SCHEMBL30432496

SCHEMBL30432496

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

nearest known ligand 0.67

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
▸ CALCR P30988 4/20 0.67
▸ HCRTR1 O43613 1/20 0.63
▸ HCRTR2 O43614 1/20 0.63
▸ CRHR1 P34998 1/20 0.62
▸ CRHR2 Q13324 1/20 0.62
▸ F2 P00734 4/20 0.59
▸ CCKBR P32239 2/20 0.58
▸ GLP1R P43220 2/20 0.58
▸ NPY2R P49146 7/20 0.58
▸ NPY4R P50391 7/20 0.58
▸ NPY5R Q15761 7/20 0.58
▸ NPY1R P25929 5/20 0.58

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
SCHEMBL30431785 0.87 CALCR (0.68) CALCRHCRTR1HCRTR2CRHR1CRHR2
SCHEMBL31182578 0.87 CRHR1 (0.66) CALCRHCRTR1HCRTR2CRHR1CRHR2
SCHEMBL31182828 0.87 CALCR (0.71) CALCRHCRTR1HCRTR2CRHR1CRHR2
SCHEMBL30536330 0.87 CALCR (0.66) CALCRHCRTR1HCRTR2CRHR1CRHR2
SCHEMBL31683370 0.87 CALCR (0.70) CALCRHCRTR1HCRTR2CRHR1CRHR2
SCHEMBL31182543 0.87 CALCR (0.79) CALCRHCRTR1HCRTR2CRHR1CRHR2
SCHEMBL30658230 0.87 CALCR (0.79) CALCRHCRTR1HCRTR2CRHR1CRHR2
SCHEMBL30254266 0.86 CALCR (0.64) CALCRHCRTR1HCRTR2CRHR1CRHR2
SCHEMBL30712965 0.86 CALCR (0.71) CALCRHCRTR1HCRTR2CRHR1CRHR2
SCHEMBL31182521 0.86 F2 (0.73) CALCRHCRTR1HCRTR2CRHR1CRHR2

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
Send feedback