SCHEMBL2967442

SCHEMBL2967442

O=[N+]([O-])c1ccc(S(=O)(=O)OCC2CO2)cc1

nearest known ligand 0.72

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PRMT5 O14744 1/20 0.72
WDR77 Q9BQA1 1/20 0.72
PKM P14618 2/20 0.46
ALDH1A1 P00352 2/20 0.46
LMNA P02545 1/20 0.46
GAA P10253 1/20 0.46
CA2 P00918 8/20 0.43
CA1 P00915 7/20 0.43
CA9 Q16790 7/20 0.43
CA12 O43570 6/20 0.43
CA14 Q9ULX7 5/20 0.43
CA7 P43166 4/20 0.43
CA3 P07451 3/20 0.43
CA4 P22748 3/20 0.43
CA6 P23280 3/20 0.43
CA5A P35218 3/20 0.43
CA13 Q8N1Q1 3/20 0.43
CA5B Q9Y2D0 3/20 0.43
MMP2 P08253 2/20 0.40
MMP1 P03956 1/20 0.40

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
SCHEMBL9645456 1.00 PRMT5 (0.72) PRMT5WDR77PKMALDH1A1LMNA
SCHEMBL1164097 1.00 PRMT5 (0.72) PRMT5WDR77PKMALDH1A1LMNA
SCHEMBL30301224 0.84 PRMT5 (1.00) PRMT5WDR77ALDH1A1LMNAGAA
SCHEMBL336605 0.84 PRMT5 (1.00) PRMT5WDR77ALDH1A1LMNAGAA
SCHEMBL336603 0.84 PRMT5 (1.00) PRMT5WDR77ALDH1A1LMNAGAA
SCHEMBL29481767 0.84 PRMT5 (1.00) PRMT5WDR77ALDH1A1LMNAGAA
SCHEMBL449928 0.84 PRMT5 (1.00) PRMT5WDR77ALDH1A1LMNAGAA
SCHEMBL29476299 0.84 PRMT5 (1.00) PRMT5WDR77ALDH1A1LMNAGAA
SCHEMBL9303799 0.83 PRMT5 (0.53) PRMT5WDR77PKMALDH1A1CA2
SCHEMBL7470093 0.83 PRMT5 (0.67) PRMT5WDR77PKMALDH1A1LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119708491-A Polydisulfide polymer material containing hydroxy ester group and preparation method thereof 衢州化工新材料创新研究院 2025-03-28 CN claimed
WO-2014140220-A1 PROCESS FOR THE PREPARATION OF (2,3-DIHYDRO-BENZO[B][1,4]DIOXIN-2-YL) METHANOL DERIVATIVES JANSSEN PHARMACEUTICA, N.V. (BE) 2014-09-18 WO claimed
CN-119708491-A Polydisulfide polymer material containing hydroxy ester group and preparation method thereof 衢州化工新材料创新研究院 2025-03-28 CN disclosed
CN-117242073-A PRMT5 inhibitors and uses thereof 海思科医药集团股份有限公司 2023-12-15 CN disclosed
WO-2022206964-A1 PRMT5 INHIBITOR AND USE THEREOF 海思科医药集团股份有限公司 2022-10-06 WO disclosed
CN-107226797-B A kind of chipal compounds 2, the preparation method of 2- dimethyl -3- (ethylene oxide -2- base) methyl propionate 沈阳金久奇科技有限公司 2019-05-17 CN disclosed
WO-2016071382-A1 SYNTHESIS OF PI3K INHIBITOR AND SALTS THEREOF BAYER PHARMA AKTIENGESELLSCHAFT (DE) 2016-05-12 WO disclosed
EP-1973917-B1 PROTEIN KINASE INHIBITORS ABBVIE INC (US) 2015-06-10 EP disclosed
US-8552188-B2 Epoxy compound and method for manufacturing the same OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2013-10-08 US disclosed
US-20130072683-A1 EPOXY COMPOUND AND METHOD FOR MANUFACTURING THE SAME OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2013-03-21 US disclosed
US-8344148-B2 Epoxy compound and method for manufacturing the same OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2013-01-01 US disclosed
US-6087512-A Process for preparation of glycidyl ether DAISO CO., LTD. (JP) 2000-07-11 US disclosed
US-6057476-A Process for the preparation of 3-amino-2-hydroxy-1-propyl ethers DAISO CO., LTD. (JP) 2000-05-02 US disclosed
EP-0930291-A1 PROCESS FOR THE PREPARATION OF 3-AMINO-2-HYDROXY-1-PROPYL ETHERS DAISO CO., LTD. (JP) 1999-07-21 EP disclosed
EP-0930307-A1 PROCESS FOR THE PREPARATION OF GLYCIDYL ETHERS DAISO CO., LTD. (JP) 1999-07-21 EP disclosed
CN-1160714-A Process for stereoselective preparation of hetero-bicyclic alcohol enantiomer DUPHAR INT RES (NL) 1997-10-01 CN disclosed
EP-0786459-A1 Process for the preparation of a hetero-bicyclic alcohol enantiomer DUPHAR INTERNATIONAL RESEARCH B.V (NL) 1997-07-30 EP disclosed
EP-0609025-B1 Process for producing optically active epoxy alcohol derivatives ARCO CHEM TECH (US) 1996-04-17 EP disclosed
EP-0609025-A1 Process for producing optically active epoxy alcohol derivatives ARCO Chemical Technology, L.P. (US) 1994-08-03 EP disclosed
US-4877892-A Chiral glycidyl azides as synthetic intermediates to optically active compounds E. I. DU PONT DE NEMOURS AND COMPANY (US) 1989-10-31 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-20130072683-A1 EPOXY COMPOUND AND METHOD FOR MANUFACTURING THE SAME SQLE, CYP2E1, CYP1A1 PRMT5 393/4885WDR77 343/4885PKM 1495/4885

“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.