SCHEMBL5227239

SCHEMBL5227239

Nc1nc(S(=O)(=O)Nc2ccccc2)n[nH]1

nearest known ligand 0.50

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
GAA P10253 1/20 0.50
GFER P55789 1/20 0.50
KMT2A Q03164 2/20 0.47
KEAP1 Q14145 3/20 0.46
IL1RN P18510 1/20 0.46
ERAP1 Q9NZ08 1/20 0.46
POLB P06746 1/20 0.44
MEN1 O00255 1/20 0.43
ALDH1A1 P00352 1/20 0.43
PKM P14618 1/20 0.43
CA1 P00915 3/20 0.43
CA2 P00918 3/20 0.43
SGK1 O00141 1/20 0.42
HTR6 P50406 1/20 0.41
KIT P10721 1/20 0.40
KDR P35968 1/20 0.40
CA12 O43570 2/20 0.40
CA9 Q16790 2/20 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
SCHEMBL9352767 0.84 CA1 (0.46) KMT2APOLBMEN1PKMCA1
SCHEMBL9041576 0.83 CYP3A4 (0.56) GAAKMT2AMEN1ALDH1A1PKM
SCHEMBL8313948 0.77 GAA (0.38) GAAKMT2A
Hydrochloric Acid SCHEMBL9169451 0.76 GAA (0.37) GAAKMT2A
SCHEMBL9247576 0.75 PKM (0.46) KMT2AMEN1PKM
SCHEMBL7472648 0.75 LMNA (0.51) KMT2AMEN1ALDH1A1
SCHEMBL10546861 0.74 TSHR (0.50) GAAGFERKMT2AKEAP1IL1RN
SCHEMBL9865806 0.73 SLC40A1 (0.38) GAAKMT2AALDH1A1
SCHEMBL10541111 0.71 KMT2A (0.47) KMT2AKEAP1IL1RNERAP1POLB
SCHEMBL6431253 0.70 KEAP1 (0.57) KMT2AKEAP1IL1RNERAP1POLB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1296962-B1 METHOD FOR PREPARING SUBSTITUTED 5-AMINO-N-PHENYL-1,2,4-TRIAZOLE-3-SULFONAMIDES BAYER CROPSCIENCE AG (DE) 2007-09-05 EP claimed
US-6680388-B2 HEATING 2,6-DICHLORO-3-METHYLANILINE WITH 5-AMINO-3-CHLORO-SULFONYL-1,2,4-TRIAZOLE, TO FORM CHEMICAL INTERMEDIATES FOR TRIAZOLO(1,5-A)PYRIMIDINE HERBICIDES BAYER CROPSCIENCE AG (DE) 2004-01-20 US claimed
US-20030162975-A1 Method for preparing substituted 5-amino-n-phenyl-1,2,4-triazole-3-sulfonamides BAYER INTELLECTUAL PROPERTY GMBH (DE) 2003-08-28 US claimed
EP-1296962-A1 METHOD FOR PREPARING SUBSTITUTED 5-AMINO-N-PHENYL-1,2,4-TRIAZOLE-3-SULFONAMIDES Bayer Aktiengesellschaft (DE) 2003-04-02 EP claimed
WO-2001096316-A1 METHOD FOR PREPARING SUBSTITUTED 5-AMINO-N-PHENYL-1,2,4-TRIAZOLE-3-SULFONAMIDES BAYER CROPSCIENCE AG (DE) 2001-12-20 WO claimed
EP-1296962-B1 METHOD FOR PREPARING SUBSTITUTED 5-AMINO-N-PHENYL-1,2,4-TRIAZOLE-3-SULFONAMIDES BAYER CROPSCIENCE AG (DE) 2007-09-05 EP disclosed
EP-1296962-B1 METHOD FOR PREPARING SUBSTITUTED 5-AMINO-N-PHENYL-1,2,4-TRIAZOLE-3-SULFONAMIDES BAYER CROPSCIENCE AG (DE) 2007-09-05 EP disclosed
EP-1296962-B1 METHOD FOR PREPARING SUBSTITUTED 5-AMINO-N-PHENYL-1,2,4-TRIAZOLE-3-SULFONAMIDES BAYER CROPSCIENCE AG (DE) 2007-09-05 EP disclosed
