SCHEMBL20560749

SCHEMBL20560749

Cc1ccnc(C(C)C)c1NC(=O)NC(=O)c1cc(F)c(Cl)nc1Cl

nearest known ligand 0.39

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
GAA P10253 1/20 0.39
KEAP1 Q14145 1/20 0.39
NFE2L2 Q16236 1/20 0.39
PKM P14618 2/20 0.37
MAPK1 P28482 1/20 0.37
RAB9A P51151 5/20 0.36
LMNA P02545 1/20 0.36
PYGL P06737 4/20 0.36
DHODH Q02127 5/20 0.35
NPC1 O15118 4/20 0.34
SMN1; SMN2 Q16637 2/20 0.33
CTNNB1 P35222 1/20 0.33
TCF7L2 Q9NQB0 1/20 0.33
TP53 P04637 1/20 0.33
CYP1A2 P05177 1/20 0.33
CYP2C19 P33261 1/20 0.33
MEN1 O00255 1/20 0.33
KMT2A Q03164 1/20 0.33

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
SCHEMBL29742271 1.00 GAA (0.39) GAAKEAP1NFE2L2PKMMAPK1
SCHEMBL29742278 1.00 GAA (0.39) GAAKEAP1NFE2L2PKMMAPK1
SCHEMBL28559681 0.92 DHODH (0.40) GAAKEAP1NFE2L2PKMMAPK1
SCHEMBL28562623 0.91 GAA (0.39) GAAKEAP1NFE2L2PKMMAPK1
SCHEMBL24455254 0.90 DHODH (0.37) GAAKEAP1NFE2L2PKMMAPK1
SCHEMBL28574410 0.90 DHODH (0.38) GAAKEAP1NFE2L2PKMMAPK1
SCHEMBL28576661 0.90 DHODH (0.38) GAAKEAP1NFE2L2PKMMAPK1
SCHEMBL28563781 0.90 DHODH (0.38) GAAKEAP1NFE2L2PKMMAPK1
SCHEMBL25665425 0.90 KEAP1 (0.39) GAAKEAP1NFE2L2PKMMAPK1
SCHEMBL20560768 0.89 PKM (0.37) GAAPKMMAPK1RAB9ALMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4247813-B1 PROCESS FOR PREPARING 7-CHLORO-6-FLUORO-1-(2-ISOPROPYL-4-METHYLPYRIDIN-3- YL)PYRIDOF[2,3-D]PYRIMIDINE-2,4(1H,3H)-DIONE AMGEN INC (US) 2025-12-24 EP claimed
US-12441729-B2 Process for preparing 7-chloro-6-fluoro-1-(2-isopropyl-4-methylpyridin-3-yl)pyrido[2,3-d]pyrimidine-2,4(1H,3H)-dione AMGEN INC. (US) 2025-10-14 US claimed
US-20250129072-A1 PROCESS FOR PREPARING 7-CHLORO-6-FLUORO-1-(2-ISOPROPYL-4-METHYLPYRIDIN-3-YL)PYRIDO[2,3-D]PYRIMIDINE-2,4(1H,3H)-DIONE AMGEN INC. (US) 2025-04-24 US claimed
US-20240025896-A1 PROCESS FOR PREPARING 7-CHLORO-6-FLUORO-1-(2-ISOPROPYL-4-METHYLPYRIDIN-3-YL)PYRIDO[2,3-D]PYRIMIDINE-2,4(1H,3H)-DIONE AMGEN INC. (US) 2024-01-25 US claimed
CN-116507624-A Process for preparing 7-chloro-6-fluoro-1- (2-isopropyl-4-methylpyridin-3-yl) pyrido F [2,3-D ] pyrimidine-2, 4 (1H, 3H) -dione 美国安进公司 2023-07-28 CN claimed
CN-114907259-A Synthetic method of Sotolira intermediate 常州中氪生命科学技术有限公司 2022-08-16 CN claimed
EP-3974429-A1 PRECURSORS OF KRAS G12C INHIBITORS Amgen Inc. (US) 2022-03-30 EP claimed
EP-4700026-A3 PROCESS FOR PREPARING 7-CHLORO-6-FLUORO-1-(2-ISOPROPYL-4-METHYLPYRIDIN-3- YL)PYRIDOF[2,3-D]PYRIMIDINE-2,4(1H,3H)-DIONE Amgen Inc. (US) 2026-05-20 EP disclosed
US-12630547-B2 RAS protein degraders, pharmaceutical compositions thereof, and their therapeutic applications BIOTHERYX, INC. (US) 2026-05-19 US disclosed
EP-4234546-B1 IMPROVED SYNTHESIS OF KEY INTERMEDIATE OF KRAS G12C INHIBITOR COMPOUND AMGEN INC (US) 2026-04-15 EP disclosed
