SCHEMBL3586346

SCHEMBL3586346

C[S+]([O-])c1ccc([N+](=O)[O-])cc1F

nearest known ligand 0.50

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 7/20 0.50
HIF1A Q16665 1/20 0.50
TSHR P16473 4/20 0.44
TDP1 Q9NUW8 3/20 0.44
KMT2A Q03164 2/20 0.42
CYP3A4 P08684 2/20 0.42
LMNA P02545 2/20 0.41
HSD17B10 Q99714 2/20 0.40
ACHE P22303 2/20 0.39
PTPRC P08575 1/20 0.39
S100A4 P26447 1/20 0.39
S1PR4 O95977 1/20 0.39
HSPB1 P04792 2/20 0.39
HTT P42858 1/20 0.39
MEN1 O00255 1/20 0.38
NPC1 O15118 1/20 0.38
MAPT P10636 1/20 0.38
RAB9A P51151 1/20 0.38
SMN1; SMN2 Q16637 1/20 0.38

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
SCHEMBL24900737 0.87 ALDH1A1 (0.56) ALDH1A1HIF1ATSHRTDP1KMT2A
SCHEMBL27671923 0.81 ALDH1A1 (0.46) ALDH1A1HIF1ATSHRTDP1KMT2A
SCHEMBL13630905 0.80 TDP1 (0.53) ALDH1A1HIF1ATSHRTDP1KMT2A
SCHEMBL3572666 0.80 ALDH1A1 (0.60) ALDH1A1TSHRTDP1KMT2ACYP3A4
SCHEMBL30168212 0.80 ALDH1A1 (0.60) ALDH1A1TSHRTDP1KMT2ACYP3A4
SCHEMBL30142204 0.79 HSD17B10 (0.58) ALDH1A1TSHRTDP1KMT2ACYP3A4
SCHEMBL30168161 0.79 ALDH1A1 (0.46) ALDH1A1HIF1ATSHRTDP1CYP3A4
SCHEMBL2815988 0.79 ALDH1A1 (0.46) ALDH1A1HIF1ATSHRTDP1CYP3A4
SCHEMBL29883144 0.78 ALDH1A1 (0.41) ALDH1A1HIF1ATSHRTDP1CYP3A4
SCHEMBL23580535 0.78 ALDH1A1 (0.41) ALDH1A1HIF1ATSHRTDP1CYP3A4

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 12 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8507510-B2 Sulfoximine-substituted pyrimidines as CDK- and/or VEGF inhibitors, their production and use as pharmaceutical agents BAYER INTELLECTUAL PROPERTY GMBH (DE) 2013-08-13 US disclosed
US-8507510-B2 Sulfoximine-substituted pyrimidines as CDK- and/or VEGF inhibitors, their production and use as pharmaceutical agents BAYER INTELLECTUAL PROPERTY GMBH (DE) 2013-08-13 US disclosed
US-20100076000-A1 SULFOXIMINE-SUBSTITUTED PYRIMIDINES AS CDK- AND/OR VEGF INHIBITORS, THEIR PRODUCTION AND USE AS PHARMACEUTICAL AGENTS BAYER SCHERING PHARMA AKTIENGESELLSCHAFT 2010-03-25 US disclosed
US-20100076000-A1 SULFOXIMINE-SUBSTITUTED PYRIMIDINES AS CDK- AND/OR VEGF INHIBITORS, THEIR PRODUCTION AND USE AS PHARMACEUTICAL AGENTS BAYER SCHERING PHARMA AKTIENGESELLSCHAFT 2010-03-25 US disclosed
EP-1673352-B1 SULFOXIMINE-SUBSTITUTED PYRIMIDINES FOR USE AS CD AND/OR VEGF-INHIBITORS, THE PRODUCTION THEREOF AND THEIR USE AS DRUGS BAYER SCHERING PHARMA AG (DE) 2009-04-08 EP disclosed
US-7338958-B2 Sulfoximine-substituted pyrimidines as CDK-and/or VEGF inhibitors, their production and use as pharmaceutical agents SCHERING AG (DE) 2008-03-04 US disclosed
US-7338958-B2 Sulfoximine-substituted pyrimidines as CDK-and/or VEGF inhibitors, their production and use as pharmaceutical agents SCHERING AG (DE) 2008-03-04 US disclosed
US-20070191393-A1 Macrocyclic anilinopyrimidines with substituted sulphoximine as selective inhibitors of cell cycle kinases BAYER SCHERING PHARMA AKTIENGESELLSCHAFT (DE) 2007-08-16 US disclosed
WO-2007079982-A1 (2 , 4 , 9-TRIAZA-1 (2 , 4 ) -PYRIMIDINA-3 ( 1 , 3 ) -BENZENACYCLONONAPHANE-3 4-YL) -SULFOXIMINE DERIVATIVES AS SELECTIVE AURORA KINASE INHIBITORS FOR THE TREATMENT OF CANCER BAYER SCHERING PHARMA AKTIENGESELLSCHAFT (DE) 2007-07-19 WO disclosed
EP-1673352-A1 SULFOXIMINE-SUBSTITUTED PYRIMIDINES FOR USE AS CDK AND/OR VEGF INHIBITORS, THE PRODUCTION THEREOF AND THEIR USE AS DRUGS SCHERING AKTIENGESELLSCHAFT (DE) 2006-06-28 EP disclosed
US-20050176743-A1 Sulfoximine-substituted pyrimidines as CDK-and/or VEGF inhibitors, their production and use as pharmaceutical agents BAYER INTELLECTUAL PROPERTY GMBH (DE) 2005-08-11 US disclosed
WO-2005037800-A1 SULFOXIMINE-SUBSTITUTED PYRIMIDINES FOR USE AS CDK AND/OR VEGF INHIBITORS, THE PRODUCTION THEREOF AND THEIR USE AS DRUGS SCHERING AKTIENGESELLSCHAFT (DE) 2005-04-28 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-20050176743-A1 Sulfoximine-substituted pyrimidines as CDK-and/or VEGF inhibitors, their production and use as pharmaceutical agents CDK2, CDK1, FLT1 ALDH1A1 2681/4885HIF1A 404/4885TSHR 594/4885
US-20100076000-A1 SULFOXIMINE-SUBSTITUTED PYRIMIDINES AS CDK- AND/OR VEGF INHIBITORS, THEIR PRODUCTION AND USE AS PHARMACEUTICAL AGENTS CDK2, CDK1, FLT1 ALDH1A1 2681/4885HIF1A 404/4885TSHR 594/4885
US-20070191393-A1 Macrocyclic anilinopyrimidines with substituted sulphoximine as selective inhibitors of cell cycle kinases CCNI, CDK2, CDK1 ALDH1A1 3242/4885HIF1A 2101/4885TSHR 3381/4885

“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.