Ramelteon

Ramelteon

SCHEMBL29380213

CCC(=O)NCC[C@@H]1CCc2ccc3c(c21)CCO3

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

MTNR1AMTNR1B

The experimentally established mechanism targets of Ramelteon. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 6)

geneUniProtsupporting neighboursconfidence
MTNR1A known ✓ P48039 20/20 1.00
MTNR1B known ✓ P49286 20/20 1.00
ABCB11 O95342 1/20 1.00
SIGMAR1 Q99720 1/20 1.00
USP2 O75604 1/20 1.00
NQO2 P16083 1/20 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.

Compoundsimilaritytop predictedshared targets
(R)-Ramelteon SCHEMBL1566122 1.00 MTNR1A (1.00) MTNR1AMTNR1BABCB11SIGMAR1USP2
Ramelteon SCHEMBL29237 1.00 MTNR1A (1.00) MTNR1AMTNR1BABCB11SIGMAR1USP2
(R)-Ramelteon SCHEMBL29827337 1.00 MTNR1A (1.00) MTNR1AMTNR1BABCB11SIGMAR1USP2
(R)-Ramelteon SCHEMBL338730 1.00 MTNR1A (1.00) MTNR1AMTNR1BABCB11SIGMAR1USP2
SCHEMBL1566589 0.91 MTNR1A (1.00) MTNR1AMTNR1BABCB11SIGMAR1USP2
SCHEMBL1567007 0.88 MTNR1A (1.00) MTNR1AMTNR1BABCB11SIGMAR1USP2
SCHEMBL1567415 0.88 MTNR1A (1.00) MTNR1AMTNR1BABCB11SIGMAR1USP2
SCHEMBL3065294 0.87 MTNR1A (1.00) MTNR1AMTNR1BABCB11SIGMAR1USP2
SCHEMBL13985044 0.86 MTNR1A (0.76) MTNR1AMTNR1BABCB11SIGMAR1USP2
SCHEMBL1612991 0.85 MTNR1A (0.78) MTNR1AMTNR1BABCB11SIGMAR1USP2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119950417-A Rametidine liquid preparation and preparation method and application thereof 湖南慧泽生物医药科技有限公司 2025-05-09 CN disclosed
CN-119775240-A Rametidine in Process for the preparation of intermediates 广东赛烽医药科技有限公司 2025-04-08 CN disclosed
WO-2025041809-A1 METHOD FOR PRODUCING DEUTERATED COMPOUND 国立大学法人九州大学 2025-02-27 WO disclosed
CN-118546047-B Preparation method of cyclic chiral nitrile compound and application of cyclic chiral nitrile compound in preparation of ramelteon 北京师范大学 2025-02-07 CN disclosed
EP-4502609-A2 DETERMINING A CIRCADIAN RHYTHM Vanda Pharmaceuticals Inc. (US) 2025-02-05 EP disclosed
CN-118546047-A Preparation method of cyclic chiral nitrile compound and application of cyclic chiral nitrile compound in preparation of ramelteon 北京师范大学 2024-08-27 CN disclosed
CN-118384118-A Ramelteon freeze-dried orally disintegrating tablet and preparation method thereof 广州国标检验检测有限公司 2024-07-26 CN disclosed
CN-117946050-A Preparation method of ramelteon impurity dimer 湖南慧泽生物医药科技有限公司 2024-04-30 CN disclosed
CN-117756760-A Synthesis method of 2, 3-dihydrobenzofuran 山东邹平大展新材料有限公司 2024-03-26 CN disclosed
WO-2023198882-A1 MELATONIN RECEPTOR AGONISTS FOR USE IN THE TREATMENT OF EPILEPSY DISORDERS THERACULE AS (NO) 2023-10-19 WO disclosed
CN-113045524-B Synthesis method of ramelteon intermediate 河南牧业经济学院 2023-09-22 CN disclosed
CN-115778925-A Ramelteon oral dissolving film agent and preparation method thereof 湖北广济医药科技有限公司 2023-03-14 CN disclosed
CN-115477628-A Synthesis method of ramelteon dimer 江苏海悦康医药科技有限公司 2022-12-16 CN disclosed
CN-110776485-B Preparation method of ramelteon impurity 山东邹平大展新材料有限公司 2022-09-30 CN disclosed
US-20220047608-A1 Method of Treatment and Pharmaceutical Composition for Morning Hypertension Dharma Laboratories LLC (US) 2022-02-17 US disclosed