SCHEMBL23040246

SCHEMBL23040246

CCC(Cl)c1ccc(C(F)(F)F)cc1

nearest known ligand 0.46

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
▸ PDE2A O00408 2/20 0.46
▸ CES2 O00748 1/20 0.39
▸ CES1 P23141 1/20 0.39
▸ MC4R P32245 1/20 0.39
▸ ACP3 P15309 1/20 0.37
▸ FFAR1 O14842 3/20 0.36
▸ CNR2 P34972 1/20 0.36
▸ TAAR1 Q96RJ0 1/20 0.36
▸ ALDH1A1 P00352 1/20 0.36
▸ KIF11 P52732 1/20 0.36
▸ HSD11B1 P28845 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
SCHEMBL5607146 0.82 TDP1 (0.42) ALDH1A1
SCHEMBL10369500 0.81 GRIA4 (0.42) FFAR1KIF11
SCHEMBL28858449 0.79 CES2 (0.39) PDE2ACES2CES1ACP3CNR2
SCHEMBL14369491 0.78 PDE2A (0.48) PDE2ACES2CES1MC4RACP3
SCHEMBL13126259 0.78 PDE2A (0.48) PDE2ACES2CES1MC4RACP3
SCHEMBL4839555 0.77 KIF11 (0.43) PDE2AFFAR1KIF11
SCHEMBL28347282 0.77 PDE2A (0.52) PDE2ACES2CES1MC4RALDH1A1
SCHEMBL435755 0.77 PDE2A (0.52) PDE2ACES2CES1MC4RALDH1A1
SCHEMBL27528113 0.77 PDE2A (0.47) PDE2ACES2CES1MC4RACP3
SCHEMBL13622230 0.77 PDE2A (0.52) PDE2ACES2CES1MC4RALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4021901-B1 SUBSTITUTED PYRIDOPYRIMIDINONYL COMPOUNDS USEFUL AS T CELL ACTIVATORS BRISTOL MYERS SQUIBB CO (US) 2025-09-24 — — EP disclosed
EP-4583876-A1 COMBINATION OF A T CELL THERAPY AND CONTINUOUS OR INTERMITTENT DGK INHIBITOR DOSING Juno Therapeutics, Inc. (US) 2025-07-16 — — EP disclosed
CN-120152717-A Combination of T cell therapy and continuous or intermittent DGK inhibitor administration 朱诺治疗学股份有限公司 2025-06-13 — — CN disclosed
US-20240400563-A1 SUBSTITUTED PYRIDOPYRIMIDINONYL COMPOUNDS USEFUL AS T CELL ACTIVATORS BRISTOL-MYERS SQUIBB COMPANY 2024-12-05 — — US disclosed
CN-114302884-B Substituted pyridopyrimidinone compounds useful as T cell activators 百时美施贵宝公司 2024-06-04 — — CN disclosed
US-20240108654-A1 COMBINATION OF A T CELL THERAPY AND A DGK INHIBITOR JUNO THERAPEUTICS, INC. (US) 2024-04-04 — — US disclosed
WO-2024054944-A1 COMBINATION OF A T CELL THERAPY AND CONTINUOUS OR INTERMITTENT DGK INHIBITOR DOSING JUNO THERAPEUTICS, INC. (US) 2024-03-14 — — WO disclosed
CN-117693508-A Combination of T cell therapy and DGK inhibitors 朱诺治疗学股份有限公司 2024-03-12 — — CN disclosed
EP-4301755-A1 COMBINATION OF A T CELL THERAPY AND A DGK INHIBITOR Juno Therapeutics, Inc. (US) 2024-01-10 — — EP disclosed
WO-2023184327-A1 KINASE INHIBITORS, PREPARATION METHODS AND USES THEREOF InventisBio Co., Ltd. (CN) 2023-10-05 — — WO disclosed
US-20230089255-A1 COMBINATIONS OF DGK INHIBITORS AND CHECKPOINT ANTAGONISTS BRISTOL-MYERS SQUIBB COMPANY 2023-03-23 — — US disclosed
US-11584747-B2 Substituted pyridopyrimidinonyl compounds useful as T cell activators SYNGENE INTERNATIONAL LIMITED (IN) 2023-02-21 — — US disclosed
EP-4076529-A1 COMBINATIONS OF DGK INHIBITORS AND CHECKPOINT ANTAGONISTS Bristol-Myers Squibb Company (US) 2022-10-26 — — EP disclosed
CN-115243721-A Combination of DGK inhibitors and checkpoint antagonists 百时美施贵宝公司 2022-10-25 — — CN disclosed
WO-2022187406-A1 COMBINATION OF A T CELL THERAPY AND A DGK INHIBITOR JUNO THERAPEUTICS, INC. (US) 2022-09-09 — — WO disclosed
EP-4021901-A1 SUBSTITUTED PYRIDOPYRIMIDINONYL COMPOUNDS USEFUL AS T CELL ACTIVATORS Bristol-Myers Squibb Company (US) 2022-07-06 — — EP disclosed
CN-114302884-A Substituted pyridopyrimidinone based compounds useful as T cell activators 百时美施贵宝公司 2022-04-08 — — CN disclosed
WO-2021127554-A1 COMBINATIONS OF DGK INHIBITORS AND CHECKPOINT ANTAGONISTS BRISTOL-MYERS SQUIBB COMPANY (US) 2021-06-24 — — WO disclosed
WO-2021041588-A1 SUBSTITUTED PYRIDOPYRIMIDINONYL COMPOUNDS USEFUL AS T CELL ACTIVATORS BRISTOL-MYERS SQUIBB COMPANY (US) 2021-03-04 — — WO disclosed
US-20210061802-A1 SUBSTITUTED PYRIDOPYRIMIDINONYL COMPOUNDS USEFUL AS T CELL ACTIVATORS SYNGENE INTERNATIONAL LIMITED (IN) 2021-03-04 — — 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 (5 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-11584747-B2 Substituted pyridopyrimidinonyl compounds useful as T cell activators DGKZ, DGKA, DGKG PDE2A 1693/4885CES2 4254/4885CES1 3187/4885
US-20210061802-A1 SUBSTITUTED PYRIDOPYRIMIDINONYL COMPOUNDS USEFUL AS T CELL ACTIVATORS DGKZ, DGKA, DGKG PDE2A 1693/4885CES2 4254/4885CES1 3187/4885
US-20240400563-A1 SUBSTITUTED PYRIDOPYRIMIDINONYL COMPOUNDS USEFUL AS T CELL ACTIVATORS DGKZ, DGKA, DGKG PDE2A 1693/4885CES2 4254/4885CES1 3187/4885
US-20240108654-A1 COMBINATION OF A T CELL THERAPY AND A DGK INHIBITOR DGKG, DGKA, DGKI PDE2A 2589/4885CES2 2442/4885CES1 1019/4885
US-20230089255-A1 COMBINATIONS OF DGK INHIBITORS AND CHECKPOINT ANTAGONISTS DGKA, DGKG, DGKB PDE2A 1720/4885CES2 4243/4885CES1 1219/4885

“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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