SCHEMBL3987755

SCHEMBL3987755

CCOC(=O)C=C(C)NC(C(=O)O)c1ccc(O)cc1

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
FOLH1 Q04609 2/20 0.46
CA12 O43570 2/20 0.43
CA1 P00915 2/20 0.43
CA2 P00918 2/20 0.43
CA7 P43166 2/20 0.43
CA9 Q16790 2/20 0.43
CA14 Q9ULX7 2/20 0.43
NAALAD2 Q9Y3Q0 1/20 0.43
ATM Q13315 2/20 0.41
KMT2A Q03164 2/20 0.41
MAPT P10636 2/20 0.40
MDM4 O15151 1/20 0.40
LMNA P02545 1/20 0.40
MDM2 Q00987 1/20 0.40
YARS1 P54577 1/20 0.39
ESR2 Q92731 3/20 0.39
ESR1 P03372 2/20 0.39
MIF P14174 1/20 0.37
SMN1; SMN2 Q16637 1/20 0.35
SRC P12931 1/20 0.35

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
SCHEMBL3987754 1.00 FOLH1 (0.46) FOLH1CA12CA1CA2CA7
SCHEMBL9301284 0.89 MAPT (0.50) NAALAD2ATMKMT2AMAPTMDM4
SCHEMBL28088781 0.89 MAPT (0.50) NAALAD2ATMKMT2AMAPTMDM4
SCHEMBL8680909 0.89 MAPT (0.50) NAALAD2ATMKMT2AMAPTMDM4
Potassium Ion SCHEMBL6129087 0.88 CA12 (0.43) FOLH1CA12CA1CA2CA7
SCHEMBL9302196 0.88 CA12 (0.43) FOLH1CA12CA1CA2CA7
Potassium Ion SCHEMBL4826211 0.88 CA12 (0.43) FOLH1CA12CA1CA2CA7
Potassium Ion SCHEMBL31198116 0.88 CA12 (0.43) FOLH1CA12CA1CA2CA7
SCHEMBL8624954 0.88 MAPT (0.49) NAALAD2ATMKMT2AMAPTMDM4
SCHEMBL5995942 0.86 FOLH1 (0.47) FOLH1CA12CA1CA2CA7

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7622577-B2 Processes for the preparation of cephalosporin derivatives CJ CHEILJEDANG CORPORATION (KR) 2009-11-24 US disclosed
US-20090221815-A1 PROCESSES FOR THE PREPARATION OF CEPHEM DERIVATIVES CJ CHEILJEDANG CORPORATION (KR) 2009-09-03 US disclosed
US-7544797-B2 Processes for the preparation of cephem derivatives CJ CHEILJEDANG CORPORATION (KR) 2009-06-09 US disclosed
EP-1678187-A4 PROCESSES FOR THE PREPARATION OF CEPHALOSPORIN DERIVATIVES CJ CORP (KR) 2007-06-13 EP disclosed
EP-1678186-A4 PROCESSES FOR THE PREPARATION OF CEPHEM DERIVATIVES CJ CORP (KR) 2007-04-25 EP disclosed
US-20070083042-A1 Processes for the preparation of cephalosporin derivatives CJ CORPORATION (KR) 2007-04-12 US disclosed
US-20070060747-A1 Processes for the preparation of cephem derivatives CJ CORPORATION (KR) 2007-03-15 US disclosed
US-20060173176-A1 Process for the preparation of (z)-isomer enriched 7-amino-3-propen-1-yl-3-cephem-4-carboxylic acid RANBAXY LABORATORIES LIMITED (IN) 2006-08-03 US disclosed
EP-1678187-A1 PROCESSES FOR THE PREPARATION OF CEPHALOSPORIN DERIVATIVES CJ Corporation (KR) 2006-07-12 EP disclosed
EP-1678186-A1 PROCESSES FOR THE PREPARATION OF CEPHEM DERIVATIVES CJ Corporation (KR) 2006-07-12 EP disclosed
EP-1554288-A1 PROCESS FOR THE PREPARATION OF (Z)-ISOMER ENRICHED 7-AMINO-3-PROPEN-1-YL-3-CEPHEM-4- CARBOXYLIC ACID RANBAXY LABORATORIES, LTD. (IN) 2005-07-20 EP disclosed
WO-2005042544-A1 PROCESSES FOR THE PREPARATION OF CEPHALOSPORIN DERIVATIVES CJ CORPORATION (KR) 2005-05-12 WO disclosed
WO-2005042543-A1 PROCESSES FOR THE PREPARATION OF CEPHEM DERIVATIVES CJ CORPORATION (KR) 2005-05-12 WO disclosed
WO-2004033464-A1 PROCESS FOR THE PREPARATION OF (Z)-ISOMER ENRICHED 7-AMINO-3-PROPEN-1-YL-3-CEPHEM-4- CARBOXYLIC ACID RANBAXY LABORATORIES LIMITED (IN) 2004-04-22 WO disclosed
EP-0437566-B1 PHENYL-GLYCINE DERIVATIVES CHINOIN GYOGYSZER ES VEGYESZET (HU) 1994-09-28 EP disclosed
US-5338868-A Reacting glycine derivative with trifluoro methane sulfonic acid derivative at low temperature CHINOIN GYOGYSZER- ES VEGYESZETI TERMEKEK GYARA RT. (HU) 1994-08-16 US disclosed
US-4072710-A FROM SILYL ESTER AND THIONYL CHLORIDE PALOMO COLL A L 1978-02-07 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 (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-20070060747-A1 Processes for the preparation of cephem derivatives CEP170, HAMP, NISCH FOLH1 781/4885CA12 251/4885CA1 2056/4885
US-20070083042-A1 Processes for the preparation of cephalosporin derivatives ADH1C, HSD17B14, ADH1A FOLH1 1103/4885CA12 1491/4885CA1 2219/4885
US-20060173176-A1 Process for the preparation of (z)-isomer enriched 7-amino-3-propen-1-yl-3-cephem-4-carboxylic acid CPNE4, PAH, ALAD FOLH1 173/4885CA12 689/4885CA1 1069/4885
US-20090221815-A1 PROCESSES FOR THE PREPARATION OF CEPHEM DERIVATIVES CEP170, HAMP, NISCH FOLH1 781/4885CA12 251/4885CA1 2056/4885

“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.