SCHEMBL2072883

SCHEMBL2072883

C[C@H](CO)CCCOCc1ccccc1

nearest known ligand 0.45

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 1/20 0.45
L3MBTL1 Q9Y468 2/20 0.44
TDP1 Q9NUW8 1/20 0.44
GBA1 P04062 2/20 0.42
UGCG Q16739 2/20 0.42
GBA2 Q9HCG7 2/20 0.42
MMP3 P08254 2/20 0.41
MMP1 P03956 1/20 0.41
TRPA1 O75762 3/20 0.41
HTT P42858 1/20 0.40
SMN1; SMN2 Q16637 1/20 0.40
CA1 P00915 1/20 0.40
CA2 P00918 1/20 0.40
CA7 P43166 1/20 0.40
CA9 Q16790 1/20 0.40
HRH4 Q9H3N8 1/20 0.40
HRH3 Q9Y5N1 1/20 0.40
MMP9 P14780 1/20 0.40
MMP8 P22894 1/20 0.40
KDM4E B2RXH2 1/20 0.40

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
SCHEMBL3485268 1.00 TSHR (0.45) TSHRL3MBTL1TDP1GBA1UGCG
SCHEMBL3485267 1.00 TSHR (0.45) TSHRL3MBTL1TDP1GBA1UGCG
SCHEMBL13986787 0.95 L3MBTL1 (0.47) TSHRL3MBTL1TDP1GBA1UGCG
SCHEMBL11121387 0.90 TSHR (0.48) TSHRL3MBTL1TDP1TRPA1HTT
SCHEMBL28425565 0.90 TSHR (0.48) TSHRL3MBTL1TDP1TRPA1HTT
SCHEMBL27894678 0.90 TSHR (0.48) TSHRL3MBTL1TDP1TRPA1HTT
SCHEMBL27622932 0.85 TSHR (0.47) TSHRL3MBTL1TDP1GBA1UGCG
SCHEMBL27622935 0.85 TSHR (0.47) TSHRL3MBTL1TDP1GBA1UGCG
SCHEMBL13573008 0.84 KMT2A (0.43) TSHRL3MBTL1TDP1MMP3MMP1
SCHEMBL10081323 0.83 L3MBTL1 (0.54) TSHRL3MBTL1TDP1GBA1UGCG

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7893268-B2 Epithiolone analogues UNIVERSITY OF TOLEDO (US) 2011-02-22 US disclosed
US-20100003732-A1 PROCESS FOR PRODUCTION OF OPTICALLY ACTIVE 2-SUBSTITUTED PROPANAL DERIVATIVE KANEKA CORPORATION (JP) 2010-01-07 US disclosed
US-20090258904-A1 Epithiolone Analogues UNIVERSITY OF TOLEDO 2009-10-15 US disclosed
EP-1887085-A1 PROCESS FOR PRODUCTION OF OPTICALLY ACTIVE 2-SUBSTITUTED PROPANAL DERIVATIVE Kaneka Corporation (JP) 2008-02-13 EP disclosed
WO-2007015929-A2 EPOTHILONE ANALOGUES UNIVERSITY OF TOLEDO (US) 2007-02-08 WO disclosed
EP-1080082-B1 INTERMEDIATES FOR THE SYNTHESIS OF EPOTHILONES AND METHODS FOR THEIR PREPARATION NOVARTIS AG (CH) 2004-10-06 EP disclosed
US-6350878-B1 BASIFICATION AND IODINATION OF ALDEHYDE NOVARTIS AG (CH) 2002-02-26 US disclosed
EP-1080082-A1 INTERMEDIATES FOR THE SYNTHESIS OF EPOTHILONES AND METHODS FOR THEIR PREPARATION Novartis AG (CH) 2001-03-07 EP disclosed
WO-1999059985-A1 INTERMEDIATES FOR THE SYNTHESIS OF EPOTHILONES AND METHODS FOR THEIR PREPARATION NOVARTIS AG (CH) 1999-11-25 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 (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-20090258904-A1 Epithiolone Analogues ESRRB, ESR2, ESRRA TSHR 2808/4885L3MBTL1 1005/4885TDP1 4297/4885

“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.