SCHEMBL336605

SCHEMBL336605

O=[N+]([O-])c1cccc(S(=O)(=O)OC[C@@H]2CO2)c1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PRMT5 O14744 1/20 1.00
WDR77 Q9BQA1 1/20 1.00
KMT2A Q03164 4/20 0.53
GAA P10253 1/20 0.53
HTT P42858 1/20 0.53
CA2 P00918 3/20 0.50
CA5A P35218 1/20 0.50
MEN1 O00255 3/20 0.49
LMNA P02545 1/20 0.47
MMP2 P08253 2/20 0.47
CA1 P00915 1/20 0.47
MMP1 P03956 1/20 0.47
MMP9 P14780 1/20 0.47
MMP8 P22894 1/20 0.47
MMP13 P45452 1/20 0.47
CA12 O43570 1/20 0.46
CA9 Q16790 1/20 0.46
ALDH1A1 P00352 1/20 0.46
ACHE P22303 1/20 0.45
CYP19A1 P11511 1/20 0.45

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
SCHEMBL29481767 1.00 PRMT5 (1.00) PRMT5WDR77KMT2AGAAHTT
SCHEMBL336603 1.00 PRMT5 (1.00) PRMT5WDR77KMT2AGAAHTT
SCHEMBL29476299 1.00 PRMT5 (1.00) PRMT5WDR77KMT2AGAAHTT
SCHEMBL449928 1.00 PRMT5 (1.00) PRMT5WDR77KMT2AGAAHTT
SCHEMBL30301224 1.00 PRMT5 (1.00) PRMT5WDR77KMT2AGAAHTT
SCHEMBL28711197 0.90 PRMT5 (0.81) PRMT5WDR77KMT2AGAAHTT
SCHEMBL29481804 0.90 PRMT5 (0.81) PRMT5WDR77KMT2AGAAHTT
SCHEMBL29502671 0.90 PRMT5 (0.81) PRMT5WDR77KMT2AGAAHTT
SCHEMBL28692108 0.90 PRMT5 (0.81) PRMT5WDR77KMT2AGAAHTT
SCHEMBL8265917 0.88 PRMT5 (0.79) PRMT5WDR77KMT2AGAAHTT

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 899 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
CN-118126009-A Coumarin derivative, preparation method and application 成都纽瑞特医疗科技股份有限公司 2024-06-04 CN claimed
CN-116178220-A Method for preparing (2S) -2- [ [3- (methylsulfonyl L) phenoxy ] methyl ] ethylene oxide 爱斯特(成都)生物制药股份有限公司 2023-05-30 CN claimed
EP-2860175-B1 METHOD FOR PRODUCING 4,4,7-TRIFLUORO-1,2,3,4-TETRAHYDRO-5H-1-BENZAZEPINE COMPOUND AND INTERMEDIATE FOR SYNTHESIS THEREOF TACURION (US) 2017-11-29 EP claimed
US-9598373-B2 Method for producing 4,4,7-trifluoro-1,2,3,4-tetrahydro-5H-1-benzazepine compound and intermediate used in the method TACURION (US) 2017-03-21 US claimed
US-20150141641-A1 METHOD FOR PRODUCING 4,4,7-TRIFLUORO-1,2,3,4-TETRAHYDRO-5H-1-BENZAZEPINE COMPOUND AND INTERMEDIATE USED IN THE METHOD ASTELLAS PHARMA INC. (JP) 2015-05-21 US claimed
EP-2860175-A1 METHOD FOR PRODUCING 4,4,7-TRIFLUORO-1,2,3,4-TETRAHYDRO-5H-1-BENZAZEPINE COMPOUND AND INTERMEDIATE FOR SYNTHESIS THEREOF Astellas Pharma Inc. (JP) 2015-04-15 EP claimed
CN-101768148-B New preparation method of hydrochloride landiolol TIANJIN HANKANG PHARMACEUTICAL BIOTECHNOLOGY CO LTD 2013-11-06 CN claimed
CN-101768148-A New preparation method of hydrochloride landiolol JIE YAN 2010-07-07 CN claimed
US-12617782-B2 Pyridazinones as PARP7 inhibitors RIBON THERAPEUTICS, INC. (US) 2026-05-05 US disclosed
US-20260027106-A1 PRMT5 INHIBITORS AND USES THEREOF Epizyme, Inc. 2026-01-29 US disclosed
CN-223299631-U A high-efficient purification device for 3-nitrobenzenesulfonic acid (S) -glycidyl ester 合肥康鸿生物科技有限公司 2025-09-05 CN disclosed
CN-223299631-U A high-efficient purification device for 3-nitrobenzenesulfonic acid (S) -glycidyl ester 合肥康鸿生物科技有限公司 2025-09-05 CN disclosed
CN-223069517-U 3-Nitrobenzenesulfonic acid (S) -glycidyl ester rapid reaction equipment 合肥康鸿生物科技有限公司 2025-07-08 CN disclosed
US-5053338-A Hydrolysis of ester to obtain an optically enriched mixture of a phenol enantiomer GLAXO INC. (US) 1991-10-01 US disclosed
US-5051431-A For treatment of congestive heart failure GLAXO INC. (US) 1991-09-24 US 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
EP-0419286-A2 Pyridone nitriles useful in treating cardiovascular disease GLAXO WELLCOME INC. (US) 1991-03-27 EP disclosed
EP-0412814-A2 Pyridazinones having cardiotonic and beta blocking activity GLAXO WELLCOME INC. (US) 1991-02-13 EP disclosed
WO-1988000190-A1 OPTICALLY ACTIVE DERIVATIVES OF GLYCIDOL MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) 1988-01-14 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-20260027106-A1 PRMT5 INHIBITORS AND USES THEREOF PRMT5, PRMT1, PRMT3 PRMT5 1/4885WDR77 158/4885KMT2A 155/4885
US-20150141641-A1 METHOD FOR PRODUCING 4,4,7-TRIFLUORO-1,2,3,4-TETRAHYDRO-5H-1-BENZAZEPINE COMPOUND AND INTERMEDIATE USED IN THE METHOD AVPR2, AVPR1A, AVPR1B PRMT5 81/4885WDR77 3453/4885KMT2A 1807/4885
US-12617782-B2 Pyridazinones as PARP7 inhibitors PARP3, PARP2, PARP1 PRMT5 3370/4885WDR77 1889/4885KMT2A 1790/4885

“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.