SCHEMBL5653246

SCHEMBL5653246

O=C=NS(=O)(=O)c1ccc([N+](=O)[O-])cc1

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
F2 P00734 3/20 0.56
PRSS1 P07477 3/20 0.56
PRSS2 P07478 3/20 0.56
PRSS3 P35030 3/20 0.56
CA2 P00918 9/20 0.52
CA1 P00915 8/20 0.52
CA9 Q16790 7/20 0.52
CA12 O43570 6/20 0.52
CA14 Q9ULX7 4/20 0.52
CA3 P07451 3/20 0.52
CA4 P22748 3/20 0.52
CA6 P23280 3/20 0.52
CA5A P35218 3/20 0.52
CA7 P43166 3/20 0.52
CA13 Q8N1Q1 3/20 0.52
CA5B Q9Y2D0 3/20 0.52
MMP1 P03956 1/20 0.47
MMP2 P08253 1/20 0.47
MMP9 P14780 1/20 0.47
MMP8 P22894 1/20 0.47

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
SCHEMBL5653955 0.83 F2 (0.37) F2PRSS1PRSS2PRSS3ALDH1A1
SCHEMBL29395884 0.83 F2 (0.54) F2PRSS1PRSS2PRSS3CA2
SCHEMBL5654389 0.81 KMT2A (0.62) F2PRSS1PRSS2PRSS3CA2
SCHEMBL10494209 0.79 F2 (0.63) F2PRSS1PRSS2PRSS3CA2
SCHEMBL10531766 0.78 F2 (0.67) F2PRSS1PRSS2PRSS3CA2
SCHEMBL11007951 0.76 ALDH1A1 (0.50) CA2CA1CA9CA12ALDH1A1
SCHEMBL10864649 0.76 LMNA (0.43) F2PRSS1PRSS2PRSS3CA2
SCHEMBL5654867 0.74 VCAM1 (0.40) F2PRSS1PRSS2PRSS3CA2
SCHEMBL5655146 0.74 F2 (0.52) F2PRSS1PRSS2PRSS3CA2
SCHEMBL22302 0.74 F2 (0.52) F2PRSS1PRSS2PRSS3CA2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9233943-B2 Process for synthesis of syn azido epdxide and its use as intermediate for the synthesis of amprenavir and saquinavir COUNCIL OF SCIENTIFIC & INDUSTRIAL RESEARCH (IN) 2016-01-12 US claimed
US-20150011782-A1 PROCESS FOR SYNTHESIS OF SYN AZIDO EPOXIDE AND ITS USE AS INTERMEDIATE FOR THE SYNTHESIS OF AMPRENAVIR & SAQUINAVIR COUNCIL OF SCIENTIFIC & INDUSTRIAL RESEARCH (IN) 2015-01-08 US claimed
US-4310459-A Process for producing carbamoyl substituted penams and carbamoyl substituted cephams from penicillin sulfoxide esters BRISTOL-MYERS COMPANY (US) 1982-01-12 US claimed
US-12615430-B2 Neural network device and control method Sony Group Corporation (JP) 2026-04-28 US disclosed
US-12263590-B2 Machine vision parsing of three-dimensional environments employing neural networks SANCTUARY COGNITIVE SYSTEMS CORPORATION (CA) 2025-04-01 US disclosed
US-20240414428-A1 NEURAL NETWORK DEVICE, CONTROL METHOD, AND PROGRAM Sony Group Corporation (JP) 2024-12-12 US disclosed
WO-2023074414-A1 NEURAL NETWORK DEVICE, CONTROL METHOD, AND PROGRAM ソニーグループ株式会社 2023-05-04 WO disclosed
US-9233943-B2 Process for synthesis of syn azido epdxide and its use as intermediate for the synthesis of amprenavir and saquinavir COUNCIL OF SCIENTIFIC & INDUSTRIAL RESEARCH (IN) 2016-01-12 US disclosed
US-20150011782-A1 PROCESS FOR SYNTHESIS OF SYN AZIDO EPOXIDE AND ITS USE AS INTERMEDIATE FOR THE SYNTHESIS OF AMPRENAVIR & SAQUINAVIR COUNCIL OF SCIENTIFIC & INDUSTRIAL RESEARCH (IN) 2015-01-08 US disclosed
WO-2013105118-A1 A PROCESS FOR SYNTHESIS OF SYN AZIDO EPOXIDE AND ITS USE AS INTERMEDIATE THE SYNTHESIS OF AMPRENAVIR & SAQUINAVIR COUNCIL OF SCIENTIFIC & INDUSTRIAL RESEARCH (IN) 2013-07-18 WO disclosed
US-7030274-B2 Process for the production of carbodiimide modified organic isocyanates BAYER MATERIALSCIENCE LLC (US) 2006-04-18 US disclosed
EP-0132675-A2 Preparations of polyisocynate containing reversibly blocked catalysts, process for their production, their use in the production of polyurethanes, and addition products of sulfonylisocyanates on catalysts with a structure of carboxylates of tin II or IV BAYER AG (DE) 1985-02-13 EP disclosed
US-4426520-A CEPHALOSPORIN ANTIBIOTICS BRISTOL-MYERS COMPANY (US) 1984-01-17 US disclosed
US-4407755-A BACTERICIDAL PENICILLINS BRISTOL-MYERS COMPANY (US) 1983-10-04 US disclosed
US-4374982-A Cepham compounds BRISTOL-MYERS COMPANY (US) 1983-02-22 US disclosed
US-4322347-A 2-Carbamoyloxymethyl-penicillin derivatives BRISTOL-MYERS COMPANY (US) 1982-03-30 US disclosed
US-4310459-A Process for producing carbamoyl substituted penams and carbamoyl substituted cephams from penicillin sulfoxide esters BRISTOL-MYERS COMPANY (US) 1982-01-12 US disclosed
US-4113734-A Masked isocyanates AGFA-GEVAERT, N.V. (BE) 1978-09-12 US disclosed
US-4073767-A Hydrogen phosphonates and polymers containing them as flame retardants MONSANTO COMPANY (US) 1978-02-14 US disclosed
US-3971740-A DYES FOR POLYESTER FIBERS CIBA-GEIGY AG (CH) 1976-07-27 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 (2 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-12615430-B2 Neural network device and control method NCDN, POU2F1, POU2F2 F2 3911/4885PRSS1 2098/4885PRSS2 2323/4885
US-20150011782-A1 PROCESS FOR SYNTHESIS OF SYN AZIDO EPOXIDE AND ITS USE AS INTERMEDIATE FOR THE SYNTHESIS OF AMPRENAVIR & SAQUINAVIR POR, CYP3A4, CYP2S1 F2 950/4885PRSS1 249/4885PRSS2 801/4885

“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.