SCHEMBL18709397

SCHEMBL18709397

O=C(Nc1ccc(S(=O)(=O)NC2CCOC2=O)cc1)c1ccc([N+](=O)[O-])o1

nearest known ligand 0.61

Predicted protein targets (top 5)

geneUniProtsupporting neighboursconfidence
DDIT3 P35638 13/20 0.61
RAB9A P51151 2/20 0.56
MAPT P10636 1/20 0.56
KMT2A Q03164 1/20 0.56
NPC1 O15118 1/20 0.52

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
SCHEMBL20296955 1.00 DDIT3 (0.61) DDIT3RAB9AMAPTKMT2ANPC1
SCHEMBL18709358 0.85 LMNA (0.67) RAB9AMAPTKMT2ANPC1
SCHEMBL20296959 0.85 LMNA (0.67) RAB9AMAPTKMT2ANPC1
SCHEMBL17329255 0.82 ATM (0.52) RAB9AMAPTKMT2ANPC1
SCHEMBL17329250 0.82 ATM (0.52) RAB9AMAPTKMT2ANPC1
SCHEMBL18687078 0.79 LMNA (0.66) RAB9AMAPTKMT2ANPC1
SCHEMBL18687079 0.79 LMNA (0.66) RAB9AMAPTKMT2ANPC1
SCHEMBL20296954 0.79 DDIT3 (0.56) DDIT3RAB9AMAPTKMT2A
SCHEMBL18709235 0.79 DDIT3 (0.56) DDIT3RAB9AMAPTKMT2A
SCHEMBL18709362 0.79 LMNA (0.48) RAB9AMAPTKMT2ANPC1

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-10071994-B2 N-sulfonyl homoserine lactone derivatives, preparation method and use thereof INSTITUTE OF PHARMACOLOGY AND TOXICOLOGY ACADEMY OF MILITARY MEDICAL SCIENCES P.L.A. CHINA (CN) 2018-09-11 US claimed
US-20180179193-A1 N-Sulfonyl Homoserine Lactone Derivatives, Preparation Method and Use Thereof INSTITUTE OF PHARMACOLOGY AND TOXICOLOGY ACADEMY OF MILITARY MEDICAL SCIENCES P.L.A. CHINA (CN) 2018-06-28 US claimed
US-10071994-B2 N-sulfonyl homoserine lactone derivatives, preparation method and use thereof INSTITUTE OF PHARMACOLOGY AND TOXICOLOGY ACADEMY OF MILITARY MEDICAL SCIENCES P.L.A. CHINA (CN) 2018-09-11 US disclosed
US-20180179193-A1 N-Sulfonyl Homoserine Lactone Derivatives, Preparation Method and Use Thereof INSTITUTE OF PHARMACOLOGY AND TOXICOLOGY ACADEMY OF MILITARY MEDICAL SCIENCES P.L.A. CHINA (CN) 2018-06-28 US disclosed
US-20180179193-A1 N-Sulfonyl Homoserine Lactone Derivatives, Preparation Method and Use Thereof INSTITUTE OF PHARMACOLOGY AND TOXICOLOGY ACADEMY OF MILITARY MEDICAL SCIENCES P.L.A. CHINA (CN) 2018-06-28 US disclosed
EP-3150594-A1 N-SULFONYL HOMOSERINE LACTONE DERIVATIVES, PREPARATION METHOD THEREFOR AND USE Institute of Pharmacology and Toxicology Academy of Military Medical Sciences P.L.A. China (CN) 2017-04-05 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 (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-20180179193-A1 N-Sulfonyl Homoserine Lactone Derivatives, Preparation Method and Use Thereof LSS, SOS1, STS DDIT3 3558/4885RAB9A 3200/4885MAPT 4807/4885
US-10071994-B2 N-sulfonyl homoserine lactone derivatives, preparation method and use thereof LSS, SOS1, STS DDIT3 3475/4885RAB9A 3180/4885MAPT 4813/4885

“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.