SCHEMBL5055941

SCHEMBL5055941

CCC#CCCCCCCCC[O]

nearest known ligand 0.40

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
PTPN7 P35236 5/20 0.40
HMGCR P04035 3/20 0.40
RAB9A P51151 1/20 0.39
RECQL P46063 2/20 0.36
TDP1 Q9NUW8 2/20 0.36
KDM4E B2RXH2 2/20 0.33
ALDH1A1 P00352 2/20 0.33
HPGD P15428 2/20 0.33
MEN1 O00255 1/20 0.33
USP2 O75604 1/20 0.33
POLB P06746 1/20 0.33
MAPT P10636 1/20 0.33
ALOX12 P18054 1/20 0.33
BLM P54132 1/20 0.33
KMT2A Q03164 1/20 0.33
MCL1 Q07820 1/20 0.33
SMN1; SMN2 Q16637 1/20 0.33
EPHX2 P34913 3/20 0.32

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
SCHEMBL5056482 1.00 PTPN7 (0.40) PTPN7HMGCRRAB9ARECQLTDP1
SCHEMBL5056445 1.00 PTPN7 (0.40) PTPN7HMGCRRAB9ARECQLTDP1
SCHEMBL5056000 1.00 PTPN7 (0.40) PTPN7HMGCRRAB9ARECQLTDP1
SCHEMBL5056488 0.97
SCHEMBL2710122 0.89
SCHEMBL31336402 0.86 RAB9A (0.48) PTPN7HMGCRRAB9ARECQLTDP1
SCHEMBL7140331 0.84 PTPN7 (0.50) PTPN7HMGCRRAB9ARECQLTDP1
SCHEMBL5055925 0.84 PTPN7 (0.50) PTPN7HMGCRRAB9ARECQLTDP1
SCHEMBL5057471 0.84 PTPN7 (0.45) PTPN7HMGCRRAB9ARECQLTDP1
SCHEMBL5053259 0.84 PTPN7 (0.56) PTPN7HMGCRRAB9ARECQLTDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1756271-B1 METHODS FOR OBTAINING OPTICALLY ACTIVE EPOXIDES AND VICINAL DIOLS FROM 2,2-DISUBSTITUTED EPOXIDES CSIR (ZA) 2015-12-09 EP disclosed
EP-1753862-B1 METHODS FOR OBTAINING OPTICALLY ACTIVE EPOXIDES AND VICINAL DIOLS FROM MESO-EPOXIDES CSIR (ZA) 2015-11-18 EP disclosed
US-20080286832-A1 Methods for Obtaining Optically Active Epoxides and Vicinal Diols From 2,2-Disubstituted Epoxides COUNCIL FOR SCIENTIFIC AND INDUSTRIAL RESEARCH (ZA) 2008-11-20 US disclosed
US-20080199912-A1 Methods for Obtaining Optically Active Epoxides and Diols from 2,3-Disubstituted and 2,3-Trisubstituted Epoxides OXYRANE (UK) LTD. (GB) 2008-08-21 US disclosed
EP-1896597-A2 METHODS FOR OBTAINING OPTICALLY ACTIVE EPOXIDES AND DIOLS FROM 2,3-DISUBSTITUTED AND 2,3-TRISUBSTITUTED EPOXIDES CSIR (ZA) 2008-03-12 EP disclosed
US-20070275448-A1 Methods For Obtaining Optically Active Epoxides And Vicinal Diols From Meso-Epoxides CSIR (ZA) 2007-11-29 US disclosed
WO-2007069079-A2 METHODS FOR OBTAINING OPTICALLY ACTIVE EPOXIDES AND DIOLS FROM 2,3-DISUBSTITUTED AND 2,3-TRISUBSTITUTED EPOXIDES CSIR (US) 2007-06-21 WO disclosed
EP-1756271-A2 METHODS FOR OBTAINING OPTICALLY ACTIVE EPOXIDES AND VICINAL DIOLS FROM 2,2-DISUBSTITUTED EPOXIDES CSIR (ZA) 2007-02-28 EP disclosed
EP-1753862-A2 METHODS FOR OBTAINING OPTICALLY ACTIVE EPOXIDES AND VICINAL DIOLS FROM MESO-EPOXIDES CSIR (ZA) 2007-02-21 EP disclosed
WO-2005100587-A2 METHODS FOR OBTAINING OPTICALLY ACTIVE EPOXIDES AND VICINAL DIOLS FROM 2,2-DISUBSTITUTED EPOXIDES CSIR (ZA) 2005-10-27 WO disclosed
WO-2005100578-A2 METHODS FOR OBTAINING OPTICALLY ACTIVE EPOXIDES AND VICINAL DIOLS FROM MESO-EPOXIDES CSIR (ZA) 2005-10-27 WO 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 (3 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-20080199912-A1 Methods for Obtaining Optically Active Epoxides and Diols from 2,3-Disubstituted and 2,3-Trisubstituted Epoxides EPHX2, ERG28, EPHX1 PTPN7 4861/4885HMGCR 1301/4885RAB9A 3483/4885
US-20070275448-A1 Methods For Obtaining Optically Active Epoxides And Vicinal Diols From Meso-Epoxides EPHX2, EPHX1, DHODH PTPN7 4673/4885HMGCR 827/4885RAB9A 2930/4885
US-20080286832-A1 Methods for Obtaining Optically Active Epoxides and Vicinal Diols From 2,2-Disubstituted Epoxides EPHX2, ERG28, DERA PTPN7 4868/4885HMGCR 1703/4885RAB9A 3228/4885

“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.