SCHEMBL30432655

SCHEMBL30432655

CC[C@H](C)[C@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H](N)C(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C)C(=O)NCC(=O)N[C@@H](CCCCN)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](CCCCN)C(=O)N[C@H](C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CO)C(=O)N[C@H](C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)O)[C@@H](C)O)[C@@H](C)O

nearest known ligand 0.65

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
▸ CALCR P30988 4/20 0.65
▸ CRHR1 P34998 1/20 0.63
▸ CRHR2 Q13324 1/20 0.63
▸ HCRTR1 O43613 1/20 0.63
▸ HCRTR2 O43614 1/20 0.63
▸ F2 P00734 4/20 0.59
▸ NPY2R P49146 7/20 0.57
▸ NPY4R P50391 7/20 0.57
▸ NPY5R Q15761 7/20 0.57
▸ NPY1R P25929 5/20 0.57
▸ CCKBR P32239 1/20 0.56
▸ GLP1R P43220 1/20 0.56

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
SCHEMBL30432477 0.89 CALCR (0.78) CALCRCRHR1CRHR2HCRTR1HCRTR2
SCHEMBL30431785 0.88 CALCR (0.68) CALCRCRHR1CRHR2HCRTR1HCRTR2
SCHEMBL30432821 0.87 CALCR (0.61) CALCRCRHR1CRHR2HCRTR1HCRTR2
SCHEMBL30432865 0.86 CALCR (0.76) CALCRCRHR1CRHR2HCRTR1HCRTR2
SCHEMBL29884239 0.86 CALCR (0.69) CALCRCRHR1CRHR2HCRTR1HCRTR2
SCHEMBL30712965 0.85 CALCR (0.71) CALCRCRHR1CRHR2HCRTR1HCRTR2
SCHEMBL30844080 0.85 CALCR (0.67) CALCRCRHR1CRHR2HCRTR1HCRTR2
SCHEMBL31182738 0.84 CALCR (0.67) CALCRCRHR1CRHR2HCRTR1HCRTR2
SCHEMBL31182828 0.84 CALCR (0.71) CALCRCRHR1CRHR2HCRTR1HCRTR2
SCHEMBL31683370 0.84 CALCR (0.70) CALCRCRHR1CRHR2HCRTR1HCRTR2

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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