SCHEMBL28053702

C[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CS)NC(=O)[C@@H](N)Cc1ccccc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CO)C(=O)O

nearest known ligand 0.58

Predicted protein targets (top 5)

	gene	UniProt	supporting neighbours	confidence
▸	NPY4R	P50391	13/20	0.58

▸	NPY1R	P25929	8/20	0.58

▸	NPY5R	Q15761	7/20	0.58

▸	NPY2R	P49146	4/20	0.58

▸	KISS1R	Q969F8	5/20	0.54

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.

Compound	similarity	top predicted	shared targets
SCHEMBL30603887	0.91	NPY4R (0.63)	NPY4RNPY1RNPY5RNPY2R
SCHEMBL30452414	0.91	NPY4R (0.59)	NPY4RNPY1RNPY5RNPY2R
SCHEMBL30924738	0.89	NPY4R (0.62)	NPY4RNPY1RNPY5RNPY2RKISS1R
SCHEMBL30265009	0.89	NPY4R (0.58)	NPY4RNPY1RNPY5RNPY2R
SCHEMBL31688334	0.89	OPRD1 (0.57)	NPY4RNPY1RNPY5R
SCHEMBL23229948	0.88	NPY4R (0.60)	NPY4RNPY1RNPY5RNPY2RKISS1R
SCHEMBL31440171	0.88	NPY4R (0.58)	NPY4RNPY1RNPY5RNPY2RKISS1R
SCHEMBL18085020	0.87	NPY4R (0.68)	NPY4RNPY1RNPY5RNPY2R
SCHEMBL29637467	0.87	NPY4R (0.66)	NPY4RNPY1RNPY5RNPY2RKISS1R
SCHEMBL31332213	0.87	NPY4R (0.70)	NPY4RNPY1RNPY5RNPY2RKISS1R

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 1 patent. claimed = in the patent's claims; disclosed = body only.

Patent	Title	Assignee	Published	Priority	Filing	Country	Status
CN-103710393-B	Utilize the method preparing chiral alcohol containing small peptide class ionic liquid reaction system	JIANG University OF TECHNOLOGY (CN)	2016-03-09	—	—	CN	disclosed