Napsagatran Anhydrous

Napsagatran Anhydrous

SCHEMBL7294707

N=C(N)N1CCC[C@@H](CNC(=O)C[C@H](NS(=O)(=O)c2ccc3ccccc3c2)C(=O)N(CC(=O)O)C2CC2)C1

nearest known ligand 0.76

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Predicted protein targets (top 1)

geneUniProtsupporting neighboursconfidence
F2 P00734 20/20 0.76

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
Napsagatran Anhydrous SCHEMBL30693689 1.00 F2 (0.76) F2
Napsagatran Anhydrous SCHEMBL4427740 1.00 F2 (0.76) F2
Napsagatran Anhydrous SCHEMBL8947681 0.99 F2 (0.76) F2
Napsagatran Anhydrous SCHEMBL8947800 0.99 F2 (0.76) F2
Napsagatran Anhydrous SCHEMBL635609 0.99 F2 (0.75) F2
Napsagatran Anhydrous SCHEMBL8947631 0.99 F2 (0.76) F2
SCHEMBL7300991 0.98 F2 (0.75) F2
SCHEMBL7298126 0.97 F2 (0.76) F2
SCHEMBL7301035 0.92 F2 (0.75) F2
SCHEMBL8947770 0.92 F2 (0.63) F2

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
EP-0559046-B1 N-amidinopiperidinyl(3/4)- or N-amidino-1,4-Oxazinyl(2)-substituted sulfonamides, process for their preparation and use as thrombin inhibitors HOFFMANN LA ROCHE (CH) 2001-07-11 EP claimed
EP-0684238-A2 Process for the manufacture of dicarboxamides F. HOFFMANN-LA ROCHE AG (CH) 1995-11-29 EP claimed
US-5405854-A Anticoagulants HOFFMANN-LA ROCHE INC. (US) 1995-04-11 US claimed
EP-0559046-A1 N-amidinopiperidinyl(3/4)- or N-amidino-1,4-Oxazinyl(2)-substituted sulfonamides, process for their preparation and use as thrombin inhibitors F.HOFFMANN-LA ROCHE & CO. AKTIENGESELLSCHAFT (CH) 1993-09-08 EP claimed
EP-0559046-B1 N-amidinopiperidinyl(3/4)- or N-amidino-1,4-Oxazinyl(2)-substituted sulfonamides, process for their preparation and use as thrombin inhibitors HOFFMANN LA ROCHE (CH) 2001-07-11 EP disclosed
US-5578594-A ANTICOAGULANTS HOFFMANN-LA ROCHE INC. (US) 1996-11-26 US disclosed
US-5559232-A ANTICOAGULANTS HOFFMANN-LA ROCHE INC. (US) 1996-09-24 US disclosed
US-5536867-A Process for the manufacture of dicarboxamides HOFFMANN-LA ROCHE INC. (US) 1996-07-16 US disclosed
EP-0684238-A2 Process for the manufacture of dicarboxamides F. HOFFMANN-LA ROCHE AG (CH) 1995-11-29 EP disclosed
US-5405854-A Anticoagulants HOFFMANN-LA ROCHE INC. (US) 1995-04-11 US disclosed
EP-0641779-A1 Novel 1-amidinopiperdines and 4-amidinomorpholines as aggregation inhibitions F. HOFFMANN-LA ROCHE AG (CH) 1995-03-08 EP disclosed
EP-0559046-A1 N-amidinopiperidinyl(3/4)- or N-amidino-1,4-Oxazinyl(2)-substituted sulfonamides, process for their preparation and use as thrombin inhibitors F.HOFFMANN-LA ROCHE & CO. AKTIENGESELLSCHAFT (CH) 1993-09-08 EP disclosed