SCHEMBL712291

SCHEMBL712291

CO/C=C(/C(=O)OC)c1ccccc1OCc1ccccc1

nearest known ligand 0.59

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
SGMS2 Q8NHU3 5/20 0.57
NPC1 O15118 1/20 0.51
LMNA P02545 1/20 0.51
MAPT P10636 1/20 0.51
L3MBTL1 Q9Y468 1/20 0.51
GAA P10253 1/20 0.50
MEN1 O00255 2/20 0.48
KMT2A Q03164 2/20 0.48
ALDH1A1 P00352 1/20 0.48
HTT P42858 1/20 0.48
BRD4 O60885 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
SCHEMBL7164705 1.00 SGMS2 (0.57) SGMS2NPC1LMNAMAPTL3MBTL1
SCHEMBL1097807 1.00 SGMS2 (0.57) SGMS2NPC1LMNAMAPTL3MBTL1
SCHEMBL9642440 0.89 SGMS2 (0.59) SGMS2NPC1LMNAMAPTL3MBTL1
SCHEMBL1097809 0.89 SGMS2 (0.59) SGMS2NPC1LMNAMAPTL3MBTL1
SCHEMBL10442994 0.89 SGMS2 (0.52) SGMS2NPC1LMNAMAPTL3MBTL1
SCHEMBL5046789 0.89 SGMS2 (0.52) SGMS2NPC1LMNAMAPTL3MBTL1
SCHEMBL5046787 0.89 SGMS2 (0.52) SGMS2NPC1LMNAMAPTL3MBTL1
SCHEMBL9647587 0.88 SGMS2 (0.47) SGMS2NPC1LMNAMAPTL3MBTL1
SCHEMBL9730334 0.88 SGMS2 (0.47) SGMS2NPC1LMNAMAPTL3MBTL1
SCHEMBL10443318 0.88 SGMS2 (0.58) SGMS2NPC1LMNAMAPTL3MBTL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2308825-B1 Process for the preparation of an intermediate for azoxystrobin SYNGENTA LTD (GB) 2014-05-21 EP disclosed
EP-1891020-B1 PROCESSES FOR THE PREPARATION OF AZOXYSTROBIN USING DABCO AS A CATALYST AND NOVEL INTERMEDIATES USED IN THE PROCESSES SYNGENTA LTD (GB) 2013-06-05 EP disclosed
US-8124761-B2 Coupling of methyl (E)-2-{2-[6-chloropyrimidin-4-yloxy]phenyl}-3-methoxyacrylate with 2-cyanophenyl in DMF with 2 mol % DABCO; significantly smaller amounts of this relatively expensive catalyst may be used without compromising the yield SYNGENTA LIMITED (GB) 2012-02-28 US disclosed
US-8124761-B2 Coupling of methyl (E)-2-{2-[6-chloropyrimidin-4-yloxy]phenyl}-3-methoxyacrylate with 2-cyanophenyl in DMF with 2 mol % DABCO; significantly smaller amounts of this relatively expensive catalyst may be used without compromising the yield SYNGENTA LIMITED (GB) 2012-02-28 US disclosed
US-8124761-B2 Coupling of methyl (E)-2-{2-[6-chloropyrimidin-4-yloxy]phenyl}-3-methoxyacrylate with 2-cyanophenyl in DMF with 2 mol % DABCO; significantly smaller amounts of this relatively expensive catalyst may be used without compromising the yield SYNGENTA LIMITED (GB) 2012-02-28 US disclosed
EP-2308825-A1 Process for the preparation of an intermediate for azoxystrobin Syngenta Limited (GB) 2011-04-13 EP disclosed
EP-2308825-A1 Process for the preparation of an intermediate for azoxystrobin Syngenta Limited (GB) 2011-04-13 EP disclosed
US-20080214587-A1 Processes For the Preparation of Azoxystrobin Using Dabco as a Catalyst and Novel Intermediates Used in the Processes SYNGENTA CROP PROTECTION, INC. (US) 2008-09-04 US disclosed
US-20080214587-A1 Processes For the Preparation of Azoxystrobin Using Dabco as a Catalyst and Novel Intermediates Used in the Processes SYNGENTA CROP PROTECTION, INC. (US) 2008-09-04 US disclosed
EP-0178826-B2 Fungicides SYNGENTA LTD (GB) 2003-04-09 EP disclosed
US-5602076-A INSECTICIDES, NEMATOCIDES ZENECA LIMITED (GB) 1997-02-11 US disclosed
US-5470819-A Plant growth regulators, insecticides ZENECA LIMITED (GB) 1995-11-28 US disclosed
EP-0260794-B1 Substituted phenyl-2-propenoic acid derivatives and their use as fungicides ZENECA LTD (GB) 1994-06-22 EP disclosed
EP-0256667-B1 SUBSTITUTED PHENYL-2-PROPENOIC ACID DERIVATIVES USEFUL IN AGRICULTURE IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1992-12-30 EP disclosed
US-5120755-A FUNGICIDAL SUBSTITUTED ACRYLIC ACID ESTERS BAYER AKTIENGESELLSCHAFT (DE) 1992-06-09 US disclosed
EP-0178826-B1 FUNGICIDES ZENECA LIMITED (GB) 1991-12-18 EP disclosed
US-5057146-A CERTAIN 2-PYRIDYL OXY-PHENYL ACRYLATES HAVING FUNGICIDAL, INSECTICIDAL, NEMATOCIDAL AND PLANT GROWTH REGULATING ACTIVITY IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1991-10-15 US disclosed
EP-0391451-A1 Fungicides IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1990-10-10 EP disclosed
EP-0387923-A2 Fungicides ZENECA LIMITED (GB) 1990-09-19 EP disclosed
EP-0242081-A1 Fungicides ZENECA LIMITED (GB) 1987-10-21 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-20080214587-A1 Processes For the Preparation of Azoxystrobin Using Dabco as a Catalyst and Novel Intermediates Used in the Processes DDT, AOC3, DAO SGMS2 4000/4885NPC1 4635/4885LMNA 3353/4885

“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.