SCHEMBL2370789

SCHEMBL2370789

CC1(C)C=C(B2OC(C)(C)C(C)(C)O2)CCO1

nearest known ligand 0.53

Predicted protein targets (top 4)

geneUniProtsupporting neighboursconfidence
▸ MAPK1 P28482 1/20 0.53
▸ P2RX7 Q99572 1/20 0.47
▸ LPL P06858 3/20 0.32
▸ LIPG Q9Y5X9 3/20 0.32

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
SCHEMBL19184946 0.76 MAPK1 (0.42) MAPK1P2RX7
SCHEMBL24514841 0.72 P2RX7 (0.50) MAPK1P2RX7LPLLIPG
SCHEMBL14330689 0.70 P2RX7 (0.57) MAPK1P2RX7LPLLIPG
SCHEMBL3655929 0.69 P2RX7 (0.47) MAPK1P2RX7LPLLIPG
SCHEMBL29082175 0.69 P2RX7 (0.56) MAPK1P2RX7LPLLIPG
SCHEMBL67926 0.69 MAPK1 (1.00) MAPK1P2RX7LPLLIPG
SCHEMBL30965858 0.69 P2RX7 (0.80) MAPK1P2RX7LPLLIPG
SCHEMBL31570452 0.68 P2RX7 (0.55) MAPK1P2RX7LPLLIPG
SCHEMBL20867989 0.68 MAPK1 (0.71) MAPK1P2RX7LPLLIPG
Dioxane SCHEMBL1995894 0.67 MAPK1 (0.93) MAPK1P2RX7LPLLIPG

