SCHEMBL14560079

SCHEMBL14560079

C=COCCN(CCCCO)S(=O)(=O)c1ccc(OC)cc1

nearest known ligand 0.63

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
▸ MMP1 P03956 1/20 0.49
▸ MMP7 P09237 1/20 0.49
▸ MMP8 P22894 1/20 0.49
▸ MMP12 P39900 1/20 0.49
▸ MMP13 P45452 1/20 0.49
▸ SMN1; SMN2 Q16637 1/20 0.49
▸ BMP1 P13497 8/20 0.46
▸ CNR2 P34972 1/20 0.44
▸ MMP3 P08254 1/20 0.43
▸ MEP1B Q16820 1/20 0.43
▸ TAS2R14 Q9NYV8 2/20 0.43
▸ KEAP1 Q14145 2/20 0.42
▸ NFE2L2 Q16236 1/20 0.42
▸ ALDH1A1 P00352 2/20 0.42
▸ HPGD P15428 1/20 0.42

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
SCHEMBL4928380 0.93 SMN1; SMN2 (0.58) MMP1MMP7MMP8MMP12MMP13
SCHEMBL17230532 0.78 BMP1 (0.55) MMP1MMP7MMP8MMP12MMP13
SCHEMBL4936946 0.78 SMN1; SMN2 (0.77) MMP1MMP7MMP8MMP12MMP13
SCHEMBL6324195 0.77 SMN1; SMN2 (0.65) MMP1MMP7MMP8MMP12MMP13
SCHEMBL13979922 0.74 CNR2 (0.61) MMP1MMP7MMP8MMP12MMP13
SCHEMBL14229338 0.72 TAS2R14 (0.62) MMP1MMP7MMP8MMP12MMP13
SCHEMBL10385428 0.72 BMP1 (0.51) MMP1MMP7MMP8MMP12MMP13
SCHEMBL26483278 0.71 MEN1 (0.59) MMP1MMP7MMP8MMP12MMP13
SCHEMBL6325862 0.70 BMP1 (0.63) MMP1MMP7MMP8MMP12MMP13
SCHEMBL3615482 0.70 BMP1 (0.55) MMP1MMP7MMP8MMP12MMP13

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7186709-B2 Subjecting a vinyl ethers and an unsaturated ketoester to suitable conditions to generate a scaffold having the core dihydropyrancarboxamide or dihydropyrancarboxylic ester or acid; anticarcinogenic agents PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2007-03-06 — — US disclosed
US-7186709-B2 Subjecting a vinyl ethers and an unsaturated ketoester to suitable conditions to generate a scaffold having the core dihydropyrancarboxamide or dihydropyrancarboxylic ester or acid; anticarcinogenic agents PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2007-03-06 — — US disclosed
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