SCHEMBL30432086

SCHEMBL30432086

CC(C)C[C@H](NC(=O)CNC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@@H](NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@@H](N)CC(=O)O)[C@@H](C)O)[C@@H](C)O)C(C)C)C(=O)O

nearest known ligand 0.72

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
▸ RAMP3 O60896 3/20 0.63
▸ CALCR P30988 3/20 0.63
▸ NPY2R P49146 7/20 0.63
▸ NPY4R P50391 7/20 0.63
▸ NPY5R Q15761 7/20 0.63
▸ NPY1R P25929 5/20 0.63
▸ TFPI P10646 4/20 0.62
▸ EPHA2 P29317 2/20 0.61
▸ NMUR2 Q9GZQ4 2/20 0.61
▸ NMUR1 Q9HB89 2/20 0.61
▸ KEAP1 Q14145 1/20 0.60

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
SCHEMBL30495778 0.90 NPY2R (0.69) NPY2RNPY4RNPY5RNPY1RTFPI
SCHEMBL30423064 0.90 KEAP1 (0.69) RAMP3CALCRNPY2RNPY4RNPY5R
SCHEMBL30432104 0.90 TFPI (0.69) NPY2RNPY4RNPY5RNPY1RTFPI
SCHEMBL31182744 0.90 NPY2R (0.67) RAMP3CALCRNPY2RNPY4RNPY5R
SCHEMBL29364257 0.90 KEAP1 (0.59) NPY2RNPY4RNPY5RNPY1RTFPI
SCHEMBL30832038 0.90 EPHA2 (0.62) NPY2RNPY4RNPY5RNPY1RTFPI
SCHEMBL29939144 0.90 NPY2R (0.58) RAMP3CALCRNPY2RNPY4RNPY5R
SCHEMBL30607481 0.89 NPY2R (0.67) RAMP3CALCRNPY2RNPY4RNPY5R
SCHEMBL29649200 0.89 CALCR (0.60) CALCRNPY2RNPY4RNPY5RNPY1R
SCHEMBL32677401 0.89 NMUR2 (0.62) RAMP3CALCRNPY2RNPY4RNPY5R

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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