SCHEMBL7208303

SCHEMBL7208303

CCCCCCCCCCCC(=O)N[C@@H](CCC(=O)OC)C(=O)OC

nearest known ligand 0.64

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 3/20 0.64
NOD1 Q9Y239 7/20 0.57
POLB P06746 2/20 0.57
MEN1 O00255 1/20 0.51
FAAH O00519 1/20 0.51
MAPK1 P28482 1/20 0.51
DNM1 Q05193 1/20 0.50
PLA2G2C Q5R387 1/20 0.50
L3MBTL1 Q9Y468 1/20 0.49
PLA2G10 O15496 2/20 0.47
POLA1 P09884 1/20 0.46

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
SCHEMBL28083226 1.00 KMT2A (0.64) KMT2ANOD1POLBMEN1FAAH
SCHEMBL7761870 1.00 KMT2A (0.64) KMT2ANOD1POLBMEN1FAAH
SCHEMBL28083227 1.00 KMT2A (0.64) KMT2ANOD1POLBMEN1FAAH
SCHEMBL16465356 0.92 SLC6A5 (0.56) KMT2ANOD1POLB
SCHEMBL16465619 0.91 NOD1 (0.63) KMT2ANOD1POLBPLA2G2CPLA2G10
SCHEMBL10338745 0.89 KMT2A (0.52) KMT2ANOD1POLBMEN1FAAH
SCHEMBL10338747 0.89 KMT2A (0.52) KMT2ANOD1POLBMEN1FAAH
SCHEMBL23961855 0.89 NOD1 (0.58) KMT2ANOD1POLBMEN1FAAH
SCHEMBL8576701 0.89 NOD1 (0.62) KMT2ANOD1POLBMEN1FAAH
SCHEMBL8733276 0.89 NOD1 (0.62) KMT2ANOD1POLBMEN1FAAH

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0775690-B1 Process for the preparation of N-lauroyl-L-glutamic acid dimethylester CLARIANT GMBH (DE) 2001-06-20 EP claimed
EP-0795540-B1 Process for the preparation of N-Lauroyl-L-glutamic acid di-n-butylamide CLARIANT GMBH (DE) 1999-09-29 EP claimed
US-5792880-A Process for the preparation of N-lauroyl-L-glutamic acid di-n-butylamide HOECHST AKTIENGESELLSCHAFT (DE) 1998-08-11 US claimed
US-5726331-A Dimethyl n-lauroyl-l-glutamate HOECHST AKTIENGESELLSCHAFT (DE) 1998-03-10 US claimed
JP-9221461-A None JP disclosed
JP-10001463-A None JP disclosed
CN-1198795-C N-acyl amino-acid amide prodn. process AJINOMOTO KK (JP) 2005-04-27 CN disclosed
EP-1094059-B1 Process for production of N-acyl amino acid amide AJINOMOTO KK (JP) 2003-03-26 EP disclosed
US-6335468-B1 CONDENSING N-ACYL AMINO ACID OR SALT THEREOF WITH AMINE AND/OR AMMONIA UNDER DEHYDRATING CONDITIONS IN PRESENCE OF BORON COMPOUND AS CATALYST WITH ALCOHOL COEXISTENT AS AUXILIARY SOLVENT AJINOMOTO CO., INC. (JP) 2002-01-01 US disclosed
EP-0775690-B1 Process for the preparation of N-lauroyl-L-glutamic acid dimethylester CLARIANT GMBH (DE) 2001-06-20 EP disclosed
CN-1294121-A N-acyl amino-acid amide prodn. process AJINOMOTO KK (JP) 2001-05-09 CN disclosed
EP-1094059-A1 Process for production of N-acyl amino acid amide Ajinomoto Co., Inc. (JP) 2001-04-25 EP disclosed
US-5792880-A Process for the preparation of N-lauroyl-L-glutamic acid di-n-butylamide HOECHST AKTIENGESELLSCHAFT (DE) 1998-08-11 US disclosed
US-5792880-A Process for the preparation of N-lauroyl-L-glutamic acid di-n-butylamide HOECHST AKTIENGESELLSCHAFT (DE) 1998-08-11 US disclosed
US-5726331-A Dimethyl n-lauroyl-l-glutamate HOECHST AKTIENGESELLSCHAFT (DE) 1998-03-10 US disclosed
US-5726331-A Dimethyl n-lauroyl-l-glutamate HOECHST AKTIENGESELLSCHAFT (DE) 1998-03-10 US disclosed
JP-H101463-A PRODUCTION OF N-LAUROYL-L-GLUTAMIC ACID-DI-N-BUTYLAMIDE HOECHST AG 1998-01-06 JP disclosed
JP-H09221461-A PRODUCTION OF DIMETHYL N-LAUROYL-L-GLUTAMATE HOECHST AG 1997-08-26 JP disclosed
EP-0775690-A1 Process for the preparation of N-lauroyl-L-glutamic acid dimethylester HOECHST AKTIENGESELLSCHAFT (DE) 1997-05-28 EP disclosed
EP-0775690-A1 Process for the preparation of N-lauroyl-L-glutamic acid dimethylester HOECHST AKTIENGESELLSCHAFT (DE) 1997-05-28 EP disclosed