SCHEMBL9108425

SCHEMBL9108425

Cc1cnccc1-n1c(C)cccc1=O

nearest known ligand 0.36

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ CA12 O43570 2/20 0.36
▸ CA1 P00915 2/20 0.36
▸ CA2 P00918 2/20 0.36
▸ CA9 Q16790 2/20 0.36
▸ CA14 Q9ULX7 1/20 0.36
▸ OPRM1 P35372 1/20 0.36
▸ OPRL1 P41146 1/20 0.36
▸ IDO1 P14902 2/20 0.34
▸ CHRM1 P11229 1/20 0.34
▸ TRPA1 O75762 1/20 0.33
▸ CCR9 P51686 1/20 0.32
▸ P2RX7 Q99572 1/20 0.32
▸ TDP1 Q9NUW8 2/20 0.32
▸ SIRT3 Q9NTG7 1/20 0.32
▸ CYP1A2 P05177 1/20 0.32
▸ CYP3A4 P08684 1/20 0.32
▸ TGFBR1 P36897 1/20 0.32
▸ KDM4E B2RXH2 1/20 0.32
▸ MAPT P10636 1/20 0.32
▸ GRM4 Q14833 1/20 0.31

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
SCHEMBL30854442 0.78 P2RX7 (0.33) CA12CA1CA2CA9CA14
SCHEMBL17809517 0.78 IDO1 (0.35) CA12CA1CA2CA9OPRM1
SCHEMBL31381659 0.77 CYP1A2 (0.40) OPRM1OPRL1CYP1A2CYP3A4TGFBR1
SCHEMBL31419562 0.76 CYP2A6 (0.50) CA12CA1CA2CA9TDP1
SCHEMBL9113104 0.75 GSR (0.41) KDM4EMAPTNPSR1KMT2A
SCHEMBL30527437 0.73 CA12 (0.60) CA12CA1CA2CA9CA14
SCHEMBL30854385 0.71 MYC (0.45) IDO1CCR9P2RX7KDM4EMAPT
SCHEMBL31419628 0.71 KDM5B (0.39) OPRM1OPRL1TDP1CYP1A2CYP3A4
SCHEMBL31419636 0.71 KCNJ5 (0.32) GRM4
SCHEMBL30555542 0.70 MYC (0.39) TDP1KDM4EMAPTMYCNR4A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4125891-A1 PROCESS, COMPOSITIONS, AND CRYSTALLINE FORMS OF SUBSTITUTED PYRIDINONE-PYRIDINYL COMPOUNDS Aclaris Therapeutics, Inc. (US) 2023-02-08 — — EP claimed
EP-4735431-A2 MK2 INHIBITORS AND METHODS OF MAKING AND USING THE SAME GILEAD SCIENCES, INC. (US) 2026-05-06 — — EP disclosed
US-12616696-B2 Crystalline forms of (p)-3-chloro-4-((3,5-difluoropyridin-2-yl)methoxy)-2′-(2-(2-hydroxypropan-2-yl)pyrimidin-4-yl)-5′,6-dimethyl-2h-[1,4′-bipyridin]-2-one ACLARIS THERAPEUTICS, INC. (US) 2026-05-05 — — US disclosed
US-12545662-B2 MK2 inhibitors and uses thereof XINTHERA, INC. (US) 2026-02-10 — — US disclosed
US-20250051309-A1 MK2 INHIBITORS AND METHODS OF MAKING AND USING THE SAME GILEAD SCIENCES, INC. 2025-02-13 — — US disclosed
WO-2025006568-A2 MK2 INHIBITORS AND METHODS OF MAKING AND USING THE SAME GILEAD SCIENCES, INC. (US) 2025-01-02 — — WO disclosed
CN-118510776-A Five-membered ring-containing derivative, preparation method and application thereof 上海翰森生物医药科技有限公司 2024-08-16 — — CN disclosed
CN-116178345-B Substituted pyrimidinyl-pyridinyl-pyridone compound, and preparation method and application thereof 深圳信立泰药业股份有限公司 2024-08-13 — — CN disclosed
