SCHEMBL7436682

SCHEMBL7436682

CC(C)C[C@H](O)C(O)[C@H](CC1CCCCC1)N(C(=O)[C@H](Cc1ccccc1)NS(=O)(=O)N1CCOCC1)[C@H](Cc1csc(N)n1)C(N)=O

nearest known ligand 0.73

Predicted protein targets (top 1)

geneUniProtsupporting neighboursconfidence
▸ REN P00797 20/20 0.73

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
SCHEMBL9458635 0.84 REN (1.00) REN
SCHEMBL9322087 0.83 REN (0.54) REN
SCHEMBL9458632 0.81 REN (0.58) REN
SCHEMBL7320803 0.79 REN (0.57) REN
SCHEMBL9388320 0.72 REN (0.48) REN
SCHEMBL8955003 0.71 REN (0.66) REN
SCHEMBL9556735 0.71 REN (0.50) REN
SCHEMBL9322207 0.71 REN (0.67) REN
SCHEMBL8904006 0.70 REN (0.69) REN
SCHEMBL7392080 0.70 REN (0.50) REN

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0634175-B1 Pharmaceutical combination, containing a renin-angiotensin-system inhibitor and an endothelin antagonist HOFFMANN LA ROCHE (CH) 2001-01-10 — — EP disclosed
EP-0892783-A1 CARBOXYLIC ACID DERIVATIVES WITH AN AGGREGATION-INHIBITING ACTION Dr. Karl Thomae GmbH (DE) 1999-01-27 — — EP disclosed
WO-1997037975-A1 CARBOXYLIC ACID DERIVATIVES WITH AN AGGREGATION-INHIBITING ACTION DR. KARL THOMAE GMBH (DE) 1997-10-16 — — WO disclosed
EP-0581899-A1 IMPROVED PROCESS FOR THE PREPARATION OF 1S-(1R*, 2S*, 3R*)]-N-(4-(MORPHOLINYLSULFONYL)-L-PHENYLALANYL-3-(2-AMINO-4-THIAZOLYL)-N- (1-CYCLOHEXYLMETHYL)-2,3-DIHYDROXY-5-METHYLHEXYL]-L-ALANINAMIDE WARNER-LAMBERT COMPANY (US) 1994-02-09 — — EP disclosed
US-5268483-A Process for the preparation of an L-alanine compound WARNER-LAMBERT COMPANY (US) 1993-12-07 — — US disclosed
US-5220031-A Process for the preparation of [1S-(1R*,2S*3R*)]-N-(4-morpholinylsulfonyl)-L-phenylalanyl-3-(2-amino-4-thiazolyl-N-[(cyclohexylmethyl)-2,3-dihydroxy-5-methylhexyl]-L-alaninamide WARNER-LAMBERT COMPANY (US) 1993-06-15 — — US disclosed
US-5220031-A Process for the preparation of [1S-(1R*,2S*3R*)]-N-(4-morpholinylsulfonyl)-L-phenylalanyl-3-(2-amino-4-thiazolyl-N-[(cyclohexylmethyl)-2,3-dihydroxy-5-methylhexyl]-L-alaninamide WARNER-LAMBERT COMPANY (US) 1993-06-15 — — US disclosed
WO-1992018486-A1 IMPROVED PROCESS FOR THE PREPARATION OF [1S-(1R*, 2S*, 3R*)]-N-(4-(MORPHOLINYLSULFONYL)-L-PHENYLALANYL-3-(2-AMINO-4-THIAZOLYL)-N-[(1-CYCLOHEXYLMETHYL)-2,3-DIHYDROXY-5-METHYLHEXYL]-L-ALANINAMIDE WARNER-LAMBERT COMPANY (US) 1992-10-29 — — WO disclosed
US-5089616-A Process for the preparation of [1S-(1R*,2S*,3R*)]-N-(4-morpholinylsulfonyl)-L-phenylalanyl-3-(2-amino-4-thiazolyl-N-[(1-cyclohexylmethyl)-2,3-dihydroxy-5-methylhexyl]-L-alaninamide WARNER-LAMBERT COMPANY (US) 1992-02-18 — — US disclosed
US-5089616-A Process for the preparation of [1S-(1R*,2S*,3R*)]-N-(4-morpholinylsulfonyl)-L-phenylalanyl-3-(2-amino-4-thiazolyl-N-[(1-cyclohexylmethyl)-2,3-dihydroxy-5-methylhexyl]-L-alaninamide WARNER-LAMBERT COMPANY (US) 1992-02-18 — — US disclosed
Send feedback