020065439-A1 Catalytic carbonylation of epoxide derivative includes reacting with alcohol and carbon monoxide to form hydroxyester which is hydrogenated to form diol CYP2E1, ADH1C, ADH1A CES2 99/4885CES1 151/4885GPR84 4439/4885

“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.