SCHEMBL2245383

SCHEMBL2245383

O=C1CC(C(=O)OCCNC(=O)OCc2ccccc2)C(=O)N1

nearest known ligand 0.55

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
LMNA P02545 1/20 0.55
SMN1; SMN2 Q16637 1/20 0.55
IDO1 P14902 2/20 0.51
TDO2 P48775 1/20 0.51
L3MBTL1 Q9Y468 2/20 0.49
MAPT P10636 1/20 0.49
HTT P42858 1/20 0.47
GAA P10253 1/20 0.46
MEN1 O00255 1/20 0.45
KMT2A Q03164 1/20 0.45
TGM2 P21980 1/20 0.43
GPBAR1 Q8TDU6 3/20 0.43
KEAP1 Q14145 2/20 0.42
NFE2L2 Q16236 2/20 0.42
ALDH1A1 P00352 1/20 0.41

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
SCHEMBL5227458 0.85 GPBAR1 (0.51) SMN1; SMN2GAAGPBAR1
SCHEMBL274968 0.85 GPBAR1 (0.51) SMN1; SMN2GAAGPBAR1
SCHEMBL28640796 0.82 IDO1 (0.49) LMNASMN1; SMN2IDO1TDO2L3MBTL1
SCHEMBL794256 0.82 IDO1 (0.49) LMNASMN1; SMN2IDO1TDO2L3MBTL1
SCHEMBL26276948 0.75 SMN1; SMN2 (0.62) LMNASMN1; SMN2L3MBTL1MAPTHTT
SCHEMBL5180974 0.74 NAAA (0.58) GAAGPBAR1ALDH1A1
SCHEMBL765661 0.74 NAAA (0.58) GAAGPBAR1ALDH1A1
SCHEMBL3930648 0.74 NAAA (0.58) GAAGPBAR1ALDH1A1
SCHEMBL8777371 0.74 KMT2A (0.48) MEN1KMT2AGPBAR1
SCHEMBL8745681 0.74 IDO1 (0.47) LMNASMN1; SMN2IDO1TDO2L3MBTL1

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 6 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7994342-B2 Method for producing optically active succinimide compound NISSAN CHEMICAL INDUSTRIES, LTD. (JP) 2011-08-09 US disclosed
US-7807846-B2 such as 2-benzyloxycarbonylamino-2-ethoxycarbonyl succinimide by reacting aminomalonic ester with halo-containing amide in solvent (ethanol) in presence of sodium ethoxide; intermediates, raw materials for industrial scale production of drugs; cost efficiency NISSAN CHEMICAL INDUSTRIES, LTD. (JP) 2010-10-05 US disclosed
US-20100003729-A1 Method for producing optically active succinimide compound NISSAN CHEMICAL INDUSTRIES, LTD. (JP) 2010-01-07 US disclosed
US-20100004464-A1 Method for producing succinimide compound NISSAN CHEMICAL INDUSTRIES, LTD. (JP) 2010-01-07 US disclosed
EP-2077261-A1 METHOD FOR PRODUCING SUCCINIMIDE COMPOUND Nissan Chemical Industries, Ltd. (JP) 2009-07-08 EP disclosed
EP-2071033-A1 METHOD FOR PRODUCING OPTICALLY ACTIVE SUCCINIMIDE COMPOUND Nissan Chemical Industries, Ltd. (JP) 2009-06-17 EP 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-20100004464-A1 Method for producing succinimide compound ALDH7A1, SDHB, SDHA LMNA 2353/4885SMN1; SMN2 445/4885IDO1 3375/4885

“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.