SCHEMBL143910

SCHEMBL143910

CC(=O)NC(C(=O)O)C(=O)O

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 2/20 0.48
THRB P10828 2/20 0.48
RECQL P46063 2/20 0.48
NFKB1 P19838 2/20 0.48
MAPT P10636 2/20 0.48
ALOX15 P16050 1/20 0.48
PTGS2 P35354 1/20 0.48
THPO P40225 1/20 0.48
BLM P54132 1/20 0.48
SMN1; SMN2 Q16637 1/20 0.48
ALDH1A1 P00352 3/20 0.46
FNTA P49354 2/20 0.39
FNTB P49356 2/20 0.39
CA2 P00918 1/20 0.37
PTGS1 P23219 1/20 0.37
MMP12 P39900 1/20 0.37
MTNR1A P48039 3/20 0.36
MTNR1B P49286 3/20 0.36
FFAR3 O14843 1/20 0.35
LCK P06239 1/20 0.35

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
SCHEMBL9614381 0.97 KDM4E (0.46) KDM4ETHRBRECQLNFKB1MAPT
Butane SCHEMBL5183779 0.89 KDM4E (0.46) KDM4ETHRBRECQLNFKB1MAPT
SCHEMBL3869217 0.88 KDM4E (0.44) KDM4ETHRBRECQLNFKB1MAPT
SCHEMBL9336407 0.88 KDM4E (0.44) KDM4ETHRBRECQLNFKB1MAPT
SCHEMBL24938422 0.84 KDM4E (0.41) KDM4ETHRBRECQLNFKB1MAPT
SCHEMBL2165150 0.84 ALOX15 (0.41) KDM4ETHRBRECQLNFKB1MAPT
SCHEMBL6986221 0.82 SMN1; SMN2 (0.40) KDM4ETHRBRECQLNFKB1MAPT
SCHEMBL17483032 0.82 SMN1; SMN2 (0.40) KDM4ETHRBRECQLNFKB1MAPT
SCHEMBL27842807 0.80 MAPT (0.43) KDM4ETHRBRECQLNFKB1MAPT
SCHEMBL6118521 0.80 MAPT (0.43) KDM4ETHRBRECQLNFKB1MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118685774-A Cu-MTD etching solution for liquid crystal display panel and preparation method thereof 四川江化微电子材料有限公司 2024-09-24 CN claimed
CN-108383744-A A kind of preparation method of 2,6- dimethyl-tyrosine 浙江工业大学 2018-08-10 CN claimed
CN-105712901-B A kind of synthetic method of the nonenoic acid dicyclohexyl amine salt of 2 amino of optical activity intermediate N tertbutyloxycarbonyls 8 成都柏睿泰生物科技有限公司 2017-07-14 CN claimed
CN-106606423-A Chitosan water-soluble combination agent and application thereof 李建明 2017-05-03 CN claimed
CN-105712901-A Method for synthesizing optically active intermediate N-tert-butoxycarbonyl-2-amino-8-nonenoic dicyclohexylamine salt 成都柏睿泰生物科技有限公司 2016-06-29 CN claimed
US-20160031800-A1 SYNTHESIS OF CHIRAL KYNURENINE COMPOUNDS AND INTERMEDIATES VISTAGEN THERAPEUTICS, INC. 2016-02-04 US claimed
EP-2970080-A1 SYNTHESIS OF CHIRAL KYNURENINE COMPOUNDS AND INTERMEDIATES Vistagen Therapeutics, Inc. (US) 2016-01-20 EP claimed
WO-2014152835-A1 SYNTHESIS OF CHIRAL KYNURENINE COMPOUNDS AND INTERMEDIATES VISTAGEN THERAPEUTICS, INC. (US) 2014-09-25 WO claimed
EP-0663899-B1 SUBSTITUTED KYNURENINES, A PROCESS FOR THEIR PREPARATION, AND USE AS MEDICAMENTS UNIV MARYLAND (US) 1999-06-30 EP claimed
EP-0919538-A1 Substituted kynurenines, a process for their preparation, and use as medicaments THE UNIVERSITY OF MARYLAND AT BALTIMORE (US) 1999-06-02 EP claimed
EP-0663899-A4 SUBSTITUTED KYNURENINES, A PROCESS FOR THEIR PREPARATION, AND USE AS MEDICAMENTS. UNIV MARYLAND (US) 1996-01-17 EP claimed
EP-0663899-A1 SUBSTITUTED KYNURENINES, A PROCESS FOR THEIR PREPARATION, AND USE AS MEDICAMENTS THE UNIVERSITY OF MARYLAND AT BALTIMORE (US) 1995-07-26 EP claimed
WO-1995004714-A1 SUBSTITUTED KYNURENINES, A PROCESS FOR THEIR PREPARATION, AND USE AS MEDICAMENTS UNIVERSITY OF MARYLAND AT BALTIMORE (US) 1995-02-16 WO claimed
EP-0231709-B1 PHENYL NAPHTHYRIDINES, WITH A FUNCTIONAL GROUP IN POSITION 3, PROCESS FOR THEIR PREPARATION, MEDICAMENTS CONTAINING THEM, ESPECIALLY AS ANTI-ULCERS LABORATOIRES UPSA (FR) 1992-07-22 EP claimed
EP-0242709-A2 Antagonists of specific excitatory amino acid neurotransmitter receptors NOVA PHARMACEUTICAL CORPORATION (US) 1987-10-28 EP claimed
EP-0003335-B1 PROCESS FOR PREPARING AMINOMALONIC ACID DINITRILE TOSYLAT OR ACETYLAMINOMALONIC ACID DINITRIL LONZA AG (CH) 1981-07-01 EP claimed
US-12612421-B2 Method for producing 4-borono-L-phenylalanine and intermediate thereof STELLA PHARMA CORPORATION (JP) 2026-04-28 US disclosed
CN-118685774-B Cu-MTD etching solution for liquid crystal display panel and preparation method thereof 四川江化微电子材料有限公司 2024-12-27 CN disclosed
US-4084057-A Process for the production of 4-acylamido-4, 4-dicarbalkoxy-butanalphenylhydrazone DEUTSCHE GOLD- UND SILBER-SCHEIDEANSTALT VORMALS ROESSLER (DT) 1978-04-11 US disclosed
US-4073795-A Synthesis of tryptophans HOFFMANN-LA ROCHE INC. (US) 1978-02-14 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 (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-12612421-B2 Method for producing 4-borono-L-phenylalanine and intermediate thereof BCAT2, BCAT1, CLIC4 KDM4E 3078/4885THRB 106/4885RECQL 4114/4885
US-20160031800-A1 SYNTHESIS OF CHIRAL KYNURENINE COMPOUNDS AND INTERMEDIATES KYNU, KMO, AADAT KDM4E 749/4885THRB 2839/4885RECQL 2265/4885

“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.