SCHEMBL462863

SCHEMBL462863

OCC1CCNCC1O

nearest known ligand 0.00

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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
SCHEMBL462864 1.00 — —
SCHEMBL29716692 1.00 — —
SCHEMBL505752 1.00 — —
SCHEMBL1313595 1.00 — —
SCHEMBL505465 1.00 — —
SCHEMBL505753 1.00 — —
Hydrochloric Acid SCHEMBL2919351 0.98 GBA1 (0.50) —
Hydrochloric Acid SCHEMBL2919348 0.98 GBA1 (0.50) —
Hydrochloric Acid SCHEMBL2919353 0.98 GBA1 (0.50) —
Hydrochloric Acid SCHEMBL2922089 0.98 GBA1 (0.50) —

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 184 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114685560-B Synthesis and application of phosphoramidite monomer containing piperidine skeleton and oligonucleotide 沈阳药科大学 2024-05-14 — — CN claimed
WO-2023088291-A1 AROMATIC AMINE COMPOUND AND APPLICATION THEREOF 武汉众诚康健生物医药科技有限公司 2023-05-25 — — WO claimed
CN-116135851-A Aromatic amine compound and application thereof 武汉众诚康健生物医药科技有限公司 2023-05-19 — — CN claimed
CN-114685560-A Synthesis and application of phosphoramidite monomer containing piperidine skeleton and oligonucleotide 沈阳药科大学 2022-07-01 — — CN claimed
CN-101381341-A Preparation method of 3-hydroxy-6-hydroxymethyl pyridine HUBEI ZHICHENG CHEMICAL TECHNO (CN) 2009-03-11 — — CN claimed
CN-1087367-A Structural adhesive composition with high temperature resistance LORD CORP (US) 1994-06-01 — — CN claimed
CN-122011024-A Phosphoramidite monomer containing bio-orthogonal groups and preparation method and application thereof 沈阳药科大学 2026-05-12 — — CN disclosed
US-20240308989-A1 PYRAN DERIVATIVES AS CYP11A1 (CYTOCHROME P450 MONOOXYGENASE 11A1) INHIBITORS ORION CORP (FI) 2024-09-19 — — US disclosed
US-12030871-B2 Pyran dervatives as CYP11A1 (cytochrome P450 monooxygenase 11A1) inhibitors ORION CORPORATION (FI) 2024-07-09 — — US disclosed
US-11999753-B2 Tetrahydropyridopyrimidine pan-KRas inhibitors Mirati Therapeutics, Inc. (US) 2024-06-04 — — US disclosed
CN-114685560-B Synthesis and application of phosphoramidite monomer containing piperidine skeleton and oligonucleotide 沈阳药科大学 2024-05-14 — — CN disclosed
CN-114685560-B Synthesis and application of phosphoramidite monomer containing piperidine skeleton and oligonucleotide 沈阳药科大学 2024-05-14 — — CN disclosed
CN-114728170-B Compounds active on nuclear receptors 纽韦卢森公司 2024-03-01 — — CN disclosed
CN-1015462-B METHOD FOR PREPARING 6-(SUBSTD.) METHYLENEPENICILLANIC ACIDS OR 1,1-DIOXIDE AND DERIVATIVES THEREOF PFIZER (US) 1992-02-12 — — CN disclosed
CN-1011788-B 6- (substituted) methylenepenicillanic acids and derivatives thereof PFIZER (US) 1991-02-27 — — CN disclosed
CN-1046905-A 6-(replacement) methylene radical penam acids; The method for making of 6-(replacement) methylol penicillin alkanoic acid class and derivative thereof PFIZER (US) 1990-11-14 — — CN disclosed
CN-1045788-A 6-(replacement) methylene radical penam acids; The method for making of 6-(replacement) methylol penicillin alkanoic acid class and derivative thereof PFIZER (US) 1990-10-03 — — CN disclosed
CN-1045789-A 6-(replacement) methylene radical penam acids; The method for making of 6-(replacement) methylol penam acids and derivative thereof PFIZER (US) 1990-10-03 — — CN disclosed
CN-1045787-A The method for making of 6-(replacement) methylene radical penam acids, 6-(replacement) methylol penam acids and derivative thereof PFIZER (US) 1990-10-03 — — CN disclosed
CN-85101572-A Process for producing 6- (substituted) methylenepenicillanic acids, 6- (substituted) hydroxymethylpenicillanic acids and derivatives thereof — 1986-10-29 — — CN disclosed
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