EP-4367099-A1 PYRIDINONE MK2 INHIBITORS AND USES THEREOF Xinthera, Inc. (US) 2024-05-15 — — EP disclosed
WO-2024046327-A1 P38α-MK2 INHIBITOR COMPOUNDS, PHARMACEUTICAL COMPOSITIONS, AND USE THEREOF 长春金赛药业有限责任公司 2024-03-07 — — WO disclosed
CN-116178345-A Substituted pyrimidinyl-pyridinyl-pyridone compound, and preparation method and application thereof 深圳信立泰药业股份有限公司 2023-05-30 — — CN disclosed
EP-4125891-A1 PROCESS, COMPOSITIONS, AND CRYSTALLINE FORMS OF SUBSTITUTED PYRIDINONE-PYRIDINYL COMPOUNDS Aclaris Therapeutics, Inc. (US) 2023-02-08 — — EP disclosed
WO-2023283338-A1 PYRIDINONE MK2 INHIBITORS AND USES THEREOF XINTHERA, INC. (US) 2023-01-12 — — WO disclosed
US-9365546-B2 Substituted pyridinone-pyridinyl compounds CONFLUENCE LIFE SCIENCES INC. (US) 2016-06-14 — — US disclosed
US-9365547-B2 Substituted pyridinone-pyridinyl compounds CONFLUENCE LIFE SCIENCES INC. (US) 2016-06-14 — — US disclosed
US-20140171449-A1 SUBSTITUTED PYRIDINONE-PYRIDINYL COMPOUNDS CONFLUENCE LIFE SCIENCES INC. (US) 2014-06-19 — — US disclosed
US-20140171450-A1 SUBSTITUTED PYRIDINONE-PYRIDINYL COMPOUNDS CONFLUENCE LIFE SCIENCES INC. (US) 2014-06-19 — — US disclosed
EP-2648516-A1 SUBSTITUTED PYRIDINONE-PYRIDINYL COMPOUNDS Confluence Life Sciences, Inc. (US) 2013-10-16 — — EP disclosed
WO-2012078684-A1 SUBSTITUTED PYRIDINONE-PYRIDINYL COMPOUNDS CONFLUENCE LIFE SCIENCES, INC. (US) 2012-06-14 — — WO disclosed
US-20120142709-A1 SUBSTITUTED PYRIDINONE-PYRIDINYL COMPOUNDS ACLARIS THERAPEUTICS, INC. 2012-06-07 — — 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-20140171450-A1 SUBSTITUTED PYRIDINONE-PYRIDINYL COMPOUNDS MAPK1, MAP3K1, MAP3K6 CA12 4878/4885CA1 4867/4885CA2 4778/4885
US-20250051309-A1 MK2 INHIBITORS AND METHODS OF MAKING AND USING THE SAME DUSP2, MKNK2, DUSP22 CA12 2924/4885CA1 2854/4885CA2 1573/4885
US-20120142709-A1 SUBSTITUTED PYRIDINONE-PYRIDINYL COMPOUNDS MAPK1, MAP3K1, MAP3K6 CA12 4878/4885CA1 4867/4885CA2 4778/4885
US-12616696-B2 Crystalline forms of (p)-3-chloro-4-((3,5-difluoropyridin-2-yl)methoxy)-2′-(2-(2-hydroxypropan-2-yl)pyrimidin-4-yl)-5′,6-dimethyl-2h-[1,4′-bipyridin]-2-one MALT1, SSB, BCL9 CA12 2565/4885CA1 1709/4885CA2 2220/4885
US-12545662-B2 MK2 inhibitors and uses thereof NR3C2, NR2C2, AGTR2 CA12 2601/4885CA1 3101/4885CA2 1270/4885
US-20140171449-A1 SUBSTITUTED PYRIDINONE-PYRIDINYL COMPOUNDS MAPK1, MAP3K1, MAP3K6 CA12 4878/4885CA1 4867/4885CA2 4778/4885

“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.

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