US-6680388-B2 HEATING 2,6-DICHLORO-3-METHYLANILINE WITH 5-AMINO-3-CHLORO-SULFONYL-1,2,4-TRIAZOLE, TO FORM CHEMICAL INTERMEDIATES FOR TRIAZOLO(1,5-A)PYRIMIDINE HERBICIDES BAYER CROPSCIENCE AG (DE) 2004-01-20 US disclosed
US-6680388-B2 HEATING 2,6-DICHLORO-3-METHYLANILINE WITH 5-AMINO-3-CHLORO-SULFONYL-1,2,4-TRIAZOLE, TO FORM CHEMICAL INTERMEDIATES FOR TRIAZOLO(1,5-A)PYRIMIDINE HERBICIDES BAYER CROPSCIENCE AG (DE) 2004-01-20 US disclosed
US-6680388-B2 HEATING 2,6-DICHLORO-3-METHYLANILINE WITH 5-AMINO-3-CHLORO-SULFONYL-1,2,4-TRIAZOLE, TO FORM CHEMICAL INTERMEDIATES FOR TRIAZOLO(1,5-A)PYRIMIDINE HERBICIDES BAYER CROPSCIENCE AG (DE) 2004-01-20 US disclosed
US-20030162975-A1 Method for preparing substituted 5-amino-n-phenyl-1,2,4-triazole-3-sulfonamides BAYER INTELLECTUAL PROPERTY GMBH (DE) 2003-08-28 US disclosed
CN-1436177-A Method for preparing substd.5-amino-N-pheny1-1,2,4, -triazole-3-sulfonamides BAYER CROP SCI AG (DE) 2003-08-13 CN disclosed
CN-1436177-A Method for preparing substd.5-amino-N-pheny1-1,2,4, -triazole-3-sulfonamides BAYER CROP SCI AG (DE) 2003-08-13 CN disclosed
EP-1296962-A1 METHOD FOR PREPARING SUBSTITUTED 5-AMINO-N-PHENYL-1,2,4-TRIAZOLE-3-SULFONAMIDES Bayer Aktiengesellschaft (DE) 2003-04-02 EP disclosed
EP-1296962-A1 METHOD FOR PREPARING SUBSTITUTED 5-AMINO-N-PHENYL-1,2,4-TRIAZOLE-3-SULFONAMIDES Bayer Aktiengesellschaft (DE) 2003-04-02 EP disclosed
EP-1296962-A1 METHOD FOR PREPARING SUBSTITUTED 5-AMINO-N-PHENYL-1,2,4-TRIAZOLE-3-SULFONAMIDES Bayer Aktiengesellschaft (DE) 2003-04-02 EP disclosed
WO-2001096316-A1 METHOD FOR PREPARING SUBSTITUTED 5-AMINO-N-PHENYL-1,2,4-TRIAZOLE-3-SULFONAMIDES BAYER CROPSCIENCE AG (DE) 2001-12-20 WO disclosed
WO-2001096316-A1 METHOD FOR PREPARING SUBSTITUTED 5-AMINO-N-PHENYL-1,2,4-TRIAZOLE-3-SULFONAMIDES BAYER CROPSCIENCE AG (DE) 2001-12-20 WO disclosed
WO-2001096316-A1 METHOD FOR PREPARING SUBSTITUTED 5-AMINO-N-PHENYL-1,2,4-TRIAZOLE-3-SULFONAMIDES BAYER CROPSCIENCE AG (DE) 2001-12-20 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 (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-20030162975-A1 Method for preparing substituted 5-amino-n-phenyl-1,2,4-triazole-3-sulfonamides CBR3, NAT1, SULT1A1 GAA 3814/4885GFER 696/4885KMT2A 1524/4885

“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.