SCHEMBL17329231

SCHEMBL17329231

O=C(Nc1ccc(S(=O)(=O)NC2CCOC2=O)cc1)c1ccc(Cl)cc1

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 2/20 0.52
KMT2A Q03164 2/20 0.52
NPC1 O15118 2/20 0.52
PRMT1 Q99873 2/20 0.49
MAPT P10636 2/20 0.49
HSD17B10 Q99714 1/20 0.49
MAOB P27338 1/20 0.46
RAB9A P51151 1/20 0.46
KCNA5 P22460 1/20 0.46
LMNA P02545 2/20 0.45
TP53 P04637 1/20 0.45
NAMPT P43490 1/20 0.45
HTT P42858 1/20 0.45
SMN1; SMN2 Q16637 1/20 0.45
FLT1 P17948 1/20 0.45
FLT4 P35916 1/20 0.45
KDR P35968 1/20 0.45
CA12 O43570 1/20 0.45
CA1 P00915 1/20 0.45
CA9 Q16790 1/20 0.45

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
SCHEMBL17329230 1.00 MEN1 (0.52) MEN1KMT2ANPC1PRMT1MAPT
SCHEMBL17329200 0.89 MEN1 (0.56) MEN1KMT2ANPC1MAPTHSD17B10
SCHEMBL17329223 0.89 MEN1 (0.47) MEN1KMT2ANPC1MAPTHSD17B10
SCHEMBL17329259 0.89 MEN1 (0.56) MEN1KMT2ANPC1MAOBRAB9A
SCHEMBL17329224 0.89 MEN1 (0.47) MEN1KMT2ANPC1MAPTHSD17B10
SCHEMBL17329258 0.89 MEN1 (0.56) MEN1KMT2ANPC1MAOBRAB9A
SCHEMBL17329201 0.89 MEN1 (0.56) MEN1KMT2ANPC1MAPTHSD17B10
SCHEMBL17329184 0.89 PRMT1 (0.52) MEN1KMT2APRMT1LMNACA12
SCHEMBL17329183 0.89 PRMT1 (0.52) MEN1KMT2APRMT1LMNACA12
SCHEMBL17329208 0.88 KMT2A (0.46) MEN1KMT2ANPC1MAPTHSD17B10

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-9630939-B2 Derivative of homoserine lactone, and preparation method and use thereof INSTITUTE OF PHARMACOLOGY AND TOXICOLOGY ACADEMY OF MILITARY MEDICAL SCIENCES P.L.A. CHINA (CN) 2017-04-25 US claimed
US-20150368217-A1 Derivative of Homoserine Lactone, and Preparation Method and Use Thereof INSTITUTE OF PHARMACOLOGY AND TOXICOLOGY ACADEMY OF MILITARY MEDICAL SCIENCES P.L.A. CHINA (CN) 2015-12-24 US claimed
EP-2955174-A1 DERIVATIVE OF HOMOSERINE LACTONE, AND PREPARATION METHOD AND USE THEREOF Institute of Pharmacology and Toxicology Academy of Military Medical Sciences P.L.A. China (CN) 2015-12-16 EP claimed
US-9630939-B2 Derivative of homoserine lactone, and preparation method and use thereof INSTITUTE OF PHARMACOLOGY AND TOXICOLOGY ACADEMY OF MILITARY MEDICAL SCIENCES P.L.A. CHINA (CN) 2017-04-25 US disclosed
US-20150368217-A1 Derivative of Homoserine Lactone, and Preparation Method and Use Thereof INSTITUTE OF PHARMACOLOGY AND TOXICOLOGY ACADEMY OF MILITARY MEDICAL SCIENCES P.L.A. CHINA (CN) 2015-12-24 US disclosed
EP-2955174-A1 DERIVATIVE OF HOMOSERINE LACTONE, AND PREPARATION METHOD AND USE THEREOF Institute of Pharmacology and Toxicology Academy of Military Medical Sciences P.L.A. China (CN) 2015-12-16 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-20150368217-A1 Derivative of Homoserine Lactone, and Preparation Method and Use Thereof LSS, HES1, SOS1 MEN1 589/4885KMT2A 3880/4885NPC1 3828/4885

“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.