SCHEMBL5751524

SCHEMBL5751524

O=c1[nH]cc(S(=O)(=O)Cl)c(=O)[nH]1

nearest known ligand 0.45

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
▸ DPYD Q12882 5/20 0.45
▸ MAPT P10636 3/20 0.45
▸ ALDH1A1 P00352 2/20 0.45
▸ LMNA P02545 2/20 0.45
▸ GAA P10253 2/20 0.45
▸ ATAD2 Q6PL18 1/20 0.45
▸ CYP19A1 P11511 1/20 0.45
▸ TSHR P16473 1/20 0.45
▸ THPO P40225 1/20 0.45
▸ MTOR P42345 1/20 0.45
▸ HTT P42858 1/20 0.45
▸ HBB P68871 1/20 0.45
▸ PMP22 Q01453 1/20 0.45
▸ SMN1; SMN2 Q16637 1/20 0.45
▸ KDM4C Q9H3R0 1/20 0.40
▸ TYMS P04818 2/20 0.34

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
SCHEMBL27623146 0.78 GAA (0.50) DPYDMAPTALDH1A1LMNAGAA
SCHEMBL6684769 0.78 ATAD2 (0.50) DPYDMAPTALDH1A1LMNAGAA
Hydrochloric Acid SCHEMBL28250779 0.77 GAA (0.48) DPYDMAPTALDH1A1LMNAGAA
SCHEMBL67366 0.67 — —
SCHEMBL30727452 0.67 PARP1 (0.50) ALDH1A1LMNAPMP22SMN1; SMN2
SCHEMBL3282669 0.67 PARP1 (0.50) ALDH1A1LMNAPMP22SMN1; SMN2
SCHEMBL5801644 0.66 ALDH1A1 (0.64) DPYDMAPTALDH1A1LMNAGAA
Water SCHEMBL27711509 0.65 DPYD (0.50) DPYDMAPTALDH1A1LMNAGAA
SCHEMBL6573722 0.64 — —
SCHEMBL21930973 0.64 DAO (0.50) ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109705045-B Pyrimidine antitumor compound and preparation method and application thereof 中国医科大学 2020-07-14 — — CN claimed
CN-108774218-B Pyrimidine antitumor compound with 1,3, 4-oxadiazole structure and preparation method and application thereof 中国医科大学 2020-04-21 — — CN claimed
CN-108794408-B Pyrimidine phenylurea anti-tumor compound and preparation method and application thereof 中国医科大学 2020-04-21 — — CN claimed
CN-109705045-A Pyrimidine anti-tumor compounds and its preparation method and application 中国医科大学 2019-05-03 — — CN claimed
CN-108794408-A Pyrimidine phenylurea anti-tumor compounds and its preparation method and application 中国医科大学 2018-11-13 — — CN claimed
CN-108774218-A The pyrimidine anti-tumor compounds and its preparation method and application of 1,3,4- oxadiazoles structures 中国医科大学 2018-11-09 — — CN claimed
US-20250115687-A1 PRODUCTION METHOD FOR SOLID CATALYST COMPONENT FOR POLYMERIZING OLEFINS, AND CATALYST FOR POLYMERIZAING OLEFINS FORMOSA PLASTICS CORP USA (US) 2025-04-10 — — US disclosed
WO-2025075722-A1 PRODUCTION METHOD FOR SOLID CATALYST COMPONENT FOR POLYMERIZING OLEFINS, AND CATALYST FOR POLYMERIZAING OLEFINS FORMOSA PLASTICS CORPORATION, U.S.A. (US) 2025-04-10 — — WO disclosed
CN-109705045-B Pyrimidine antitumor compound and preparation method and application thereof 中国医科大学 2020-07-14 — — CN disclosed
CN-108774218-B Pyrimidine antitumor compound with 1,3, 4-oxadiazole structure and preparation method and application thereof 中国医科大学 2020-04-21 — — CN disclosed
CN-108794408-B Pyrimidine phenylurea anti-tumor compound and preparation method and application thereof 中国医科大学 2020-04-21 — — CN disclosed
CN-109705045-A Pyrimidine anti-tumor compounds and its preparation method and application 中国医科大学 2019-05-03 — — CN disclosed
CN-108794408-A Pyrimidine phenylurea anti-tumor compounds and its preparation method and application 中国医科大学 2018-11-13 — — CN disclosed
WO-2003079986-A2 URACIL DERIVATIVES AS INHIBITORS OF TNF-ALPHA CONVERTING ENZYME (TACE) AND MATRIX METALLOPROTEINASES BRISTOL-MYERS SQUIBB COMPANY (US) 2003-10-02 — — WO disclosed
WO-2003079986-A2 URACIL DERIVATIVES AS INHIBITORS OF TNF-ALPHA CONVERTING ENZYME (TACE) AND MATRIX METALLOPROTEINASES BRISTOL-MYERS SQUIBB COMPANY (US) 2003-10-02 — — WO disclosed
EP-1299361-A1 PYRAZOLE DERIVATIVES Pfizer Limited (GB) 2003-04-09 — — EP disclosed
WO-2002004424-A9 PYRAZOLE DERIVATIVES PFIZER LTD (GB) 2002-12-12 — — WO disclosed
US-20020032184-A1 Pyrazole derivatives PFIZER INC. 2002-03-14 — — US disclosed
WO-2002004424-A1 PYRAZOLE DERIVATIVES PFIZER LIMITED (GB) 2002-01-17 — — WO disclosed
US-3948901-A Bis (2,4-dioxotetrahydropyrimidinyl-5-sulphonoamido) diphenylsulphoner REZNIK VLADIMIR SAVICH 1976-04-06 — — 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-20020032184-A1 Pyrazole derivatives POLRMT, TPMT, CYP3A43 DPYD 6/4885MAPT 788/4885ALDH1A1 228/4885

“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.

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