SCHEMBL3767355

SCHEMBL3767355

CC(C)(C)NS(=O)(=O)c1c(F)cccc1I

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 3/20 0.44
SMN1; SMN2 Q16637 2/20 0.44
KDM4E B2RXH2 1/20 0.44
MEN1 O00255 1/20 0.44
NPC1 O15118 1/20 0.44
LMNA P02545 1/20 0.44
HPGD P15428 1/20 0.44
RAB9A P51151 1/20 0.44
KMT2A Q03164 1/20 0.44
NSD2 O96028 2/20 0.41
ALDH1A1 P00352 2/20 0.40
CYP3A4 P08684 1/20 0.40
CYP2C9 P11712 1/20 0.40
MAPK1 P28482 1/20 0.40
ALOX5AP P20292 10/20 0.39
FEN1 P39748 10/20 0.39
PKM P14618 2/20 0.36
PARG Q86W56 1/20 0.36
PKLR P30613 1/20 0.36
NPSR1 Q6W5P4 1/20 0.35

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
SCHEMBL24429357 0.88 MAPT (0.50) MAPTSMN1; SMN2KDM4EMEN1NPC1
SCHEMBL3767141 0.78 SMN1; SMN2 (0.41) MAPTSMN1; SMN2KDM4EMEN1NPC1
SCHEMBL4058098 0.76 ALOX5AP (0.47) MAPTSMN1; SMN2KDM4EMEN1NPC1
SCHEMBL18077864 0.74 NSD2 (0.46) MAPTSMN1; SMN2KDM4EMEN1NPC1
SCHEMBL24429391 0.74 NSD2 (0.51) MAPTSMN1; SMN2KDM4EMEN1NPC1
SCHEMBL1111509 0.73 NSD2 (0.50) MAPTSMN1; SMN2KDM4EMEN1NPC1
SCHEMBL2893576 0.73 NSD2 (0.50) MAPTSMN1; SMN2KDM4EMEN1NPC1
SCHEMBL14837365 0.72 PKM (0.40) ALDH1A1PKMPKLR
SCHEMBL20560224 0.71 PKM (0.42) ALDH1A1PKMPKLR
SCHEMBL3771716 0.71 CA1 (0.43) PKMPKLR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7855166-B2 Sulfonylamino(thio)carbonyl compounds BAYER CROPSCIENCE GMBH (DE) 2010-12-21 US disclosed
US-20100317524-A1 Sulfonylureas BAYER CROPSCIENCE AG (DE) 2010-12-16 US disclosed
EP-1877386-A1 HERBICIDALLY ACTIVE PHENYLSULPHONYL-UREA Bayer CropScience AG (DE) 2008-01-16 EP disclosed
EP-1877380-A1 SULFONYLAMINO(THIO)CARBONYL COMPOUNDS IN THE FORM OF HERBICIDES OR PLANT GROWTH REGULATORS BAYER CROPSCIENCE AG (DE) 2008-01-16 EP disclosed
US-20060264329-A1 Sulfonylureas BAYER CROPSCIENCE GMBH (DE) 2006-11-23 US disclosed
US-20060258536-A1 Sulfonylamino(thio)carbonyl compounds BAYER CROPSCIENCE GMBH (DE) 2006-11-16 US disclosed
EP-1717228-A1 Sulfonylamino(thio)carbonylderivatives as herbicides or plant growth regulators Bayer CropScience GmbH (DE) 2006-11-02 EP disclosed
EP-1717232-A1 Phenylsulfonylureas with herbicidal activity Bayer CropScience GmbH (DE) 2006-11-02 EP disclosed
WO-2006114221-A1 SULFONYLAMINO(THIO)CARBONYL COMPOUNDS IN THE FORM OF HERBICIDES OR PLANT GROWTH REGULATORS BAYER CROPSCIENCE AG (DE) 2006-11-02 WO disclosed
WO-2006114220-A1 HERBICIDALLY ACTIVE PHENYLSULPHONYL-UREA BAYER CROPSCIENCE AG (DE) 2006-11-02 WO 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 (3 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-20100317524-A1 Sulfonylureas IAPP, SLC5A2, SLC5A1 MAPT 4258/4885SMN1; SMN2 1174/4885KDM4E 2871/4885
US-20060258536-A1 Sulfonylamino(thio)carbonyl compounds TST, CBR3, MYB MAPT 3054/4885SMN1; SMN2 4458/4885KDM4E 1546/4885
US-20060264329-A1 Sulfonylureas INSR, FFAR3, GPR119 MAPT 4837/4885SMN1; SMN2 952/4885KDM4E 3101/4885

“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.