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260138998-A1 GLP-1 RECEPTOR AGONISTS AND METHODS OF USE MERCK SHARP & DOHME LLC (US) 2026-05-21 — — US disclosed
US-12037339-B2 Substituted imidazoles as GLP-1 receptor agonists ECCOGENE INC. (US) 2024-07-16 — — US disclosed
US-12037339-B2 Substituted imidazoles as GLP-1 receptor agonists ECCOGENE INC. (US) 2024-07-16 — — US disclosed
EP-3959213-B1 PYRIMIDINE JAK INHIBITORS FOR THE TREATMENT OF SKIN DISEASES THERAVANCE BIOPHARMA R&D IP LLC (US) 2024-06-05 — — EP disclosed
CN-117069743-A GLP-1 receptor agonist 北京盛诺基医药科技股份有限公司 2023-11-17 — — CN disclosed
US-11584751-B1 Substituted imidazoles as GLP-1 receptor agonists ECCOGENE (SHANGHAI) CO., LTD. (CN) 2023-02-21 — — US disclosed
US-20230051320-A1 TETRAHYDROPYRAZOLO-PYRAZINYL-DIHYDROIMIDAZOLONE OR TETRAHYDROPYRAZOLO-PYRIDINYL-DIHYDROIMIDAZOLONE COMPOUNDS AND METHODS OF USING SAME ECCOGENE INC. 2023-02-16 — — US disclosed
US-11439641-B2 Pyrimidine JAK inhibitors for the treatment of skin diseases THERAVANCE BIOPHARMA R&D IP, LLC (US) 2022-09-13 — — US disclosed
EP-3959213-A1 PYRIMIDINE JAK INHIBITORS FOR THE TREATMENT OF SKIN DISEASES Theravance Biopharma R&D IP, LLC (US) 2022-03-02 — — EP disclosed
EP-3689875-B1 USE OF TRIAZOLOPYRIMIDINE, TRIAZOLOPYRIDINE COMPOUNDS AND COMPOSITION THEREOF FOR TREATING PRC2-MEDIATED DISEASES SHANGHAI INST MATERIA MEDICA CAS (CN) 2021-10-13 — — EP disclosed
US-20140213572-A1 UNSATURATED NITROGEN HETEROCYCLIC COMPOUNDS USEFUL AS PDE10 INHIBITORS AMGEN INC. (US) 2014-07-31 — — US disclosed
EP-2569300-A1 NITROGEN HETEROCYCLIC COMPOUNDS USEFUL AS PDE10 INHIBITORS Amgen Inc. (US) 2013-03-20 — — EP disclosed
EP-2547685-A1 SPIRO-TETRACYCLIC RING COMPOUNDS AS BETA - SECRETASE MODULATORS Amgen Inc. (US) 2013-01-23 — — EP disclosed
US-20110306587-A1 UNSATURATED NITROGEN HETEROCYCLIC COMPOUNDS USEFUL AS PDE10 INHIBITORS AMGEN INC. 2011-12-15 — — US disclosed
US-20110306587-A1 UNSATURATED NITROGEN HETEROCYCLIC COMPOUNDS USEFUL AS PDE10 INHIBITORS AMGEN INC. 2011-12-15 — — US disclosed
US-20110306587-A1 UNSATURATED NITROGEN HETEROCYCLIC COMPOUNDS USEFUL AS PDE10 INHIBITORS AMGEN INC. 2011-12-15 — — US disclosed
WO-2011143365-A1 NITROGEN HETEROCYCLIC COMPOUNDS USEFUL AS PDE10 INHIBITORS AMGEN INC. (US) 2011-11-17 — — WO disclosed
WO-2011143365-A1 NITROGEN HETEROCYCLIC COMPOUNDS USEFUL AS PDE10 INHIBITORS AMGEN INC. (US) 2011-11-17 — — WO disclosed
US-20110251190-A1 SPIRO-TETRACYCLIC RING COMPOUNDS AS BETA-SECRETASE MODULATORS AND METHODS OF USE AMGEN INC. (US) 2011-10-13 — — US disclosed
WO-2011115938-A1 SPIRO-TETRACYCLIC RING COMPOUNDS AS BETA - SECRETASE MODULATORS AMGEN INC. (US) 2011-09-22 — — WO 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 (8 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-11439641-B2 Pyrimidine JAK inhibitors for the treatment of skin diseases JAK1, JAK3, JAK2 MAPK1 281/4885P2RX7 120/4885LPL 4815/4885
US-20140213572-A1 UNSATURATED NITROGEN HETEROCYCLIC COMPOUNDS USEFUL AS PDE10 INHIBITORS PDE10A, PDE2A, PDE3A MAPK1 1417/4885P2RX7 3722/4885LPL 156/4885
US-11584751-B1 Substituted imidazoles as GLP-1 receptor agonists GLP1R, GIPR, SLC5A1 MAPK1 328/4885P2RX7 189/4885LPL 1514/4885
US-20230051320-A1 TETRAHYDROPYRAZOLO-PYRAZINYL-DIHYDROIMIDAZOLONE OR TETRAHYDROPYRAZOLO-PYRIDINYL-DIHYDROIMIDAZOLONE COMPOUNDS AND METHODS OF USING SAME GLP1R, SLC5A1, GIPR MAPK1 493/4885P2RX7 175/4885LPL 1472/4885
US-12037339-B2 Substituted imidazoles as GLP-1 receptor agonists GLP1R, GIPR, SLC5A1 MAPK1 328/4885P2RX7 189/4885LPL 1514/4885
US-20260138998-A1 GLP-1 RECEPTOR AGONISTS AND METHODS OF USE GLP1R, GIPR, GPR119 MAPK1 1154/4885P2RX7 202/4885LPL 895/4885
US-20110251190-A1 SPIRO-TETRACYCLIC RING COMPOUNDS AS BETA-SECRETASE MODULATORS AND METHODS OF USE BACE1, BACE2, APP MAPK1 3616/4885P2RX7 1520/4885LPL 1651/4885
US-20110306587-A1 UNSATURATED NITROGEN HETEROCYCLIC COMPOUNDS USEFUL AS PDE10 INHIBITORS PDE10A, PDE2A, PDE3A MAPK1 1417/4885P2RX7 3722/4885LPL 156/4885

“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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