US-12582657-B2 Combination therapy including a KRAS G12C inhibitor and one or more additional pharmaceutically active agents for the treatment of cancers AMGEN INC. (US) 2026-03-24 US disclosed
EP-4685160-A2 COMBINATION THERAPY INCLUDING A KRASG12C INHIBITOR AND ONE OR MORE ADDITIONAL PHARMACEUTICALLY ACTIVE AGENTS FOR THE TREATMENT OF CANCERS Amgen Inc. (US) 2026-01-28 EP disclosed
US-20250388579-A1 SYNTHESIS OF KRAS G12C INHIBITOR COMPOUND AMGEN INC. (US) 2025-12-25 US disclosed
US-10519146-B2 KRAS G12C inhibitors and methods of using the same AMGEN INC. (US) 2019-12-31 US disclosed
US-20190077801-A1 INHIBITORS OF KRAS G12C AND METHODS OF USING THE SAME AMGEN INC. 2019-03-14 US disclosed
WO-2019051291-A1 INHIBITORS OF KRAS G12C AND METHODS OF USING THE SAME AMGEN INC. (US) 2019-03-14 WO disclosed
WO-2019051291-A1 INHIBITORS OF KRAS G12C AND METHODS OF USING THE SAME AMGEN INC. (US) 2019-03-14 WO disclosed
US-20190077801-A1 INHIBITORS OF KRAS G12C AND METHODS OF USING THE SAME AMGEN INC. 2019-03-14 US disclosed
WO-2018217651-A1 KRAS G12C INHIBITORS AND METHODS OF USING THE SAME AMGEN INC. (US) 2018-11-29 WO disclosed
US-20180334454-A1 KRAS G12C INHIBITORS AND METHODS OF USING THE SAME AMGEN INC. 2018-11-22 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 (9 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-12630547-B2 RAS protein degraders, pharmaceutical compositions thereof, and their therapeutic applications KRAS, RSU1, NRAS GAA 1458/4885KEAP1 726/4885NFE2L2 2351/4885
US-20240025896-A1 PROCESS FOR PREPARING 7-CHLORO-6-FLUORO-1-(2-ISOPROPYL-4-METHYLPYRIDIN-3-YL)PYRIDO[2,3-D]PYRIMIDINE-2,4(1H,3H)-DIONE HINT1, DPYD, NME2 GAA 1829/4885KEAP1 3753/4885NFE2L2 2327/4885
US-12441729-B2 Process for preparing 7-chloro-6-fluoro-1-(2-isopropyl-4-methylpyridin-3-yl)pyrido[2,3-d]pyrimidine-2,4(1H,3H)-dione HINT1, NME2, DPYD GAA 1800/4885KEAP1 3196/4885NFE2L2 2008/4885
US-20250129072-A1 PROCESS FOR PREPARING 7-CHLORO-6-FLUORO-1-(2-ISOPROPYL-4-METHYLPYRIDIN-3-YL)PYRIDO[2,3-D]PYRIMIDINE-2,4(1H,3H)-DIONE HINT1, NME2, DPYD GAA 1800/4885KEAP1 3196/4885NFE2L2 2008/4885
US-10519146-B2 KRAS G12C inhibitors and methods of using the same KRAS, NRAS, HRAS GAA 2321/4885KEAP1 344/4885NFE2L2 3211/4885
US-20190077801-A1 INHIBITORS OF KRAS G12C AND METHODS OF USING THE SAME KRAS, NRAS, HRAS GAA 2041/4885KEAP1 271/4885NFE2L2 2542/4885
US-20180334454-A1 KRAS G12C INHIBITORS AND METHODS OF USING THE SAME KRAS, NRAS, HRAS GAA 2321/4885KEAP1 344/4885NFE2L2 3211/4885
US-20250388579-A1 SYNTHESIS OF KRAS G12C INHIBITOR COMPOUND KRAS, NRAS, BRAF GAA 4799/4885KEAP1 1498/4885NFE2L2 1868/4885
US-12582657-B2 Combination therapy including a KRAS G12C inhibitor and one or more additional pharmaceutically active agents for the treatment of cancers KRAS, NRAS, BRAF GAA 4829/4885KEAP1 1062/4885NFE2L2 2617/4885

“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.