SCHEMBL1147073

SCHEMBL1147073

NC(=O)NC(CCO)C(=O)O

nearest known ligand 0.47

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
TGFBR1 P36897 3/20 0.47
FOLH1 Q04609 6/20 0.43
NAALAD2 Q9Y3Q0 3/20 0.43
RIMKLA Q8IXN7 1/20 0.43
GNPAT O15228 1/20 0.38
KMT2A Q03164 1/20 0.36
CAD P27708 1/20 0.35
KDM4E B2RXH2 1/20 0.34
MAPT P10636 1/20 0.34
THRB P10828 1/20 0.34
ALOX15 P16050 1/20 0.34
NFKB1 P19838 1/20 0.34
PTGS2 P35354 1/20 0.34
THPO P40225 1/20 0.34
RECQL P46063 1/20 0.34
BLM P54132 1/20 0.34
SMN1; SMN2 Q16637 1/20 0.34

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
SCHEMBL1147075 1.00 TGFBR1 (0.47) TGFBR1FOLH1NAALAD2RIMKLAGNPAT
SCHEMBL12461743 0.84 GNPAT (0.52) TGFBR1FOLH1NAALAD2RIMKLAGNPAT
SCHEMBL2793959 0.81 TGFBR1 (0.68) TGFBR1FOLH1NAALAD2RIMKLACAD
SCHEMBL2307007 0.81 TGFBR1 (0.68) TGFBR1FOLH1NAALAD2RIMKLACAD
SCHEMBL2793957 0.81 TGFBR1 (0.68) TGFBR1FOLH1NAALAD2RIMKLACAD
SCHEMBL7043592 0.80 KMT2A (0.53) TGFBR1FOLH1NAALAD2RIMKLAKMT2A
SCHEMBL215383 0.80 FOLH1 (0.44) TGFBR1FOLH1NAALAD2RIMKLAGNPAT
SCHEMBL3282950 0.80 FPR2 (0.46) TGFBR1FOLH1NAALAD2RIMKLACAD
SCHEMBL5493511 0.80 KMT2A (0.53) TGFBR1FOLH1NAALAD2RIMKLAKMT2A
SCHEMBL215384 0.80 FOLH1 (0.44) TGFBR1FOLH1NAALAD2RIMKLAGNPAT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7884240-B2 Acylating L- or D-homoserine to produce N-acyl- L and/or D-homoserine lactone, opening the lactone ring and sulfiding with methyl mercaptan in the presence of a basic or acid catalyst, and hydrolyzing the product to remove the acyl group EVONIK DEGUSSA GMBH (DE) 2011-02-08 US claimed
EP-1976827-A2 METHOD FOR PRODUCING METHIONINE FROM HOMOSERINE Evonik Degussa GmbH (DE) 2008-10-08 EP claimed
US-20080146840-A1 Method for production of methionine from homoserine DEGUSSA GMBH (DE) 2008-06-19 US claimed
US-7368600-B2 Method for production of methionine from homoserine DEGUSSA GMBH (DE) 2008-05-06 US claimed
US-20070190622-A1 Method for production of methionine from homoserine DEGUSSA GMBH (DE) 2007-08-16 US claimed
WO-2007085514-A2 METHOD FOR PRODUCING METHIONINE FROM HOMOSERINE EVONIK DEGUSSA GMBH (DE) 2007-08-02 WO claimed
CN-112574118-B Process for preparing glufosinate-hydantoin intermediates and analogues 利尔化学股份有限公司 2023-10-31 CN disclosed
WO-2021057945-A1 METHOD FOR PREPARING GLUFOSINATE-AMMONIUM HYDANTOIN INTERMEDIATE AND ANALOGUE THEREOF 利尔化学股份有限公司 2021-04-01 WO disclosed
US-7884240-B2 Acylating L- or D-homoserine to produce N-acyl- L and/or D-homoserine lactone, opening the lactone ring and sulfiding with methyl mercaptan in the presence of a basic or acid catalyst, and hydrolyzing the product to remove the acyl group EVONIK DEGUSSA GMBH (DE) 2011-02-08 US disclosed
US-7884240-B2 Acylating L- or D-homoserine to produce N-acyl- L and/or D-homoserine lactone, opening the lactone ring and sulfiding with methyl mercaptan in the presence of a basic or acid catalyst, and hydrolyzing the product to remove the acyl group EVONIK DEGUSSA GMBH (DE) 2011-02-08 US disclosed
US-7884240-B2 Acylating L- or D-homoserine to produce N-acyl- L and/or D-homoserine lactone, opening the lactone ring and sulfiding with methyl mercaptan in the presence of a basic or acid catalyst, and hydrolyzing the product to remove the acyl group EVONIK DEGUSSA GMBH (DE) 2011-02-08 US disclosed
EP-1976827-A2 METHOD FOR PRODUCING METHIONINE FROM HOMOSERINE Evonik Degussa GmbH (DE) 2008-10-08 EP disclosed
EP-1976827-A2 METHOD FOR PRODUCING METHIONINE FROM HOMOSERINE Evonik Degussa GmbH (DE) 2008-10-08 EP disclosed
US-7368600-B2 Method for production of methionine from homoserine DEGUSSA GMBH (DE) 2008-05-06 US disclosed
US-20070190622-A1 Method for production of methionine from homoserine DEGUSSA GMBH (DE) 2007-08-16 US disclosed
US-20070190622-A1 Method for production of methionine from homoserine DEGUSSA GMBH (DE) 2007-08-16 US disclosed
US-20070190622-A1 Method for production of methionine from homoserine DEGUSSA GMBH (DE) 2007-08-16 US disclosed
WO-2007085514-A2 METHOD FOR PRODUCING METHIONINE FROM HOMOSERINE EVONIK DEGUSSA GMBH (DE) 2007-08-02 WO disclosed
WO-2007085514-A2 METHOD FOR PRODUCING METHIONINE FROM HOMOSERINE EVONIK DEGUSSA GMBH (DE) 2007-08-02 WO disclosed
WO-2007085514-A2 METHOD FOR PRODUCING METHIONINE FROM HOMOSERINE EVONIK DEGUSSA GMBH (DE) 2007-08-02 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-20080146840-A1 Method for production of methionine from homoserine MTR, BHMT2, BHMT TGFBR1 4141/4885FOLH1 471/4885NAALAD2 472/4885

“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.