SCHEMBL1006909

SCHEMBL1006909

O=[C]C(O)O

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
SCHEMBL720480 1.00
SCHEMBL10427686 0.74
SCHEMBL667678 0.74
SCHEMBL10427707 0.74
SCHEMBL3188225 0.74
SCHEMBL2726510 0.74
SCHEMBL61233 0.70
SCHEMBL4217446 0.70
SCHEMBL6425152 0.70
SCHEMBL1950819 0.70

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-1995016049-A1 CATALYTIC CHEMO-ENZYMATIC ASYMMETRIC SYNTHESIS OF CARBOHYDRATES THE SCRIPPS RESEARCH INSTITUTE (US) 1995-06-15 WO claimed
WO-1992010503-A1 PROCESS FOR THE PREPARATION OF 3,5-DIHYDROXY 6-OXO HEXANOIC ACID RHONE-POULENC RORER S.A. (FR) 1992-06-25 WO claimed
EP-0101598-B1 BETA-LACTAMS F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) 1988-04-20 EP claimed
EP-0101598-A1 Beta-lactams F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) 1984-02-29 EP claimed
CN-115043749-B Preparation method of diamide diol 东华大学 2023-06-27 CN disclosed
CN-115043749-A Preparation method of diamide diol 东华大学 2022-09-13 CN disclosed
CN-112638423-A Bioconjugates of neuropeptide derivatives 法国国家科学研究中心 2021-04-09 CN disclosed
US-20200262725-A1 SYSTEM AND METHOD FOR GENERATION OF REACTIVE OXYGEN SPECIES AND APPLICATIONS THEREOF PACIFIC WESTERN BANK D/B/A PACIFIC WESTERN BUSINESS FINANCE 2020-08-20 US disclosed
US-20170107128-A1 SYSTEM AND METHOD FOR GENERATION OF REACTIVE OXYGEN SPECIES AND APPLICATIONS THEREOF SILICON VALLEY BANK 2017-04-20 US disclosed
CN-104662085-B Polyvinyl acetal based resin composition SEKISUI CHEMICAL CO.,LTD. (JP) 2016-04-13 CN disclosed
EP-2892854-A1 SYSTEMS AND METHODS FOR GENERATION OF REACTIVE OXYGEN SPECIES AND APPLICATIONS THEREOF Clean Chemistry, LLC (US) 2015-07-15 EP disclosed
CN-104662085-A Polyvinyl acetal-based resin composition SEKISUI CHEMICAL CO LTD 2015-05-27 CN disclosed
WO-1992010503-A1 PROCESS FOR THE PREPARATION OF 3,5-DIHYDROXY 6-OXO HEXANOIC ACID RHONE-POULENC RORER S.A. (FR) 1992-06-25 WO disclosed
US-5041565-A Cardiovascular disorders HOECHST-ROUSSEL PHARMACEUTICALS INC. (US) 1991-08-20 US disclosed
US-4883793-A Hydrazinocarbonyloxylabdanes for treating cardiac failure HOECHST-ROUSSEL PHARMACEUTICALS INC. (US) 1989-11-28 US disclosed
EP-0341571-A1 Hydrazinocarbonyloxylabdanes, a process for their preparation and their use as medicaments HOECHST-ROUSSEL PHARMACEUTICALS INCORPORATED (US) 1989-11-15 EP disclosed
EP-0101598-B1 BETA-LACTAMS F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) 1988-04-20 EP disclosed
EP-0058097-B1 PROCESS FOR THE PREPARATION OF 17-ALPHA-HYDROXY-17-BETA-HYDROXYACETYL STEROIDS, AND CORRESPONDING INTERMEDIATES OBTAINED ROUSSEL-UCLAF (FR) 1984-07-25 EP disclosed
EP-0101598-A1 Beta-lactams F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) 1984-02-29 EP disclosed
EP-0058097-A2 Process for the preparation of 17-alpha-hydroxy-17-beta-hydroxyacetyl steroids, and corresponding intermediates obtained ROUSSEL-UCLAF (FR) 1982-08-18 EP disclosed