SCHEMBL8508293

SCHEMBL8508293

COc1ccc(S(=O)(=O)N2CCCCC2)cc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HTT P42858 1/20 1.00
ALDH1A1 P00352 9/20 0.87
KDM4E B2RXH2 3/20 0.87
PKM P14618 2/20 0.83
RAB9A P51151 2/20 0.83
NPC1 O15118 1/20 0.83
PKLR P30613 1/20 0.83
L3MBTL1 Q9Y468 2/20 0.74
POLB P06746 1/20 0.74
SMN1; SMN2 Q16637 2/20 0.73
MAPT P10636 2/20 0.73
CYP2D6 P10635 1/20 0.73
CYP2C19 P33261 1/20 0.73
KMT2A Q03164 3/20 0.71
USP2 O75604 2/20 0.71
MEN1 O00255 2/20 0.71
GAA P10253 3/20 0.69
TSHR P16473 2/20 0.69
NPSR1 Q6W5P4 1/20 0.69
LMNA P02545 1/20 0.69

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
SCHEMBL4555472 1.00 HTT (1.00) HTTALDH1A1KDM4EPKMRAB9A
SCHEMBL1044915 0.98 HTT (0.96) HTTALDH1A1KDM4EPKMRAB9A
SCHEMBL1722721 0.91 PKM (1.00) HTTALDH1A1KDM4EPKMRAB9A
SCHEMBL31315853 0.91 PKM (1.00) HTTALDH1A1KDM4EPKMRAB9A
SCHEMBL1472052 0.85 USP2 (0.77) HTTALDH1A1KDM4EPKMRAB9A
SCHEMBL16281071 0.84 PKM (0.86) HTTALDH1A1KDM4EPKMRAB9A
SCHEMBL12793019 0.84 ALDH1A1 (1.00) HTTALDH1A1KDM4EPKMRAB9A
SCHEMBL17007474 0.83 ALDH1A1 (0.97) HTTALDH1A1KDM4EPKMRAB9A
SCHEMBL16502896 0.83 ALDH1A1 (0.91) HTTALDH1A1KDM4EPKMRAB9A
SCHEMBL1352340 0.83 PKM (0.77) HTTALDH1A1KDM4EPKMRAB9A

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
CN-109020924-B Method for synthesizing benzene sulfonamide compound from benzene sulfonyl chloride compound and secondary amine through metal-free catalysis 湖南农业大学 2022-05-13 CN disclosed
WO-2020028482-A1 SMALL MOLECULES THAT SENSITIZE HIV-1 INFECTED CELLS TO ANTIBODY DEPENDENT CELLULAR CYTOTOXICITY THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA (US) 2020-02-06 WO disclosed
US-20080306069-A1 Pyrazole Derivatives for the Inhibition of CDK'S and GSK'S ASTEX THERAPEUTICS LIMITED (UK) 2008-12-11 US disclosed
US-20080306069-A1 Pyrazole Derivatives for the Inhibition of CDK'S and GSK'S ASTEX THERAPEUTICS LIMITED (UK) 2008-12-11 US disclosed
EP-0923547-A1 BIDENTATE METALLOPROTEASE INHIBITORS THE PROCTER & GAMBLE COMPANY (US) 1999-06-23 EP disclosed
WO-1998008814-A1 BIDENTATE METALLOPROTEASE INHIBITORS THE PROCTER & GAMBLE COMPANY (US) 1998-03-05 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 (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-20080306069-A1 Pyrazole Derivatives for the Inhibition of CDK'S and GSK'S GSK3A, CDK11A, CDK1 HTT 4489/4885ALDH1A1 1576/4885KDM4E 1457/4885

“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.