SCHEMBL1273472

SCHEMBL1273472

CC(C)(C)OC(=O)N1[C@@H]2C[C@@H]2C[C@@H]1C=O

nearest known ligand 0.45

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
CHRM2 P08172 1/20 0.45
CHRM1 P11229 1/20 0.45
CHRM3 P20309 1/20 0.45
NR1H2 P55055 1/20 0.42
DPP4 P27487 4/20 0.39
PREP P48147 4/20 0.39
HSD11B1 P28845 1/20 0.33
CTSK P43235 1/20 0.33
USP2 O75604 1/20 0.33
SMN1; SMN2 Q16637 1/20 0.33
ABCB1 P08183 1/20 0.32
EPHX2 P34913 1/20 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
SCHEMBL26816592 1.00 CHRM2 (0.45) CHRM2CHRM1CHRM3NR1H2DPP4
SCHEMBL26782680 1.00 CHRM2 (0.45) CHRM2CHRM1CHRM3NR1H2DPP4
SCHEMBL18023493 1.00 CHRM2 (0.45) CHRM2CHRM1CHRM3NR1H2DPP4
SCHEMBL16006532 1.00 CHRM2 (0.45) CHRM2CHRM1CHRM3NR1H2DPP4
SCHEMBL29102312 1.00 CHRM2 (0.45) CHRM2CHRM1CHRM3NR1H2DPP4
SCHEMBL1572414 1.00 CHRM2 (0.45) CHRM2CHRM1CHRM3NR1H2DPP4
SCHEMBL19664035 1.00 CHRM2 (0.45) CHRM2CHRM1CHRM3NR1H2DPP4
SCHEMBL1293236 1.00 CHRM2 (0.45) CHRM2CHRM1CHRM3NR1H2DPP4
SCHEMBL29102387 1.00 CHRM2 (0.45) CHRM2CHRM1CHRM3NR1H2DPP4
SCHEMBL1293235 1.00 CHRM2 (0.45) CHRM2CHRM1CHRM3NR1H2DPP4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260137674-A1 COMBINATION THERAPY USING A KRAS G12D INHIBITOR, AND A NUCLEOSIDE ANALOG, AND/OR A MICROTUBULE INHIBITOR INCYTE CORP (US) 2026-05-21 US disclosed
WO-2026090323-A1 COMBINATION THERAPY USING A KRAS G12D INHIBITOR, AND A NUCLEOSIDE ANALOG, AND/OR A MICROTUBULE INHIBITOR AND ITS USE IN THE TREATMENT OF CANCER INCYTE CORPORATION (US) 2026-04-30 WO disclosed
WO-2026090333-A1 COMBINATION USING A KRAS G12D INHIBITOR AND CHEMOTHERAPY COMBINATIONS AS WELL AS THEIR USE IN THE TREATMENT OF CANCER INCYTE CORPORATION (US) 2026-04-30 WO disclosed
US-20250368641-A1 QUINOLINE COMPOUNDS AS INHIBITORS OF KRAS INCYTE CORP (US) 2025-12-04 US disclosed
US-20250304601-A1 Processes for Preparing KRAS Inhibitors INCYTE CORPORATION 2025-10-02 US disclosed
US-12378243-B2 Quinoline compounds as inhibitors of KRAS INCYTE CORPORATION (US) 2025-08-05 US disclosed
WO-2025080589-A1 PROCESSES FOR PREPARING KRAS INHIBITORS INCYTE CORPORATION (US) 2025-04-17 WO disclosed
WO-2025080593-A1 COMBINATION THERAPY USING A KRAS G12D INHIBITOR AND PD-1 INHIBITOR OR PD-L1 INHIBITOR INCYTE CORPORATION (US) 2025-04-17 WO disclosed
WO-2025080592-A1 COMBINATION COMPRISING A KRAS G12D INHIBITOR AND AN EGFR INHIBITOR FOR USE IN THE TREATMENT OF CANCER INCYTE CORPORATION (US) 2025-04-17 WO disclosed
