SCHEMBL28210612

SCHEMBL28210612

C[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(N)=O)NC(=O)[C@H](CS)NC(=O)[C@H](CS)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CS)NC(=O)[C@@H](N)CS)C(=O)N[C@@H](CS)C(=O)N[C@H](C(=O)NCC(=O)N[C@@H](CS)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)O)[C@@H](C)O

nearest known ligand 0.57

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
▸ OPRM1 P35372 4/20 0.55
▸ OPRD1 P41143 4/20 0.55
▸ OPRK1 P41145 2/20 0.55
▸ KEAP1 Q14145 1/20 0.55
▸ SLC6A2 P23975 1/20 0.54
▸ CALCR P30988 5/20 0.53
▸ RAMP3 O60896 1/20 0.51
▸ MAPK8 P45983 1/20 0.50
▸ MAPK9 P45984 1/20 0.50
▸ MAPK10 P53779 1/20 0.50
▸ HCRTR1 O43613 1/20 0.50
▸ HCRTR2 O43614 1/20 0.50

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
SCHEMBL15130591 1.00 OPRM1 (0.55) OPRM1OPRD1OPRK1KEAP1SLC6A2
SCHEMBL30163263 1.00 OPRM1 (0.55) OPRM1OPRD1OPRK1KEAP1SLC6A2
SCHEMBL14549930 1.00 OPRM1 (0.55) OPRM1OPRD1OPRK1KEAP1SLC6A2
SCHEMBL28846618 1.00 OPRM1 (0.55) OPRM1OPRD1OPRK1KEAP1SLC6A2
SCHEMBL30163405 0.99 OPRM1 (0.56) OPRM1OPRD1OPRK1KEAP1SLC6A2
SCHEMBL30163248 0.99 OPRM1 (0.55) OPRM1OPRD1OPRK1KEAP1SLC6A2
SCHEMBL29597272 0.98 OPRM1 (0.55) OPRM1OPRD1OPRK1KEAP1SLC6A2
SCHEMBL14549924 0.97 KEAP1 (0.56) OPRM1OPRD1OPRK1KEAP1SLC6A2
SCHEMBL11997748 0.97 KEAP1 (0.56) OPRM1OPRD1OPRK1KEAP1SLC6A2
SCHEMBL30163250 0.97 KEAP1 (0.56) OPRM1OPRD1OPRK1KEAP1SLC6A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3846788-B1 PDE11 INHIBITORS FOR USE FOR THE TREATMENT OF PARKINSON'S DISEASE UNIV AMSTERDAM (NL) 2025-10-29 — — EP disclosed
EP-4606386-A2 SPECIFIC INCREASE OF DOPAMINE SYNTHESIS THROUGH TARGETING OF THE GUANYLATE CYCLASE 2C RECEPTOR IN THE TREATMENT OF PARKINSON S DISEASE Universiteit van Amsterdam (NL) 2025-08-27 — — EP disclosed
EP-3589305-B1 SPECIFIC INCREASE OF DOPAMINE SYNTHESIS THROUGH TARGETING OF THE GUANYLATE CYCLASE 2C RECEPTOR IN THE TREATMENT OF PARKINSON'S DISEASE UNIV AMSTERDAM (NL) 2025-07-02 — — EP disclosed
CN-114195855-B Solid phase synthesis method for polypeptide containing three pairs of disulfide bonds by introducing one pair of disulfide bonds 深圳翰宇药业股份有限公司 2025-01-24 — — CN disclosed
CN-118359685-A Preparation method of linaclotide 成都倍特药业股份有限公司 2024-07-19 — — CN disclosed
CN-117530912-A Stable solid formulations of guanylate cyclase-C receptor agonist polypeptides suitable for oral administration 硬木药品公司 2024-02-09 — — CN disclosed
CN-114195855-A Solid-phase synthesis method for polypeptide containing three pairs of disulfide bonds by introducing one pair of disulfide bonds 深圳翰宇药业股份有限公司 2022-03-18 — — CN disclosed
CN-107936094-A The synthetic method that a kind of solid liquid phase of Li Laluo peptides is combined 江苏诺泰澳赛诺生物制药股份有限公司 2018-04-20 — — CN disclosed
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