SCHEMBL178592

SCHEMBL178592

O=C(O)C1NCC[C@@H]1O

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
SCHEMBL114870 1.00 — —
SCHEMBL7412 1.00 — —
SCHEMBL63812 1.00 — —
SCHEMBL2025245 1.00 — —
SCHEMBL8088 1.00 — —
SCHEMBL1256601 1.00 — —
SCHEMBL1364961 1.00 — —
SCHEMBL200242 1.00 — —
Hydrochloric Acid SCHEMBL23391535 0.98 SLC1A2 (0.58) —
Bicarbonate SCHEMBL5179753 0.98 SLC1A2 (0.58) —

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4076492-A1 PCSK9 ANTAGONIST COMPOUNDS Merck Sharp & Dohme LLC (US) 2022-10-26 — — EP disclosed
WO-2018236928-A1 HEPATITIS C VIRUS NS3/4A PROTEASE INHIBITORS UNIVERSITY OF MASSACHUSETTS (US) 2018-12-27 — — WO disclosed
EP-3226900-A1 IDENTIFICATION OF VSIG8 AS THE PUTATIVE VISTA RECEPTOR AND ITS USE THEREOF TO PRODUCE VISTA/VSIG8 MODULATORS Immunext, Inc. (US) 2017-10-11 — — EP disclosed
WO-2016090347-A1 IDENTIFICATION OF VSIG8 AS THE PUTATIVE VISTA RECEPTOR AND ITS USE THEREOF TO PRODUCE VISTA/VSIG8 MODULATORS IMMUNEXT, INC. (US) 2016-06-09 — — WO disclosed
US-9061959-B2 Method for manufacturing optically active menthol TAKASAGO INTERNATIONAL CORPORATION (JP) 2015-06-23 — — US disclosed
US-9000192-B2 Catalyst for asymmetric hydrogenation and method for manufacturing optically active carbonyl compound using the same TAKASAGO INTERNATIONAL CORPORATION (JP) 2015-04-07 — — US disclosed
EP-2675912-A1 METHOD FOR ASSAYING OGFOD1 ACTIVITY Isis Innovation Ltd (GB) 2013-12-25 — — EP disclosed
EP-2647616-A1 METHOD FOR MANUFACTURING OPTICALLY ACTIVE MENTHOL Takasago International Corporation (JP) 2013-10-09 — — EP disclosed
US-20130253228-A1 METHOD FOR MANUFACTURING OPTICALLY ACTIVE MENTHOL TAKASAGO INTERNATIONAL CORPORATION (JP) 2013-09-26 — — US disclosed
US-20130217895-A1 CATALYST FOR ASYMMETRIC HYDROGENATION AND METHOD FOR MANUFACTURING OPTICALLY ACTIVE CARBONYL COMPOUND USING THE SAME TAKASAGO INTERNATIONAL CORPORATION (JP) 2013-08-22 — — US disclosed
EP-1725542-A1 VLA-4 ANTAGONISTS Merck & Co., Inc. (US) 2006-11-29 — — EP disclosed
WO-2006115918-A2 VLA-4 ANTAGONISTS MERCK & CO., INC. (US) 2006-11-02 — — WO disclosed
WO-2006023396-A2 VLA-4 ANTAGONISTS MERCK & CO., INC. (US) 2006-03-02 — — WO disclosed
US-20050277167-A1 Prolyl 3-hydroxylases SHRINERS HOSPITALS FOR CHILDREN 2005-12-15 — — US disclosed
WO-2005112999-A2 CANCER TREATMENT WITH INHIBITORS OF COLLAGEN SYNTHESIS VECTRAMED, INC. (US) 2005-12-01 — — WO disclosed
WO-2005087760-A1 VLA-4 ANTAGONISTS MERCK & CO., INC. (US) 2005-09-22 — — WO disclosed
EP-1416932-A1 NEW DIPEPTIDYL PEPTIDASE IV INHIBITORS AND THEIR USES FOR LOWERING BLOOD PRESSURE LEVELS Probiodrug AG (DE) 2004-05-12 — — EP disclosed
WO-2003015775-A1 NEW DIPEPTIDYL PEPTIDASE IV INHIBITORS AND THEIR USES FOR LOWERING BLOOD PRESSURE LEVELS PROBIODRUG AG (DE) 2003-02-27 — — WO disclosed
EP-1014945-A1 CATIONIC LIPID COMPOSITIONS TARGETING ANGIOGENIC ENDOTHELIAL CELLS The Regents of the University of California (US) 2000-07-05 — — EP disclosed
WO-1998040052-A1 CATIONIC LIPID COMPOSITIONS TARGETING ANGIOGENIC ENDOTHELIAL CELLS THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 1998-09-17 — — WO disclosed
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