SCHEMBL4909949

SCHEMBL4909949

O=S(=O)(O)Cc1noc2ccccc12.[NaH]

nearest known ligand 0.71

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 3/20 0.71
CA12 O43570 1/20 0.71
CA1 P00915 1/20 0.71
CA2 P00918 1/20 0.71
CA3 P07451 1/20 0.71
CA4 P22748 1/20 0.71
CA6 P23280 1/20 0.71
MAOB P27338 1/20 0.71
CA5A P35218 1/20 0.71
CA7 P43166 1/20 0.71
CA9 Q16790 1/20 0.71
CA13 Q8N1Q1 1/20 0.71
CA14 Q9ULX7 1/20 0.71
CA5B Q9Y2D0 1/20 0.71
SMN1; SMN2 Q16637 6/20 0.63
CYP3A4 P08684 1/20 0.63
BLM P54132 1/20 0.63
GAA P10253 2/20 0.48
RAB9A P51151 5/20 0.45
NPC1 O15118 4/20 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
SCHEMBL3239117 0.98 LMNA (0.73) LMNACA12CA1CA2CA3
SCHEMBL4916596 0.97 LMNA (0.71) LMNACA12CA1CA2CA3
Ammonia Solution, Strong SCHEMBL3237966 0.97 LMNA (0.71) LMNACA12CA1CA2CA3
Water SCHEMBL3264442 0.97 LMNA (0.71) LMNACA12CA1CA2CA3
SCHEMBL4913871 0.88 LMNA (0.60) LMNACA12CA1CA2CA3
Zonisamide SCHEMBL1321446 0.85 LMNA (0.97) LMNACA12CA1CA2CA3
SCHEMBL28155790 0.84 LMNA (0.55) LMNACA12CA1CA2CA3
Zonisamide SCHEMBL29358822 0.83 LMNA (1.00) LMNACA12CA1CA2CA3
Zonisamide SCHEMBL1816247 0.83 LMNA (1.00) LMNACA12CA1CA2CA3
Zonisamide SCHEMBL35458 0.83 LMNA (1.00) LMNACA12CA1CA2CA3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115770613-B Molecular sieve catalyst and preparation method thereof 江西省科学院应用化学研究所 2024-03-12 CN claimed
CN-115770613-A Molecular sieve catalyst and preparation method thereof 江西省科学院应用化学研究所 2023-03-10 CN claimed
WO-2007016209-A2 PURE 1,2-BENZISOXAZOLE-3-METHANE-SULFONIC ACID SODIUM SALT AND PURIFICATION PROCESS TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2007-02-08 WO claimed
CN-115770613-B Molecular sieve catalyst and preparation method thereof 江西省科学院应用化学研究所 2024-03-12 CN disclosed
CN-115770613-A Molecular sieve catalyst and preparation method thereof 江西省科学院应用化学研究所 2023-03-10 CN disclosed
EP-1728786-B1 ONE-POT PROCESS FOR PRODUCING 1,2-BENZISOXAZOLE-3-METHANESULFONAMIDE SUMITOMO DAINIPPON PHARMA CO LTD (JP) 2016-01-13 EP disclosed
CN-1934096-B Single-pot preparation method of 1, 2-benzisoxazole-3-methyl sulfonamide DAINIPPON SUMITOMO PHARMA CO 2012-04-18 CN disclosed
US-20080081914-A1 PROCESS FOR THE PREPARATION OF BENZO [D] ISOXAZOL-3-YL-METHANESULFONIC ACID AND THE INTERMEDIATES THEREOF DIPHARMA S.P.A. (IT) 2008-04-03 US disclosed
US-7291742-B2 Process for the preparation of benzo [d] isoxazol-3-yl-methanesulfonic acid and the intermediates thereof DIPHARMA S.P.A. (IT) 2007-11-06 US disclosed
US-7262304-B2 One-pot process for the preparation of 1,2-benzisoxazole-3-methanesulfonamide DAINIPPON SUMITOMO PHARMA CO., LTD. (JP) 2007-08-28 US disclosed
CN-1934096-A One-pot process for the preparation of 1,2-benzisoxazole-3-methanesulfonamide DAINIPPON SUMITOMO PHARMA CO (JP) 2007-03-21 CN disclosed
US-7081539-B2 One-pot process for the preparation of 1,2-benzisoxazole-3-methanesulfonamide DAINIPPON SUMITOMO PHARMA CO., LTD. (JP) 2006-07-25 US disclosed
US-20060135582-A1 Process for the preparation of benzo [d] isoxazol-3-yl-methanesulfonic acid and the intermediates thereof DIPHARMA S.P.A. (IT) 2006-06-22 US disclosed
EP-1581508-A1 A PROCESS FOR THE PREPARATION OF BENZO D ISOXAZOL-3-YL- METHANESULFONIC ACID AND THE INTERMEDIATES THEREOF Dipharma S.p.A. (IT) 2005-10-05 EP disclosed
US-20050215796-A1 One-pot process for the preparation of 1,2-benzisoxazole-3-methanesulfonamide Sumitomo Pharma Co., Ltd. (JP) 2005-09-29 US disclosed
WO-2005044808-A1 A PROCESS FOR THE MANUFACTURE OF ZONISAMIDE WOCKHARDT LIMITED (IN) 2005-05-19 WO disclosed
WO-2004063173-A1 A PROCESS FOR THE PREPARATION OF BENZO[D]ISOXAZOL-3-YL-METHANESULFONIC ACID AND THE INTERMEDIATES THEREOF DIPHARMA S.P.A. (IT) 2004-07-29 WO disclosed
US-20040049053-A1 Process for the prepartion of 1,2-benzisoxazole-3-acetic acid MENDELOVICI MARIOARA (IL) 2004-03-11 US disclosed
US-6677458-B2 REACTING 4-HYDROXY-COUMARIN WITH HYDROXYL-AMINE IN THE PRESENCE OF A BASE TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2004-01-13 US disclosed
US-20020183525-A1 Process for the preparation of 1,2-benzisoxazole-3-acetic acid TEVA PHARMACEUTICALS USA, INC. 2002-12-05 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 (4 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-20080081914-A1 PROCESS FOR THE PREPARATION OF BENZO [D] ISOXAZOL-3-YL-METHANESULFONIC ACID AND THE INTERMEDIATES THEREOF GABRD, GABRA5, GABRA6 LMNA 1596/4885CA12 933/4885CA1 229/4885
US-20040049053-A1 Process for the prepartion of 1,2-benzisoxazole-3-acetic acid HAO2, CYP4X1, CYP2S1 LMNA 1402/4885CA12 770/4885CA1 109/4885
US-20020183525-A1 Process for the preparation of 1,2-benzisoxazole-3-acetic acid HAO2, CYP2S1, CYP4X1 LMNA 2783/4885CA12 705/4885CA1 154/4885
US-20060135582-A1 Process for the preparation of benzo [d] isoxazol-3-yl-methanesulfonic acid and the intermediates thereof GABRD, GABRA5, GABRA6 LMNA 1596/4885CA12 933/4885CA1 229/4885

“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.