SCHEMBL7130244

SCHEMBL7130244

NC(=O)c1ccc(S(=O)(=O)NC(CCc2ccccc2)(C(N)=O)C2CCCCC2)cc1

nearest known ligand 0.41

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HTT P42858 2/20 0.41
ALDH1A1 P00352 1/20 0.41
CYP1A2 P05177 1/20 0.41
CYP3A4 P08684 1/20 0.41
CYP2D6 P10635 1/20 0.41
CYP2C9 P11712 1/20 0.41
CYP2C19 P33261 1/20 0.41
NPSR1 Q6W5P4 1/20 0.41
POLB P06746 1/20 0.41
PPARG P37231 1/20 0.40
KMT2A Q03164 1/20 0.40
PRMT1 Q99873 1/20 0.39
USP30 Q70CQ3 4/20 0.39
CRHBP P24387 1/20 0.38
CRHR2 Q13324 1/20 0.38
OPRM1 P35372 1/20 0.38
OPRD1 P41143 1/20 0.38
PLA2G10 O15496 1/20 0.37
PLA2G2A P14555 1/20 0.37
MCL1 Q07820 1/20 0.37

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
SCHEMBL7116603 0.77 PRMT1 (0.43) ALDH1A1POLBPRMT1OPRM1OPRD1
SCHEMBL7127023 0.76 GHSR (0.42) ALDH1A1NPSR1POLBKMT2APRMT1
SCHEMBL7118423 0.73 LMNA (0.44) ALDH1A1CYP3A4CYP2D6CYP2C9CYP2C19
SCHEMBL7130241 0.70 PLAU (0.54) HTTALDH1A1CYP1A2CYP3A4CYP2D6
SCHEMBL4278250 0.68 L3MBTL1 (0.45) ALDH1A1CYP2C19KMT2ATAAR1TSHR
SCHEMBL5449745 0.67 PRMT1 (0.68) HTTALDH1A1CYP1A2CYP3A4CYP2D6
SCHEMBL27915795 0.67 PARP10 (0.54) POLBKMT2APRMT1PLA2G10PLA2G2A
SCHEMBL7124462 0.66 GAA (0.45) ALDH1A1CYP1A2CYP2C9CYP2C19NPSR1
SCHEMBL7116706 0.65 PLAU (0.59) ALDH1A1CYP1A2CYP2C9CYP2C19PLAU
SCHEMBL7127820 0.65 GHSR (0.43) ALDH1A1NPSR1KMT2APRMT1TSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6583318-B2 Carrying out a four component condensation reaction between components consisting of a sulfonamide, an aldehyde or ketone, an isocyanide and a carboxylic acid, and one of such components being attached to a solid support ADVANCED SYNTECH, LLC 2003-06-24 US disclosed
US-20030013910-A1 Method for synthesis of alpha-sulfonamido amide, carboxylic acid and hydroxamic acid derivatives ADVANCED SYNTECH LLC 2003-01-16 US 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-20030013910-A1 Method for synthesis of alpha-sulfonamido amide, carboxylic acid and hydroxamic acid derivatives ASPH, COASY, HAAO HTT 380/4885ALDH1A1 391/4885CYP1A2 2348/4885

“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.