SCHEMBL458049

SCHEMBL458049

C/C=C\CC(N)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
SCHEMBL458050 1.00 — —
SCHEMBL14388431 1.00 — —
SCHEMBL866068 1.00 — —
SCHEMBL8186028 1.00 — —
SCHEMBL8186027 1.00 — —
SCHEMBL13406449 1.00 — —
SCHEMBL15703578 1.00 — —
Hydrochloric Acid SCHEMBL74585 0.98 GRIK1 (0.66) —
Hydrochloric Acid SCHEMBL712566 0.98 GRIK1 (0.66) —
Hydrochloric Acid SCHEMBL713389 0.98 GRIK1 (0.66) —

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4071477-B1 COMPOSITIONS AND METHODS FOR DIAGNOSING LYME DISEASE AND FOR PREDICTING LYME DISEASE SPIROCHETE ELIMINATION AFTER TREATMENT QIAGEN SCIENCES LLC (US) 2026-01-21 — — EP disclosed
US-20240384267-A1 COMPOSITIONS AND METHODS FOR MULTIPLEX DECODING OF QUADRUPLET CODONS THE BROAD INSTITUTE, INC. 2024-11-21 — — US disclosed
US-20240361314-A1 COMPOSITIONS AND METHODS FOR DIAGNOSING LYME DISEASE AND FOR PREDICTING LYME DISEASE SPIROCHETE ELIMINATION AFTER TREATMENT QIAGEN SCIENCES LLC (US) 2024-10-31 — — US disclosed
US-20240294586-A1 TENASCIN-C AUTOANTIGENIC EPITOPES IN RHEUMATOID ARTHRITIS BENAROYA RES INSTITUTE AT VIRGINIA MASON (US) 2024-09-05 — — US disclosed
US-12066436-B2 Compositions and methods for diagnosing Lyme disease and for predicting Lyme disease spirochete elimination after treatment QIAGEN SCIENCES LLC (US) 2024-08-20 — — US disclosed
US-20240027450-A1 COMPOSITIONS AND METHODS FOR DIAGNOSING SARS-COV-2 (COVID-19) AND FOR MONITORING SARS-COV-2-SPECIFIC IMMUNOLOGICAL MEMORY QIAGEN SCIENCES LLC 2024-01-25 — — US disclosed
EP-4256334-A1 COMPOSITIONS AND METHODS FOR DIAGNOSING SARS-COV-2 (COVID-19) AND FOR MONITORING SARS-COV-2-SPECIFIC IMMUNOLOGICAL MEMORY Qiagen Sciences LLC (US) 2023-10-11 — — EP disclosed
WO-2023069816-A2 COMPOSITIONS AND METHODS FOR MULTIPLEX DECODING OF QUADRUPLET CODONS THE BROAD INSTITUTE, INC. (US) 2023-04-27 — — WO disclosed
EP-3353551-B1 COMPOSITIONS AND METHODS FOR DIAGNOSING LYME DISEASE AND FOR PREDICTING LYME DISEASE SPIROCHETE ELIMINATION AFTER TREATMENT QIAGEN SCIENCES LLC (US) 2022-11-02 — — EP disclosed
EP-4071477-A1 COMPOSITIONS AND METHODS FOR DIAGNOSING LYME DISEASE AND FOR PREDICTING LYME DISEASE SPIROCHETE ELIMINATION AFTER TREATMENT QIAGEN Sciences, LLC (US) 2022-10-12 — — EP disclosed
US-20080026422-A1 Adding an desired amino acid analog to a medium containing a host cell with a vector coding for aminoacyl-tRNA synthetase and a vector coding for the polypeptide of interest; and growing the cell to produce the modified polypeptide CALIFORNIA INSTITUTE OF TECHNOLOGY (US) 2008-01-31 — — US disclosed
WO-2008005531-A2 C-MET RECEPTOR REGULATION BY ANGIOTENSIN IV (AT4) RECEPTOR LIGANDS WASHINGTON STATE UNIVERSITY RESEARCH FOUNDATION (US) 2008-01-10 — — WO disclosed
US-20080008701-A1 C-MET RECEPTOR REGULATION BY ANGIOTENSIN IV (AT4) RECEPTOR LIGANDS WASHINGTON STATE UNIVERSITY RESEARCH FOUNDATION (US) 2008-01-10 — — US disclosed
WO-2007130453-A2 NON-NATURAL AMINO ACID SUBSTITUTED POLYPEPTIDES ALLOZYNE, INC. (US) 2007-11-15 — — WO disclosed
WO-2007103307-A2 SITE-SPECIFIC INCORPORATION OF AMINO ACIDS INTO MOLECULES CALIFORNIA INSTITUTE OF TECHNOLOGY (US) 2007-09-13 — — WO disclosed
US-7198915-B2 Preparing modified/artificial polypeptides; mimetics CALIFORNIA INSTITUTE OF TECHNOLOGY (US) 2007-04-03 — — US disclosed
US-7198915-B2 Preparing modified/artificial polypeptides; mimetics CALIFORNIA INSTITUTE OF TECHNOLOGY (US) 2007-04-03 — — US disclosed
US-20040058415-A1 Preparing modified/artificial polypeptides; mimetics CALIFORNIA INSTITUTE OF TECHNOLOGY 2004-03-25 — — US disclosed
US-6586207-B2 Host cell is a methionine auxotroph; methionine-tRNA synthetase overexpressed in presence of analogues and absence of methionine; protein is modified dihydrofolate reductase CALIFORNIA INSTITUTE OF TECHNOLOGY 2003-07-01 — — US disclosed
US-20020042097-A1 Host cell is a methionine auxotroph; methionine-tRNA synthetase overexpressed in presence of analogues and absence of methionine; protein is modified dihydrofolate reductase CALIFORNIA INSTITUTE OF TECHNOLOGY 2002-04-11 — — US disclosed
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