SCHEMBL30431785

SCHEMBL30431785

CC[C@H](C)[C@H](NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CO)NC(=O)[C@H](CO)NC(=O)CNC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](N)CCC(=O)O)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(=O)O)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)O

nearest known ligand 0.68

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
▸ CALCR P30988 4/20 0.68
▸ F2 P00734 4/20 0.68
▸ HCRTR1 O43613 1/20 0.67
▸ HCRTR2 O43614 1/20 0.67
▸ CRHR1 P34998 1/20 0.64
▸ CRHR2 Q13324 1/20 0.64
▸ NPY2R P49146 5/20 0.60
▸ NPY4R P50391 5/20 0.60
▸ NPY5R Q15761 5/20 0.60
▸ NPY1R P25929 4/20 0.60
▸ CCKBR P32239 2/20 0.59
▸ GLP1R P43220 2/20 0.59

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
SCHEMBL30712965 0.94 CALCR (0.71) CALCRF2HCRTR1HCRTR2CRHR1
SCHEMBL29884239 0.93 CALCR (0.69) CALCRF2HCRTR1HCRTR2CRHR1
SCHEMBL31683370 0.90 CALCR (0.70) CALCRF2HCRTR1HCRTR2CRHR1
SCHEMBL30932076 0.89 CALCR (0.82) CALCRF2HCRTR1HCRTR2CRHR1
SCHEMBL31182828 0.89 CALCR (0.71) CALCRF2HCRTR1HCRTR2CRHR1
SCHEMBL31603939 0.89 CALCR (0.70) CALCRF2HCRTR1HCRTR2CRHR1
SCHEMBL31182767 0.89 CALCR (0.67) CALCRF2HCRTR1HCRTR2CRHR1
SCHEMBL30804656 0.89 F2 (0.67) CALCRF2HCRTR1HCRTR2CRHR1
SCHEMBL30844080 0.88 CALCR (0.67) CALCRF2HCRTR1HCRTR2CRHR1
SCHEMBL30432054 0.88 F2 (0.66) CALCRF2HCRTR1HCRTR2CRHR1

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-20240342111-A1 ISOMER-SPECIFIC NEUROPROTECTIVE EFFECT OF NATURAL RESERVATROL UNIV SOUTH CAROLINA (US) 2024-10-17 — — US disclosed
US-20230201133-A1 Isomer-Specific Neuroprotective Effect of Natural Resveratrol UNIVERSITY OF SOUTH CAROLINA (US) 2023-06-29 — — US disclosed
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