SCHEMBL4923256

SCHEMBL4923256

NC(O)C[C@H](O)CC(=O)OCc1ccccc1

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SLC15A1 P46059 2/20 0.53
ALDH1A1 P00352 3/20 0.53
MAPK1 P28482 1/20 0.53
L3MBTL1 Q9Y468 1/20 0.53
KMT2A Q03164 2/20 0.45
SLC6A2 P23975 1/20 0.45
SLC6A3 Q01959 1/20 0.45
TDP1 Q9NUW8 1/20 0.45
NPC1 O15118 1/20 0.45
CDC25B P30305 1/20 0.44
LTA4H P09960 1/20 0.44
LAP3 P28838 1/20 0.44
ABCB1 P08183 1/20 0.43
SLC1A1 P43005 4/20 0.43
SLC1A3 P43003 3/20 0.43
SLC1A2 P43004 2/20 0.43
MEN1 O00255 1/20 0.43
CYP1A2 P05177 1/20 0.43
CYP2D6 P10635 1/20 0.43
CYP2C9 P11712 1/20 0.43

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
SCHEMBL6546883 0.87 ALDH1A1 (0.59) SLC15A1ALDH1A1MAPK1L3MBTL1KMT2A
SCHEMBL6153568 0.87 ALDH1A1 (0.63) SLC15A1ALDH1A1MAPK1L3MBTL1KMT2A
SCHEMBL4653510 0.84 ALDH1A1 (0.56) SLC15A1ALDH1A1MAPK1L3MBTL1KMT2A
Hydrochloric Acid SCHEMBL6178180 0.83 ALDH1A1 (0.54) SLC15A1ALDH1A1MAPK1L3MBTL1KMT2A
SCHEMBL14994287 0.83 ALDH1A1 (0.54) SLC15A1ALDH1A1MAPK1L3MBTL1KMT2A
SCHEMBL9193055 0.83 ALDH1A1 (0.54) SLC15A1ALDH1A1MAPK1L3MBTL1KMT2A
SCHEMBL14993140 0.83 ALDH1A1 (0.54) SLC15A1ALDH1A1MAPK1L3MBTL1KMT2A
SCHEMBL5829150 0.82 ALDH1A1 (0.58) SLC15A1ALDH1A1MAPK1L3MBTL1KMT2A
SCHEMBL25622569 0.82 ALDH1A1 (0.58) SLC15A1ALDH1A1MAPK1L3MBTL1KMT2A
SCHEMBL27461581 0.81 ALDH1A1 (0.53) SLC15A1ALDH1A1MAPK1L3MBTL1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7390825-B1 Process for the preparation of oxazolidinones and method of use thereof BOARD OF TRUSTEES OF MICHIGAN STATE UNIVERSITY (US) 2008-06-24 US disclosed
US-20080146458-A1 PROCESS FOR THE PREPARATION OF OXAZOLIDINONES AND METHOD OF USE THEREOF BOARD OF TRUSTEES OF MICHIGAN STATE UNIVERSITY (US) 2008-06-19 US disclosed
US-20070265451-A1 Process for the preparation of oxazolidinones and method of use thereof BOARD OF TRUSTEES OF MICHIGAN STATE UNIVERSITY (US) 2007-11-15 US disclosed
EP-1578723-A4 PROCESS FOR THE PREPARATION OF OXAZOLIDINONES AND METHOD OF USE THEREOF UNIV MICHIGAN STATE (US) 2006-11-02 EP disclosed
EP-1578723-A3 PROCESS FOR THE PREPARATION OF OXAZOLIDINONES AND METHOD OF USE THEREOF MICHIGAN STATE UNIVERSITY (US) 2005-10-20 EP disclosed
EP-1578723-A2 PROCESS FOR THE PREPARATION OF OXAZOLIDINONES AND METHOD OF USE THEREOF MICHIGAN STATE UNIVERSITY (US) 2005-09-28 EP disclosed
WO-2003106413-A2 PROCESS FOR THE PREPARATION OF OXAZOLIDINONES AND METHOD OF USE THEREOF MICHIGAN STATE UNIVERSITY (US) 2003-12-24 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 (2 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-20070265451-A1 Process for the preparation of oxazolidinones and method of use thereof OXA1L, OTC, ODC1 SLC15A1 4178/4885ALDH1A1 2186/4885MAPK1 2823/4885
US-20080146458-A1 PROCESS FOR THE PREPARATION OF OXAZOLIDINONES AND METHOD OF USE THEREOF OXA1L, OGFOD1, CYP51A1 SLC15A1 4124/4885ALDH1A1 1117/4885MAPK1 2215/4885

“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.