2-Morpholinocyclohexanol

2-Morpholinocyclohexanol

SCHEMBL907957

OC1CCCCC1N1CCOCC1

nearest known ligand 0.63

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Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
▸ SLC18A3 Q16572 12/20 0.63
▸ CYP2D6 P10635 2/20 0.49
▸ TSHR P16473 2/20 0.49
▸ SMN1; SMN2 Q16637 2/20 0.49
▸ CYP1A2 P05177 1/20 0.49
▸ CYP2C9 P11712 1/20 0.49
▸ SIGMAR1 Q99720 1/20 0.49
▸ ALDH1A1 P00352 1/20 0.47
▸ APEX1 P27695 1/20 0.47
▸ BLM P54132 1/20 0.47

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
2-Morpholinocyclohexanol SCHEMBL908149 1.00 SLC18A3 (0.63) SLC18A3CYP2D6TSHRSMN1; SMN2CYP1A2
2-Morpholinocyclohexanol SCHEMBL6591797 1.00 SLC18A3 (0.63) SLC18A3CYP2D6TSHRSMN1; SMN2CYP1A2
2-Morpholinocyclohexanol SCHEMBL8989817 1.00 SLC18A3 (0.63) SLC18A3CYP2D6TSHRSMN1; SMN2CYP1A2
2-Morpholinocyclohexanol SCHEMBL12409428 1.00 SLC18A3 (0.63) SLC18A3CYP2D6TSHRSMN1; SMN2CYP1A2
SCHEMBL12014356 0.98 SLC18A3 (0.62) SLC18A3CYP2D6TSHRSMN1; SMN2CYP1A2
SCHEMBL12014352 0.98 SLC18A3 (0.62) SLC18A3CYP2D6TSHRSMN1; SMN2CYP1A2
SCHEMBL12014346 0.96 SLC18A3 (0.57) SLC18A3CYP2D6TSHRSMN1; SMN2CYP1A2
SCHEMBL12014347 0.86 SLC18A3 (0.45) SLC18A3CYP2D6TSHRSMN1; SMN2CYP1A2
SCHEMBL3969239 0.84 SLC18A3 (0.77) SLC18A3CYP2D6TSHRSMN1; SMN2CYP1A2
SCHEMBL25305403 0.81 SLC18A3 (0.74) SLC18A3CYP2D6TSHRSMN1; SMN2CYP1A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250179233-A1 PROCESS AND CATALYSTS FOR HYDROGEN MEDIATED ANIONIC COPOLYMERIZATION OF CONJUGATED DIENES AND LIQUID COPOLYMERS THEREOF ALBEMARLE CORPORATION (US) 2025-06-05 — — US claimed
EP-4486808-A2 PROCESS AND CATALYSTS FOR HYDROGEN MEDIATED ANIONIC COPOLYMERIZATION OF CONJUGATED DIENES AND LIQUID COPOLYMERS THEREOF ALBEMARLE CORPORATION (US) 2025-01-08 — — EP claimed
CN-119137172-A Process and catalyst for hydrogen-mediated anionic copolymerization of conjugated dienes and liquid copolymers thereof 雅宝公司 2024-12-13 — — CN claimed
US-20240034825-A1 PROCESS AND CATALYSTS FOR HYDROGEN MEDIATED ANIONIC POLYMERIZATION OF CONJUGATED DIENES AND LIQUID POLYMERS THEREOF ALBEMARLE CORPORATION 2024-02-01 — — US claimed
WO-2023168218-A2 PROCESS AND CATALYSTS FOR HYDROGEN MEDIATED ANIONIC COPOLYMERIZATION OF CONJUGATED DIENES AND LIQUID COPOLYMERS THEREOF ALBEMARLE CORPORATION (US) 2023-09-07 — — WO claimed
EP-4208485-A1 PROCESS AND CATALYSTS FOR HYDROGEN MEDIATED ANIONIC POLYMERIZATION OF CONJUGATED DIENES AND LIQUID POLYMERS THEREOF ALBEMARLE CORPORATION (US) 2023-07-12 — — EP claimed
CN-116368159-A Process and catalyst for hydrogen-mediated anionic polymerization of conjugated dienes and liquid polymers thereof 雅宝公司 2023-06-30 — — CN claimed
WO-2026107083-A2 SHELF-STABLE LOXSH CATALYST SOLUTION COMPOSITIONS COMPRISING SOLUBLE HIGH HYDRIDE CONCENTRATIONS AND THE PROCESSES FOR PREPARING THEM ALBEMARLE CORPORATION (US) 2026-05-21 — — WO disclosed
US-20250179233-A1 PROCESS AND CATALYSTS FOR HYDROGEN MEDIATED ANIONIC COPOLYMERIZATION OF CONJUGATED DIENES AND LIQUID COPOLYMERS THEREOF ALBEMARLE CORPORATION (US) 2025-06-05 — — US disclosed
EP-4486808-A2 PROCESS AND CATALYSTS FOR HYDROGEN MEDIATED ANIONIC COPOLYMERIZATION OF CONJUGATED DIENES AND LIQUID COPOLYMERS THEREOF ALBEMARLE CORPORATION (US) 2025-01-08 — — EP disclosed
CN-119137172-A Process and catalyst for hydrogen-mediated anionic copolymerization of conjugated dienes and liquid copolymers thereof 雅宝公司 2024-12-13 — — CN disclosed
US-20240034825-A1 PROCESS AND CATALYSTS FOR HYDROGEN MEDIATED ANIONIC POLYMERIZATION OF CONJUGATED DIENES AND LIQUID POLYMERS THEREOF ALBEMARLE CORPORATION 2024-02-01 — — US disclosed
WO-2023168218-A2 PROCESS AND CATALYSTS FOR HYDROGEN MEDIATED ANIONIC COPOLYMERIZATION OF CONJUGATED DIENES AND LIQUID COPOLYMERS THEREOF ALBEMARLE CORPORATION (US) 2023-09-07 — — WO disclosed
EP-0863755-A4 ANTITHROMBOTIC DIAMINES LILLY CO ELI (US) 1999-01-20 — — EP disclosed
EP-0863755-A1 ANTITHROMBOTIC DIAMINES ELI LILLY AND COMPANY (US) 1998-09-16 — — EP disclosed
WO-1997025033-A1 ANTITHROMBOTIC DIAMINES ELI LILLY AND COMPANY (US) 1997-07-17 — — WO disclosed
EP-0720605-A1 AMINOCYCLOHEXYLESTERS AND USES THEREOF UNIVERSITY OF BRITISH COLUMBIA (CA) 1996-07-10 — — EP disclosed
WO-1995008544-A1 AMINOCYCLOHEXYLESTERS AND USES THEREOF THE UNIVERSITY OF BRITISH COLUMBIA (CA) 1995-03-30 — — WO disclosed
EP-0632806-A1 AMINOCYCLOHEXYLAMIDES FOR ANTIARRHYTHMIC AND ANAESTHETIC USES. UNIV BRITISH COLUMBIA (CA) 1995-01-11 — — EP disclosed
WO-1993019056-A1 AMINOCYCLOHEXYLAMIDES FOR ANTIARRHYTHMIC AND ANAESTHETIC USES THE UNIVERSITY OF BRITISH COLUMBIA (CA) 1993-09-30 — — WO disclosed
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