SCHEMBL5708342

SCHEMBL5708342

O=C(O)C[C@H](O)CNC(=O)OCc1ccccc1

nearest known ligand 0.56

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
HTT P42858 1/20 0.56
LMNA P02545 1/20 0.55
SMN1; SMN2 Q16637 1/20 0.55
CASP1 P29466 12/20 0.52
ALDH1A1 P00352 1/20 0.49
SYK P43405 1/20 0.48
SLC6A2 P23975 1/20 0.47
SLC6A3 Q01959 1/20 0.47
KMT2A Q03164 1/20 0.47
TDP1 Q9NUW8 1/20 0.47

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
SCHEMBL222634 1.00 HTT (0.56) HTTLMNASMN1; SMN2CASP1ALDH1A1
SCHEMBL5019087 0.91 LMNA (0.61) HTTLMNASMN1; SMN2ALDH1A1SYK
SCHEMBL223222 0.90 LMNA (0.54) HTTLMNASMN1; SMN2CASP1ALDH1A1
SCHEMBL20530482 0.88 ALDH1A1 (0.54) HTTLMNASMN1; SMN2ALDH1A1SYK
SCHEMBL19615746 0.88 LMNA (0.52) HTTLMNASMN1; SMN2CASP1ALDH1A1
SCHEMBL19615744 0.88 LMNA (0.52) HTTLMNASMN1; SMN2CASP1ALDH1A1
SCHEMBL30642172 0.87 LMNA (0.51) HTTLMNASMN1; SMN2CASP1ALDH1A1
SCHEMBL334682 0.86 LMNA (0.56) HTTLMNASMN1; SMN2ALDH1A1SYK
SCHEMBL1569295 0.86 LMNA (0.56) HTTLMNASMN1; SMN2ALDH1A1SYK
SCHEMBL12067897 0.86 LMNA (0.56) HTTLMNASMN1; SMN2ALDH1A1SYK

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
WO-2023220715-A1 OXOINDOLINYL AMIDE DERIVATIVES FOR INHIBITING NLRP3 AND USES THEREOF VENTUS THERAPEUTICS U.S., INC. (US) 2023-11-16 WO disclosed
EP-1008590-B1 Process for preparing optically active oxazolidinone derivatives TAKASAGO PERFUMERY CO LTD (JP) 2006-10-11 EP disclosed
US-6403804-B1 ALLOWING HYDRAZINE TO REACT ON OPTICALLY ACTIVE ACID ESTER HAVING HYDROXYL GROUP AT 3-POSITION TO GIVE OPTICALLY ACTIVE HYDRAZIDE HAVING HYDROXYL GROUP AT 3-POSITION, SUBJECTING OPTICALLY ACTIVE HYDRAZIDE TO CURTIUS REARRANGEMENT TAKASAGO INTERNATIONAL CORPORATION (JP) 2002-06-11 US disclosed
EP-1008590-A1 Process for preparing optically active oxazolidinone derivative Takasago International Corporation (JP) 2000-06-14 EP disclosed
EP-0787718-B1 Process for preparing optically active 4-hydroxy-2-pyrrolidone TAKASAGO PERFUMERY CO LTD (JP) 1999-09-08 EP disclosed
US-5837877-A Process for preparing optically active 4-hydroxy-2-pyrrolidone TAKASAGO INTERNATIONAL CORPORATION (JP) 1998-11-17 US disclosed
EP-0787718-A1 Process for preparing optically active 4-hydroxy-2-pyrrolidone Takasago International Corporation (JP) 1997-08-06 EP disclosed