SCHEMBL7124469

SCHEMBL7124469

CC(C)(C)C(NS(=O)(=O)c1ccc(C(N)=O)cc1)(C(N)=O)c1ccccc1

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
POLB P06746 2/20 0.46
MAPT P10636 3/20 0.43
KAT6A Q92794 1/20 0.42
NR3C2 P08235 1/20 0.42
CA2 P00918 2/20 0.41
KMT2A Q03164 2/20 0.41
CA12 O43570 2/20 0.40
CA9 Q16790 2/20 0.40
CYP2C19 P33261 2/20 0.40
TMPRSS6 Q8IU80 2/20 0.40
CYP3A4 P08684 1/20 0.40
PARP1 P09874 1/20 0.40
TSHR P16473 1/20 0.40
RECQL P46063 1/20 0.40
BLM P54132 1/20 0.40
PMP22 Q01453 1/20 0.40
HSD17B10 Q99714 1/20 0.40
TDP1 Q9NUW8 1/20 0.40
L3MBTL1 Q9Y468 1/20 0.40
CA1 P00915 1/20 0.39

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
SCHEMBL5458574 0.78 CA2 (0.53) POLBMAPTKAT6ACA2KMT2A
SCHEMBL7127023 0.75 GHSR (0.42) POLBMAPTKAT6ACA2KMT2A
SCHEMBL5452240 0.70 TMPRSS6 (0.73) POLBCA2KMT2ACA12CA9
SCHEMBL7118423 0.69 LMNA (0.44) POLBCA2KMT2ACYP2C19CYP3A4
SCHEMBL1870821 0.69 CA2 (0.59) POLBKAT6ANR3C2CA2CA12
SCHEMBL376340 0.69 MEN1 (0.73) POLBMAPTKAT6ACA2KMT2A
SCHEMBL7895365 0.69 MEN1 (0.54) MAPTCA2KMT2ACA12CA9
Hydrochloric Acid SCHEMBL5344895 0.68 CA2 (0.57) POLBKAT6ANR3C2CA2CA12
SCHEMBL28400732 0.68 ALDH1A1 (0.50) MAPTNR3C2CA2CYP2C19TDP1
SCHEMBL10934017 0.68 PLA2G10 (0.43) POLBMAPTCA2KMT2ACA12

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 POLB 1804/4885MAPT 1707/4885KAT6A 412/4885

“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.