SCHEMBL3377958

SCHEMBL3377958

CS(=O)(=O)N1CCC(C(N)=O)CC1

nearest known ligand 0.61

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
TP53 P04637 1/20 0.61
SMN1; SMN2 Q16637 3/20 0.54
TSHR P16473 1/20 0.54
POLB P06746 2/20 0.53
ALDH1A1 P00352 3/20 0.50
NPSR1 Q6W5P4 3/20 0.50
L3MBTL1 Q9Y468 2/20 0.49
HTT P42858 1/20 0.49
MAPT P10636 1/20 0.49
CYP2C19 P33261 1/20 0.47
MEN1 O00255 1/20 0.46
KMT2A Q03164 1/20 0.46
GAA P10253 1/20 0.46

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
SCHEMBL6968129 0.88 TP53 (0.53) TP53SMN1; SMN2TSHRPOLBALDH1A1
Hydrochloric Acid SCHEMBL17510088 0.86 TP53 (0.51) TP53SMN1; SMN2TSHRPOLBALDH1A1
SCHEMBL29851226 0.83 POLB (0.51) TP53SMN1; SMN2POLBALDH1A1NPSR1
SCHEMBL22749233 0.82 SMN1; SMN2 (0.60) TP53SMN1; SMN2TSHRPOLBALDH1A1
SCHEMBL18519633 0.81 TP53 (0.54) TP53SMN1; SMN2TSHRPOLBALDH1A1
SCHEMBL12437005 0.81 TP53 (0.63) TP53SMN1; SMN2TSHRPOLBALDH1A1
SCHEMBL607186 0.81 TP53 (0.63) TP53SMN1; SMN2TSHRPOLBALDH1A1
SCHEMBL4682503 0.79 TP53 (0.61) TP53SMN1; SMN2TSHRPOLBALDH1A1
SCHEMBL13411078 0.79 EPHX2 (0.53) TP53SMN1; SMN2TSHRPOLBALDH1A1
SCHEMBL5398339 0.79 TP53 (0.51) TP53SMN1; SMN2TSHRPOLBALDH1A1

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 52 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119855813-A Pyridazinone-derived compounds for modulating MYC and for medical use 遗传智力公司 2025-04-18 CN claimed
EP-3980410-A1 N-(4-(5-CHLOROPYRIDIN-3-YL)PHENYL)-2-(2-(CYCLOPROPANESULFONAMIDO)PYRIMIDIN-4-YL) BUTANAMIDE DERIVATIVES AND RELATED COMPOUNDS AS HUMAN CTPS1 INHIBITORS FOR THE TREATMENT OF PROLIFERATIVE DISEASES Step Pharma S.A.S. (FR) 2022-04-13 EP claimed
WO-2020245665-A1 N-(4-(5-CHLOROPYRIDIN-3-YL)PHENYL)-2-(2-(CYCLOPROPANESULFONAMIDO)PYRIMIDIN-4-YL) BUTANAMIDE DERIVATIVES AND RELATED COMPOUNDS AS HUMAN CTPS1 INHIBITORS FOR THE TREATMENT OF PROLIFERATIVE DISEASES STEP PHARMA S.A.S. (FR) 2020-12-10 WO claimed
EP-3145912-A1 BENZENE SULFONAMIDE DERIVATIVES AND THEIR USE AS RORC MODULATORS F. Hoffmann-La Roche AG (CH) 2017-03-29 EP claimed
WO-2015177325-A1 BENZENE SULFONAMIDE DERIVATIVES AND THEIR USE AS RORC MODULATORS F. HOFFMANN-LA ROCHE AG (CH) 2015-11-26 WO claimed
US-8288431-B2 Substituted spiroindolinones HOFFMANN-LA ROCHE INC. (US) 2012-10-16 US claimed
EP-2134703-A1 AMIDE DERIVATIVES AS CALCIUM CHANNEL BLOCKERS Neuromed Pharmaceuticals, Ltd. (CA) 2009-12-23 EP claimed
WO-2008110008-A1 AMIDE DERIVATIVES AS CALCIUM CHANNEL BLOCKERS NEUROMED PHARMACEUTICALS LTD. (CA) 2008-09-18 WO claimed
WO-2006130426-A2 MODULATORS OF CCR-5 ACTIVITY KEMIA, INC. (US) 2006-12-07 WO claimed
US-12637440-B2 Amide derivative useful as diacylglycerol acyltransferase 2 inhibitor, and use thereof LG CHEM, LTD. (KR) 2026-05-26 US disclosed
US-12319683-B2 Azabenzimidazole compounds and pharmaceutical NIPPON SHINYAKU CO., LTD. (JP) 2025-06-03 US disclosed
WO-2025021182-A1 CYP11A1 INHIBITORS ACERAND THERAPEUTICS (HONG KONG) LIMITED (CN) 2025-01-30 WO disclosed
EP-4486347-A1 COMBINATIONS OF CTPS1 AND BCL2 INHIBITORS FOR CANCER Step Pharma S.A.S. (FR) 2025-01-08 EP disclosed
CN-114901653-B Novel amide derivatives useful as diacylglycerol acyltransferase 2 inhibitors and uses thereof 株式会社LG化学 2024-11-22 CN disclosed
WO-2008133344-A2 PIPERIDINE DERIVATIVE AND USE THEREOF TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2008-11-06 WO disclosed
EP-1878725-A2 Pyrimidine derivatives and their use as CB2 modulators GLAXO GROUP LIMITED (GB) 2008-01-16 EP disclosed
US-20060293354-A1 Pyrimidine derivatives and their use as CB2 modulators GLAXO GROUP LIMITED (GB) 2006-12-28 US disclosed
WO-2006130426-A2 MODULATORS OF CCR-5 ACTIVITY KEMIA, INC. (US) 2006-12-07 WO disclosed
EP-1220842-A1 CYCLIC AMINE COMPOUNDS AS CCR5 ANTAGONISTS Takeda Chemical Industries, Ltd. (JP) 2002-07-10 EP disclosed
WO-2001025200-A1 CYCLIC AMINE COMPOUNDS AS CCR5 ANTAGONISTS TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 2001-04-12 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-20060293354-A1 Pyrimidine derivatives and their use as CB2 modulators CNR2, CNR1, P2RX3 TP53 3563/4885SMN1; SMN2 3473/4885TSHR 2969/4885
US-12319683-B2 Azabenzimidazole compounds and pharmaceutical PAM, CHRM3, AZI2 TP53 1770/4885SMN1; SMN2 1008/4885TSHR 3490/4885
US-12637440-B2 Amide derivative useful as diacylglycerol acyltransferase 2 inhibitor, and use thereof DGAT2, DGAT1, DLAT TP53 4684/4885SMN1; SMN2 4700/4885TSHR 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.