SCHEMBL8610401

SCHEMBL8610401

OCC1(CO)CCOC1

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
SCHEMBL24045299 0.85
SCHEMBL29821784 0.85
SCHEMBL26049463 0.85
SCHEMBL24485365 0.85
SCHEMBL29017392 0.85
SCHEMBL8607807 0.84 EPHX1 (0.39)
SCHEMBL3301796 0.82 EPHX1 (0.39)
SCHEMBL30782062 0.80 EPHX1 (0.32)
SCHEMBL9516701 0.80 EPHX1 (0.43)
SCHEMBL1239755 0.76 EPHX1 (0.35)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2025111582-A1 AZA-TETRACYCLIC OXAZEPINE INHIBITORS OF KRAS-G12D GENENTECH, INC. (US) 2025-05-30 WO disclosed
US-20240140957-A1 BRIDGED COMPOUNDS AS KRAS G12D INHIBITOR AND DEGRADER AND THE USE THEREOF BEONE MEDICINES I GMBH (CH) 2024-05-02 US disclosed
WO-2022148422-A1 BRIDGED COMPOUNDS AS KRAS G12D INHIBITOR AND DEGRADER AND THE USE THEREOF BEIGENE, LTD. (KY) 2022-07-14 WO disclosed
CN-112778507-B Preparation method of hydrolysis-resistant hyperbranched polycaprolactone 山东一诺威新材料有限公司 2022-06-07 CN disclosed
EP-2794596-B1 SUBSTITUTED BENZYLPYRAZOLES BAYER IP GMBH (DE) 2017-05-31 EP disclosed
US-5821391-A HYDROGENATING 1,3-DIOXANES IN THE PRESENCE OF A CATALYST HOECHST AKTIENGESELLSCHAFT (DE) 1998-10-13 US disclosed
US-5780686-A REACTING 1,3-DIOXANES WITH AMMONIA AND HYDROGEN IN PRESENCE OF HYDROGENATION CATALYST HOECHST AKTIENGESELLSCHAFT (DE) 1998-07-14 US disclosed
US-5780687-A REACTING 1,3-DIOXANES WITH HYDROGEN IN PRESENCE OF HYDROGENATION CATALYST HOECHST AKTIENGESELLSCHAFT (DE) 1998-07-14 US disclosed
EP-0810194-A1 Process for preparing 3-oxyalkylpropan-1-ols HOECHST AKTIENGESELLSCHAFT (DE) 1997-12-03 EP disclosed
EP-0810202-A2 Process for the preparation of 4-oxaamines HOECHST AKTIENGESELLSCHAFT (DE) 1997-12-03 EP disclosed
EP-0291806-B1 TRANSFORMATION OF 1,3-DIOXANES INTO 4-OXA-ALDEHYDES BASF Aktiengesellschaft (DE) 1992-08-26 EP disclosed
EP-0291807-B1 TRANSFORMATION OF 1,3-DIOXANES INTO 4-OXA-ALDEHYDES BASF Aktiengesellschaft (DE) 1992-01-15 EP disclosed
EP-0199210-B1 CONVERSION OF 1,3-DIOXANES INTO 4-OXA-ALDEHYDES BASF Aktiengesellschaft (DE) 1991-10-16 EP disclosed
US-5012005-A Catalytic isomerization using a metal oxide catalyst BASF AKTIENGESELLSCHAFT (DE) 1991-04-30 US disclosed
US-4939280-A Aluminum phosphate catalysts with zeolitic structure molcular sieves BASF AKTIENGESELLSCHAFT (DE) 1990-07-03 US disclosed
EP-0291807-A1 Transformation of 1,3-dioxanes into 4-oxa-aldehydes BASF Aktiengesellschaft (DE) 1988-11-23 EP disclosed
EP-0291806-A1 Transformation of 1,3-dioxanes into 4-oxa-aldehydes BASF Aktiengesellschaft (DE) 1988-11-23 EP disclosed
US-4709097-A CATALYTIC ISOMERIZATION WITH ACIDIC ZEOLITE BASF AKTIENGESELLSCHAFT (DE) 1987-11-24 US disclosed
EP-0199210-A2 Conversion of 1,3-dioxanes into 4-oxa-aldehydes BASF Aktiengesellschaft (DE) 1986-10-29 EP disclosed