SCHEMBL1423019

SCHEMBL1423019

O=C(O)c1cc2n(n1)CCC2

nearest known ligand 0.48

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
HTR2A P28223 1/20 0.40
HTR2C P28335 1/20 0.40
PDK1 Q15118 1/20 0.38
PDK2 Q15119 1/20 0.38
LDHA P00338 1/20 0.37
ALOX15 P16050 1/20 0.36
TSHR P16473 1/20 0.36
HIF1A Q16665 1/20 0.36

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
SCHEMBL1423651 0.95 HTR2A (0.44) HTR2AHTR2CLDHA
SCHEMBL28517075 0.93 HTR2A (0.44) HTR2AHTR2CLDHA
Potassium Ion SCHEMBL5123542 0.82 HTR2A (0.39) HTR2AHTR2CPDK1PDK2LDHA
SCHEMBL22518543 0.80 HTR2A (0.40) HTR2AHTR2CPDK1PDK2LDHA
SCHEMBL24811454 0.78 HDAC6 (0.38) HTR2AHTR2CPDK1PDK2
SCHEMBL22831695 0.78 PDCD1 (0.36) TSHR
SCHEMBL1008113 0.77 CYP1A2 (0.48) ALOX15TSHRHIF1A
SCHEMBL20228734 0.77 HTR2A (0.38) HTR2AHTR2CPDK1PDK2LDHA
SCHEMBL22275219 0.75 ALDH1A1 (0.43) HTR2AHTR2CLDHA
SCHEMBL25485602 0.75 HTR2A (0.44) HTR2AHTR2CPDK1PDK2LDHA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20080009634-A1 Process for synthesizing beta-lactamase inhibitor intermediates WYETH HOLDINGS CORPORATION (US) 2008-01-10 US claimed
CN-1823074-A Process for synthesizing beta-lactamase inhibitor intermediates WYETH CORP (US) 2006-08-23 CN claimed
EP-1626975-A2 PROCESS FOR SYNTHESIZING ß-LACTAMASE INHIBITOR IN INTERMEDIATES Wyeth Holdings Corporation (US) 2006-02-22 EP claimed
WO-2004104006-A2 PROCESS FOR SYNTHESIZING β-LACTAMASE INHIBITOR IN INTERMEDIATES WYETH HOLDINGS CORPORATION (US) 2004-12-02 WO claimed
US-20040242874-A1 Process for synthesizing beta-lactamase inhibitor intermediates WYETH HOLDINGS CORPORATION 2004-12-02 US claimed
US-20260125346-A1 Isoquinolinone Derivatives and 4H-Quinolizinone Derivatives and Pharmaceutical Compositions Thereof for the Treatment of Disease BEONE MEDICINES I GMBH (CH) 2026-05-07 US disclosed
EP-4709711-A1 ISOQUINOLINONE DERIVATIVES AND 4H-QUINOLIZINONE DERIVATIVES AND PHARMACEUTICAL COMPOSITIONS THEREOF FOR THE TREATMENT OF DISEASE Beone Medicines I GmbH (CH) 2026-03-18 EP disclosed
EP-4688154-A1 MORPHOLINE OREXIN RECEPTOR ANTAGONISTS BIAL - Portela & Ca., S.A. (PT) 2026-02-11 EP disclosed
EP-4688155-A1 MORPHOLINE OREXIN RECEPTOR ANTAGONISTS Bial-Portela & CA, S.A. (PT) 2026-02-11 EP disclosed
US-12459951-B2 Compounds that interact with RAS superfamily proteins for treatment of cancers, inflammatory diseases, rasopathies, and fibrotic disease SHY THERAPEUTICS, LLC (US) 2025-11-04 US disclosed
CN-120058672-A Halogenated pyridylcarboxylic acid ester derivative and application thereof 贵州医科大学 2025-05-30 CN disclosed
US-20250154134-A1 COMPOUND AS FAK INHIBITOR AND USE THEREOF Wigen Biomedicine Technology (shanghai) Co., Ltd. (CN) 2025-05-15 US disclosed
CN-1823069-A Process for synthesizing beta-lactamase inhibitor intermediates WYETH CORP (US) 2006-08-23 CN disclosed
EP-1626972-A1 PROCESS FOR SYNTHESIZING ß-LACTAMASE INHIBITOR INTERMEDIATES Wyeth Holdings Corporation (US) 2006-02-22 EP disclosed
EP-1626975-A2 PROCESS FOR SYNTHESIZING ß-LACTAMASE INHIBITOR IN INTERMEDIATES Wyeth Holdings Corporation (US) 2006-02-22 EP disclosed
CN-1649883-A Bicyclic 6-alkylidene-epimycotenes as lactamase inhibitors WYETH CORP (US) 2005-08-03 CN disclosed
WO-2004104006-A2 PROCESS FOR SYNTHESIZING β-LACTAMASE INHIBITOR IN INTERMEDIATES WYETH HOLDINGS CORPORATION (US) 2004-12-02 WO disclosed
WO-2004104008-A1 PROCESS FOR SYNTHESIZING β-LACTAMASE INHIBITOR INTERMEDIATES WYETH HOLDINGS CORPORATION (US) 2004-12-02 WO disclosed
US-20040242874-A1 Process for synthesizing beta-lactamase inhibitor intermediates WYETH HOLDINGS CORPORATION 2004-12-02 US disclosed
US-20040229324-A1 Production of bicyclic-heteroaryl-2-carboxylic acids by selective enzymatic hydrolysis of a mixture of positional esters WYETH HOLDINGS CORPORATION 2004-11-18 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (6 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20080009634-A1 Process for synthesizing beta-lactamase inhibitor intermediates COASY, DCXR, MGAM HTR2A 3395/4885HTR2C 3603/4885PDK1 1267/4885
US-20040229324-A1 Production of bicyclic-heteroaryl-2-carboxylic acids by selective enzymatic hydrolysis of a mixture of positional esters COASY, CES2, CES1 HTR2A 3771/4885HTR2C 3650/4885PDK1 833/4885
US-12459951-B2 Compounds that interact with RAS superfamily proteins for treatment of cancers, inflammatory diseases, rasopathies, and fibrotic disease KRAS, HRAS, NRAS HTR2A 4770/4885HTR2C 4822/4885PDK1 2943/4885
US-20040242874-A1 Process for synthesizing beta-lactamase inhibitor intermediates COASY, DCXR, MGAM HTR2A 3362/4885HTR2C 3537/4885PDK1 1224/4885
US-20260125346-A1 Isoquinolinone Derivatives and 4H-Quinolizinone Derivatives and Pharmaceutical Compositions Thereof for the Treatment of Disease NR3C1, NR3C2, PIK3R4 HTR2A 261/4885HTR2C 325/4885PDK1 544/4885
US-20250154134-A1 COMPOUND AS FAK INHIBITOR AND USE THEREOF PTK2, PAK1, FYN HTR2A 4185/4885HTR2C 3867/4885PDK1 392/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.