SCHEMBL6015192

SCHEMBL6015192

O=C1CCN([C@H]2CC(O)[C@@H](CO)O2)C(=O)N1

nearest known ligand 0.58

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
CDA P32320 2/20 0.58
TK1 P04183 3/20 0.45
LMNA P02545 2/20 0.45
SMN1; SMN2 Q16637 2/20 0.45
ALOX12 P18054 1/20 0.43
ADRA1A P35348 1/20 0.43
ADRB1 P08588 1/20 0.42
DNMT1 P26358 1/20 0.42
TK2 O00142 1/20 0.42
CYP1A2 P05177 1/20 0.41
CYP3A4 P08684 1/20 0.41
TSHR P16473 1/20 0.41
BLM P54132 1/20 0.41
PMP22 Q01453 1/20 0.41
NPSR1 Q6W5P4 1/20 0.41

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
SCHEMBL658758 1.00 CDA (0.58) CDATK1LMNASMN1; SMN2ALOX12
SCHEMBL15893325 1.00 CDA (0.58) CDATK1LMNASMN1; SMN2ALOX12
SCHEMBL21423103 1.00 CDA (0.58) CDATK1LMNASMN1; SMN2ALOX12
SCHEMBL658757 1.00 CDA (0.58) CDATK1LMNASMN1; SMN2ALOX12
SCHEMBL4318242 1.00 CDA (0.58) CDATK1LMNASMN1; SMN2ALOX12
SCHEMBL15895803 1.00 CDA (0.58) CDATK1LMNASMN1; SMN2ALOX12
SCHEMBL31685506 0.81 TYMS (0.48)
SCHEMBL22916929 0.79 CDA (0.44) CDATK1TSHR
SCHEMBL23240762 0.78 CDA (0.58) CDATK1LMNASMN1; SMN2ALOX12
SCHEMBL172249 0.78 CDA (0.58) CDATK1LMNASMN1; SMN2ALOX12

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20040063926-A1 L-nucleic acid derivative and processes for the synthesis thereof MITSUI CHEMICALS, INC. (JP) 2004-04-01 US claimed
EP-1348712-A1 L-NUCLEIC ACID DERIVATIVES AND PROCESSES FOR THE SYNTHESIS THEREOF Mitsui Chemicals, Inc. (JP) 2003-10-01 EP claimed
US-20210196723-A1 Modulators of DUX4 for Regulation of Muscle Function SONIC MASTER LTD (VG) 2021-07-01 US disclosed
US-9283242-B2 Uses of dihydro bases MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) 2016-03-15 US disclosed
US-20140206639-A1 USES OF DIHYDRO BASES MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) 2014-07-24 US disclosed
US-7125983-B2 L-nucleic acid derivatives and process for the synthesis thereof MITSUI CHEMICALS, INC. (JP) 2006-10-24 US disclosed
US-20040063926-A1 L-nucleic acid derivative and processes for the synthesis thereof MITSUI CHEMICALS, INC. (JP) 2004-04-01 US disclosed
EP-1348712-A1 L-NUCLEIC ACID DERIVATIVES AND PROCESSES FOR THE SYNTHESIS THEREOF Mitsui Chemicals, Inc. (JP) 2003-10-01 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 (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-20140206639-A1 USES OF DIHYDRO BASES DPYD, DHODH, HPRT1 CDA 120/4885TK1 166/4885LMNA 701/4885
US-20210196723-A1 Modulators of DUX4 for Regulation of Muscle Function DDX21, MBNL1, MECP2 CDA 813/4885TK1 2815/4885LMNA 1943/4885
US-20040063926-A1 L-nucleic acid derivative and processes for the synthesis thereof TYMS, RNGTT, DTYMK CDA 72/4885TK1 23/4885LMNA 653/4885

“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.