SCHEMBL9645456

SCHEMBL9645456

O=[N+]([O-])c1ccc(S(=O)(=O)OC[C@H]2CO2)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
SCHEMBL1164097 1.00 PRMT5 (0.72) PRMT5WDR77PKMALDH1A1LMNA
SCHEMBL2967442 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 20 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-106582334-A Composite reverse osmosis membrane and preparation method and application thereof 中国石油化工股份有限公司 2017-04-26 CN claimed
US-20140275576-A1 PROCESS FOR THE PREPARATION OF (2,3-DIHYDRO-BENZO[B][1,4]DIOXIN-2-YL) METHANOL DERIVATIVES JANSSEN PHARMACEUTICA NV (BE) 2014-09-18 US claimed
US-12303474-B2 S-enantiomerically enriched compositions of beta blockers for treating amyotrophic lateral sclerosis ACTIMED THERAPEUTICS LIMITED (GB) 2025-05-20 US disclosed
US-20240325322-A1 S-ENANTIOMERICALLY ENRICHED COMPOSITIONS OF BETA BLOCKERS FOR TREATING AMYOTROPHIC LATERAL SCLEROSIS ACTIMED THERAPEUTICS LTD (GB) 2024-10-03 US disclosed
US-11938102-B2 S-enantiomerically enriched compositions of beta blockers for treating amyotrophic lateral sclerosis ACTIMED THERAPEUTICS LIMITED (GB) 2024-03-26 US disclosed
US-20230416263-A1 CARM1 INHIBITORS AND USES THEREOF Epizyme, Inc. (US) 2023-12-28 US 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
US-11834455-B2 Carm1 inhibitors and uses thereof Epizyme, Inc. (US) 2023-12-05 US disclosed
US-20230279020-A9 CARM1 INHIBITORS AND USES THEREOF Epizyme, Inc. (US) 2023-09-07 US 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
US-11433036-B2 Oxprenolol compositions for treating cancer ACTIMED THERAPEUTICS LIMITED (GB) 2022-09-06 US disclosed
CN-106582334-A Composite reverse osmosis membrane and preparation method and application thereof 中国石油化工股份有限公司 2017-04-26 CN disclosed
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 disclosed
US-20140275576-A1 PROCESS FOR THE PREPARATION OF (2,3-DIHYDRO-BENZO[B][1,4]DIOXIN-2-YL) METHANOL DERIVATIVES JANSSEN PHARMACEUTICA NV (BE) 2014-09-18 US disclosed
CN-1984906-A Condensed benzamide compounds and inhibitors of vanilloid receptor subtype 1 (VR1) activity JAPAN TOBACCO INC (JP) 2007-06-20 CN disclosed
CN-1139586-C Process for stereoselective preparation of hetero-bicyclic alcohol enantiomer �ŷƶ����ʿ������޹�˾ 2004-02-25 CN disclosed
CN-1160714-A Process for stereoselective preparation of hetero-bicyclic alcohol enantiomer DUPHAR INT RES (NL) 1997-10-01 CN disclosed
EP-0512020-A1 PROCESS FOR PREPARING HOMOCHIRAL AMINES AND PROCESS FOR PREPARING INTERMEDIATES FOR THE PREPARATION THEREOF Nobel Chemicals AB (SE) 1992-11-11 EP disclosed
WO-1991010642-A1 PROCESS FOR PREPARING HOMOCHIRAL AMINES AND PROCESS FOR PREPARING INTERMEDIATES FOR THE PREPARATION THEREOF, AND THE INTERMEDIATES PREPARED IN ACCORDANCE WITH THIS PROCESS NOBEL CHEMICALS AB (SE) 1991-07-25 WO 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 (8 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-12303474-B2 S-enantiomerically enriched compositions of beta blockers for treating amyotrophic lateral sclerosis SMN1; SMN2, CPT1B, ADRB1 PRMT5 2446/4885WDR77 755/4885PKM 3652/4885
US-20230279020-A9 CARM1 INHIBITORS AND USES THEREOF CARM1, TIAM1, ADRM1 PRMT5 79/4885WDR77 315/4885PKM 1173/4885
US-11834455-B2 Carm1 inhibitors and uses thereof CARM1, TIAM1, ADRM1 PRMT5 78/4885WDR77 311/4885PKM 1154/4885
US-11433036-B2 Oxprenolol compositions for treating cancer ADRB1, ADRB2, CPT1B PRMT5 3236/4885WDR77 658/4885PKM 1328/4885
US-11938102-B2 S-enantiomerically enriched compositions of beta blockers for treating amyotrophic lateral sclerosis SMN1; SMN2, CPT1B, ADRB1 PRMT5 2446/4885WDR77 755/4885PKM 3652/4885
US-20240325322-A1 S-ENANTIOMERICALLY ENRICHED COMPOSITIONS OF BETA BLOCKERS FOR TREATING AMYOTROPHIC LATERAL SCLEROSIS SMN1; SMN2, CPT1B, ADRB1 PRMT5 2446/4885WDR77 755/4885PKM 3652/4885
US-20140275576-A1 PROCESS FOR THE PREPARATION OF (2,3-DIHYDRO-BENZO[B][1,4]DIOXIN-2-YL) METHANOL DERIVATIVES CYP1B1, CYP1A1, CYP4B1 PRMT5 4038/4885WDR77 2902/4885PKM 2680/4885
US-20230416263-A1 CARM1 INHIBITORS AND USES THEREOF CARM1, TIAM1, ADRM1 PRMT5 79/4885WDR77 315/4885PKM 1173/4885

“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.