SCHEMBL6862333

SCHEMBL6862333

CCOC(=O)CCN(C1(C(=O)O)CC2CCC(C1)O2)S(=O)(=O)c1ccc(Oc2ccc(F)cc2)cc1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MMP1 P03956 3/20 0.50
MMP13 P45452 2/20 0.45
MMP2 P08253 2/20 0.45
MMP9 P14780 2/20 0.45
MMP8 P22894 2/20 0.45
MMP3 P08254 1/20 0.45
SMN1; SMN2 Q16637 1/20 0.42
FFAR1 O14842 1/20 0.38
CETP P11597 1/20 0.38
POLB P06746 3/20 0.36
TP53 P04637 1/20 0.36
TDP1 Q9NUW8 1/20 0.36
LTA4H P09960 1/20 0.36
ALOX15 P16050 1/20 0.36
L3MBTL1 Q9Y468 2/20 0.35
NPSR1 Q6W5P4 2/20 0.35
MMP14 P50281 1/20 0.35
TAS2R14 Q9NYV8 1/20 0.34
NR3C1 P04150 1/20 0.34
MAPT P10636 1/20 0.33

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
SCHEMBL6871476 0.92 MMP1 (0.47) MMP1MMP13MMP2MMP9MMP8
SCHEMBL6992588 0.91 MMP1 (0.59) MMP1MMP13MMP2MMP9MMP8
SCHEMBL6870777 0.91 MMP1 (0.59) MMP1MMP13MMP2MMP9MMP8
SCHEMBL6689128 0.85 MMP1 (0.65) MMP1MMP13MMP2MMP9MMP8
SCHEMBL6809653 0.85 MMP1 (0.62) MMP1MMP13SMN1; SMN2FFAR1CETP
SCHEMBL6866226 0.85 MMP1 (0.55) MMP1MMP13MMP2MMP9MMP8
SCHEMBL6998236 0.82 MMP1 (0.54) MMP1MMP13MMP2MMP9MMP8
SCHEMBL6998238 0.82 MMP1 (0.54) MMP1MMP13MMP2MMP9MMP8
SCHEMBL27561065 0.81 MMP1 (0.56) MMP1MMP13SMN1; SMN2FFAR1CETP
SCHEMBL7003643 0.81 MMP1 (0.73) MMP1MMP13MMP2MMP9MMP8

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1068180-B1 PROCESS FOR ALKYLATING HINDERED SULFONAMIDES USEFUL IN THE PRODUCTION OF MATRIX METALLOPROTENASE INHIBITORS PFIZER PROD INC (US) 2004-12-15 EP disclosed
EP-0949245-B1 Process for alkylating hindered sulfonamides PFIZER PROD INC (US) 2001-10-04 EP disclosed
US-6288246-B1 REACTION OF HYDROXYLAMINE WITH ALKYLSILYL HALIDE, HYDROLYSIS WITH ACID PFIZER INC 2001-09-11 US disclosed
US-6229025-B1 MICHAEL ADDITION TO PROPIOLATES PFIZER INC 2001-05-08 US disclosed
US-6114568-A Process for alkylating hindered sulfonamides useful in the production of matrix metalloproteinase inhibitors PFIZER INC. (US) 2000-09-05 US disclosed
EP-0949244-A2 Process for preparing hydroxamic acids Pfizer Products Inc. (US) 1999-10-13 EP disclosed
EP-0949245-A1 Process for alkylating hindered sulfonamides Pfizer Products Inc. (US) 1999-10-13 EP disclosed