SCHEMBL30432597

SCHEMBL30432597

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

nearest known ligand 0.67

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
▸ NPY2R P49146 8/20 0.67
▸ NPY4R P50391 8/20 0.67
▸ NPY5R Q15761 8/20 0.67
▸ NPY1R P25929 6/20 0.67
▸ KDM1A O60341 3/20 0.62
▸ MAOB P27338 1/20 0.59
▸ KDM5A P29375 1/20 0.59
▸ KDM1B Q8NB78 1/20 0.59
▸ RAMP3 O60896 1/20 0.57
▸ CALCR P30988 1/20 0.57
▸ TFPI P10646 3/20 0.57
▸ EP300 Q09472 1/20 0.56
▸ HIF1A Q16665 1/20 0.56
▸ NTSR2 O95665 2/20 0.56
▸ NTSR1 P30989 2/20 0.56
▸ SORT1 Q99523 2/20 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
SCHEMBL30607435 0.90 NPY2R (0.76) NPY2RNPY4RNPY5RNPY1RKDM1A
SCHEMBL11150031 0.90 NPY2R (0.73) NPY2RNPY4RNPY5RNPY1RRAMP3
SCHEMBL30906497 0.90 NPY2R (0.69) NPY2RNPY4RNPY5RNPY1RRAMP3
SCHEMBL31182685 0.89 NPY2R (0.67) NPY2RNPY4RNPY5RNPY1RKDM1A
SCHEMBL30607396 0.89 NPY2R (0.65) NPY2RNPY4RNPY5RNPY1RKDM1A
SCHEMBL31182907 0.89 NPY2R (0.66) NPY2RNPY4RNPY5RNPY1RKDM1A
SCHEMBL30435649 0.88 NPY2R (0.68) NPY2RNPY4RNPY5RNPY1RKDM1A
SCHEMBL30906377 0.88 NPY2R (0.71) NPY2RNPY4RNPY5RNPY1RRAMP3
SCHEMBL30974622 0.88 KDM1A (0.62) NPY2RNPY4RNPY5RNPY1RKDM1A
SCHEMBL30495647 0.88 NPY2R (0.77) NPY2RNPY4RNPY5RNPY1RRAMP3

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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