SCHEMBL4487513

SCHEMBL4487513

O=S(=O)(NCc1cccc2ccccc12)c1cccc2c(O)cccc12

nearest known ligand 0.60

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA2 P00918 2/20 0.60
HCRTR1 O43613 1/20 0.48
CDK2 P24941 1/20 0.47
NPY1R P25929 1/20 0.47
NPY5R Q15761 1/20 0.47
NSD2 O96028 2/20 0.47
KDM4E B2RXH2 2/20 0.46
KCNA5 P22460 2/20 0.46
SCN1A P35498 2/20 0.46
SCN2A Q99250 2/20 0.46
SCN3A Q9NY46 2/20 0.46
ALDH1A1 P00352 2/20 0.46
CYP1A2 P05177 2/20 0.46
CYP3A4 P08684 1/20 0.46
CYP2C9 P11712 1/20 0.46
CYP2C19 P33261 1/20 0.46
HSD17B10 Q99714 1/20 0.46
MCL1 Q07820 1/20 0.44
HTT P42858 1/20 0.44
PFKFB3 Q16875 1/20 0.44

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
SCHEMBL4492415 0.85 ALDH1A1 (0.55) CA2HCRTR1CDK2NSD2KDM4E
SCHEMBL4449107 0.83 NSD2 (0.68) CA2NPY5RNSD2KDM4ESCN1A
Hydrochloric Acid SCHEMBL4449077 0.82 NSD2 (0.69) CA2NSD2KDM4ESCN1ASCN2A
SCHEMBL4483058 0.82 NPY1R (0.49) CA2CDK2NPY1RNPY5RNSD2
SCHEMBL4480649 0.82 MEN1 (0.53) NSD2KDM4EALDH1A1HTT
SCHEMBL4483905 0.81 NSD2 (0.69) CDK2NSD2KDM4EALDH1A1MCL1
SCHEMBL4478162 0.80 CA2 (0.56) CA2ALDH1A1CYP1A2CYP3A4CYP2C9
SCHEMBL4448161 0.80 NPY5R (0.50) CA2NPY5RNSD2KCNA5
SCHEMBL4489171 0.77 LMNA (0.51) CA2NSD2ALDH1A1CA12
SCHEMBL4488539 0.76 MCL1 (0.49) CDK2KDM4EALDH1A1CYP1A2CYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7598418-B2 Naphthalene-1-(sulfonamide or carboxamide) derivatives; e.g. N-Benzyl-5-{[(4-methylphenyl)sulfonyl]oxy}naphthalene-1-sulfonamide; protein kinase inhibitors sensitize cancer cells to radiotherapy or anticancer agents; side effect reduction INSTITUTE OF MEDICINAL MOLECULAR DESIGN, INC. (JP) 2009-10-06 US claimed
US-20050215645-A1 Amide derivatives INSTITUTE OF MEDICINAL MOLECULAR DESIGN. INC. (JP) 2005-09-29 US claimed
US-7598418-B2 Naphthalene-1-(sulfonamide or carboxamide) derivatives; e.g. N-Benzyl-5-{[(4-methylphenyl)sulfonyl]oxy}naphthalene-1-sulfonamide; protein kinase inhibitors sensitize cancer cells to radiotherapy or anticancer agents; side effect reduction INSTITUTE OF MEDICINAL MOLECULAR DESIGN, INC. (JP) 2009-10-06 US disclosed
US-20050215645-A1 Amide derivatives INSTITUTE OF MEDICINAL MOLECULAR DESIGN. INC. (JP) 2005-09-29 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-20050215645-A1 Amide derivatives OGG1, HDAC1, BCL2A1 CA2 926/4885HCRTR1 1310/4885CDK2 802/4885

“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.