WO-2025080585-A1 CRYSTALLINE FORMS OF 3-(1-(( 1 R,4R,5S)-2-AZABICYCLO[2.1.1 ]HEXAN-5-YL)-2-(( 1 R,3R,5R)-2-( CYCLOPROPANECARBONYL)-2-AZABICYCLO[3.1.0]HEXAN-3-YL)-7-(2,3-DICHLOROPHENYL)-6-FLUORO-4-METHYL-1 H-PYRROLO[3,2-C]QUINOLIN-8-YL)PROPANENITRILE INCYTE CORPORATION (US) 2025-04-17 WO disclosed
WO-2023064857-A1 QUINOLINE COMPOUNDS AS INHIBITORS OF KRAS INCYTE CORPORATION (US) 2023-04-20 WO disclosed
WO-2022066734-A1 PYRROLO[3,2-C]PYRIDIN-4-ONE DERIVATIVES USEFUL IN THE TREATMENT OF CANCER SCORPION THERAPEUTICS, INC. (US) 2022-03-31 WO disclosed
US-20110034469-A1 Heterocyclic Compound TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2011-02-10 US disclosed
US-20090111825-A1 THIOPHENE 1,2,4-TRIAZOLE DERIVATIVES AS MODULATORS OF MGLUR5 ASTRAZENECA AB (SE) 2009-04-30 US disclosed
US-20090111825-A1 THIOPHENE 1,2,4-TRIAZOLE DERIVATIVES AS MODULATORS OF MGLUR5 ASTRAZENECA AB (SE) 2009-04-30 US disclosed
US-20090111825-A1 THIOPHENE 1,2,4-TRIAZOLE DERIVATIVES AS MODULATORS OF MGLUR5 ASTRAZENECA AB (SE) 2009-04-30 US disclosed
WO-2009054791-A1 FUSED PYRROLIDINE 1,2,4-TRIAZOLE DERIVATIVES AS MODULATORS OF MGLUR5 ASTRAZENECA AB (SE) 2009-04-30 WO disclosed
US-20090111820-A1 FUSED PYRROLIDINE 1,2,4-TRIAZOLE DERIVATIVES AS MODULATORS OF MGLUR5 ASTRAZENECA AB (SE) 2009-04-30 US disclosed
US-20090111820-A1 FUSED PYRROLIDINE 1,2,4-TRIAZOLE DERIVATIVES AS MODULATORS OF MGLUR5 ASTRAZENECA AB (SE) 2009-04-30 US disclosed
WO-2009054793-A1 THIOPHENE 1,2,4-TRIAZOLE DERIVATIVES AS MODULATORS OF MGLUR5 ASTRAZENECA AB (SE) 2009-04-30 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 (7 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-20110034469-A1 Heterocyclic Compound BIRC5, XIAP, BIRC2 CHRM2 3661/4885CHRM1 3517/4885CHRM3 3507/4885
US-20090111820-A1 FUSED PYRROLIDINE 1,2,4-TRIAZOLE DERIVATIVES AS MODULATORS OF MGLUR5 GRM5, GRIK5, GRM1 CHRM2 1852/4885CHRM1 1404/4885CHRM3 1107/4885
US-20250304601-A1 Processes for Preparing KRAS Inhibitors KRAS, NRAS, HRAS CHRM2 4871/4885CHRM1 4859/4885CHRM3 4861/4885
US-20090111825-A1 THIOPHENE 1,2,4-TRIAZOLE DERIVATIVES AS MODULATORS OF MGLUR5 GRM5, GRIK5, GRM1 CHRM2 1222/4885CHRM1 1043/4885CHRM3 737/4885
US-12378243-B2 Quinoline compounds as inhibitors of KRAS KRAS, NRAS, HRAS CHRM2 4782/4885CHRM1 4747/4885CHRM3 4777/4885
US-20260137674-A1 COMBINATION THERAPY USING A KRAS G12D INHIBITOR, AND A NUCLEOSIDE ANALOG, AND/OR A MICROTUBULE INHIBITOR KRAS, NRAS, DCTD CHRM2 4587/4885CHRM1 4603/4885CHRM3 4786/4885
US-20250368641-A1 QUINOLINE COMPOUNDS AS INHIBITORS OF KRAS KRAS, NRAS, HRAS CHRM2 4782/4885CHRM1 4747/4885CHRM3 4777/4885

“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.