SCHEMBL483916

SCHEMBL483916

CC(=O)NCC1CN(c2cccc(N3CCOC[C@@H]3F)c2)C(=O)O1

nearest known ligand 0.61

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
MAOA P21397 5/20 0.61
MAOB P27338 4/20 0.61
PTGS1 P23219 2/20 0.61
SDHA P31040 2/20 0.61
LMNA P02545 1/20 0.61
CALML3 P27482 1/20 0.61
F10 P00742 5/20 0.46
CYP1A2 P05177 1/20 0.45
CYP3A4 P08684 1/20 0.45
CYP2D6 P10635 1/20 0.45
CYP2C9 P11712 1/20 0.45
CYP2C19 P33261 1/20 0.45

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
SCHEMBL27707418 1.00 MAOA (0.61) MAOAMAOBPTGS1SDHALMNA
SCHEMBL27875818 1.00 MAOA (0.61) MAOAMAOBPTGS1SDHALMNA
SCHEMBL7790986 0.92 MAOB (0.53) MAOAMAOBPTGS1SDHALMNA
SCHEMBL28594529 0.90 MAOA (0.62) MAOAMAOBPTGS1SDHALMNA
SCHEMBL7537313 0.90 MAOA (0.62) MAOAMAOBPTGS1SDHALMNA
SCHEMBL7704124 0.90 MAOB (0.49) MAOAMAOBPTGS1SDHALMNA
SCHEMBL7157301 0.90 MAOB (0.49) MAOAMAOBPTGS1SDHALMNA
SCHEMBL6691779 0.90 MAOB (0.49) MAOAMAOBPTGS1SDHALMNA
SCHEMBL7157296 0.90 MAOB (0.49) MAOAMAOBPTGS1SDHALMNA
SCHEMBL6687197 0.88 F10 (0.48) MAOAMAOBPTGS1SDHALMNA

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 27 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20090156806-A1 Process for the Preparation of Oxazolidinone Derivatives DIPHARMA FRANCIS S.R.I. (IT) 2009-06-18 US claimed
WO-2013072923-A1 PROCESS FOR THE PREPARATION OF CRYSTALLINE LINEZOLID CADILA HEALTHCARE LIMITED (IN) 2013-05-23 WO disclosed
EP-2072505-B1 A process for the preparation of oxazolidinone derivatives DIPHARMA FRANCIS SRL (IT) 2012-02-01 EP disclosed
US-7989618-B2 Linezolid crystalline hydrate form and linezolid salts DIPHARMA FRANCIS S.R.L. (IT) 2011-08-02 US disclosed
EP-2174935-A1 Linezolid Compositions Teva Pharmaceutical Industries Ltd (IL) 2010-04-14 EP disclosed
EP-2072505-A3 A process for the preparation of oxazolidinone derivatives Dipharma Francis S.r.l. (IT) 2009-08-12 EP disclosed
EP-2072505-A2 A process for the preparation of oxazolidinone derivatives Dipharma Francis S.r.l. (IT) 2009-06-24 EP disclosed
EP-2072505-A2 A process for the preparation of oxazolidinone derivatives Dipharma Francis S.r.l. (IT) 2009-06-24 EP disclosed
US-20090156806-A1 Process for the Preparation of Oxazolidinone Derivatives DIPHARMA FRANCIS S.R.I. (IT) 2009-06-18 US disclosed
US-20090156806-A1 Process for the Preparation of Oxazolidinone Derivatives DIPHARMA FRANCIS S.R.I. (IT) 2009-06-18 US disclosed
US-7291614-B2 Processes for the preparation of linezolid intermediate TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2007-11-06 US disclosed
US-20070197529-A1 Isolated desfluoro-linezolid, preparation thereof and its use as a reference marker and standard TEVA PHARMACEUTICALS USA, INC. 2007-08-23 US disclosed
US-20070021417-A1 Processes for the preparation of linezolid intermediate TEVA PHARAMCEUTIALS USA, INC. 2007-01-25 US disclosed
US-20060258655-A1 Crystalline forms of linezolid intermediate TEVA PHARMACEUTICALS USA, INC. 2006-11-16 US disclosed
US-20060252932-A1 Isolated bis-linezolid, preparation thereof, and its use as a reference standard ENTIRE INTEREST 2006-11-09 US disclosed
WO-2006091848-A9 ISOLATED BIS-LINEZOLID, PREPARATION THEREOF, AND ITS USE AS A REFERENCE STANDARD TEVA PHARMA (IL) 2006-11-09 WO disclosed
WO-2006091731-A2 PROCESSES FOR THE PREPARATION OF LINEZOLID INTERMEDIATE TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2006-08-31 WO disclosed
WO-2006091777-A1 CRYSTALLINE FORMS OF LINEZOLID INTERMEDIATE TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2006-08-31 WO disclosed
US-20060142283-A1 Crystalline form IV of linezolid TEVA PHARMACEUTICALS USA, INC. 2006-06-29 US disclosed
US-20060111350-A1 Solid forms of linezolid and processes for preparation thereof TEVA PHARMACEUTICALS USA, INC. 2006-05-25 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 (7 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-20090156806-A1 Process for the Preparation of Oxazolidinone Derivatives OXA1L, AAAS, MLYCD MAOA 466/4885MAOB 648/4885PTGS1 3485/4885
US-20060142283-A1 Crystalline form IV of linezolid CYP4X1, MLX, CYP3A4 MAOA 1716/4885MAOB 2041/4885PTGS1 4015/4885
US-20070021417-A1 Processes for the preparation of linezolid intermediate CYP2C9, MRPL9, OXA1L MAOA 649/4885MAOB 688/4885PTGS1 4398/4885
US-20060111350-A1 Solid forms of linezolid and processes for preparation thereof F9, Q6ZSR9, TBCD MAOA 1756/4885MAOB 2551/4885PTGS1 4164/4885
US-20060252932-A1 Isolated bis-linezolid, preparation thereof, and its use as a reference standard FHIT, CYP2C9, CYP2C19 MAOA 2591/4885MAOB 2182/4885PTGS1 4246/4885
US-20070197529-A1 Isolated desfluoro-linezolid, preparation thereof and its use as a reference marker and standard MLLT3, DAO, FHIT MAOA 1747/4885MAOB 2084/4885PTGS1 4548/4885
US-20060258655-A1 Crystalline forms of linezolid intermediate EML4, MLLT3, OXA1L MAOA 1298/4885MAOB 1529/4885PTGS1 4511/4885

“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.