SCHEMBL14969331

SCHEMBL14969331

CC(C)n1cc(C(=O)O)c(=O)n(-c2ccccc2)c1=O

nearest known ligand 0.44

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 3/20 0.44
NOTUM Q6P988 3/20 0.43
ALDH1A1 P00352 2/20 0.43
MET P08581 1/20 0.42
KDM4E B2RXH2 2/20 0.42
GAA P10253 1/20 0.40
GSK3A P49840 2/20 0.40
GSK3B P49841 2/20 0.40
MAPT P10636 1/20 0.39
TYRO3 Q06418 3/20 0.39
PGR P06401 1/20 0.39
MERTK Q12866 2/20 0.38
PDE4A P27815 1/20 0.37
PDE4B Q07343 1/20 0.37
PDE4C Q08493 1/20 0.37
PDE4D Q08499 1/20 0.37

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
SCHEMBL19398124 0.90 KDM4E (0.45) KMT2AMETKDM4EGSK3AGSK3B
SCHEMBL29625543 0.88 KMT2A (0.48) KMT2AMETKDM4EGSK3AGSK3B
SCHEMBL19567654 0.88 NOTUM (0.47) KMT2ANOTUMALDH1A1METKDM4E
SCHEMBL14967303 0.87 NOTUM (0.47) NOTUMMETMERTK
SCHEMBL21785475 0.87 NOTUM (0.47) KMT2ANOTUMALDH1A1METKDM4E
SCHEMBL23071267 0.87 AXL (0.41) KMT2AMETMERTK
Hydrochloric Acid SCHEMBL31614377 0.87 KMT2A (0.47) KMT2AMETKDM4EGSK3AGSK3B
SCHEMBL19377769 0.85 ALKBH5 (0.43) KMT2ANOTUMALDH1A1METGSK3A
SCHEMBL23071280 0.85 NOTUM (0.52) NOTUMALDH1A1METTYRO3MERTK
SCHEMBL23071007 0.85 MET (0.44) METKDM4EGSK3AGSK3BMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2780338-B1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS IGNYTA INC (US) 2016-11-09 EP claimed
US-20140275077-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS CEPHALON, INC. (US) 2014-09-18 US claimed
US-20260042765-A1 PYRROLOTRIAZINE COMPOUNDS AS TAM INHIBITORS INCYTE CORP (US) 2026-02-12 US disclosed
US-12415809-B2 Pyrrolotriazine compounds as tam inhibitors INCYTE CORPORATION (US) 2025-09-16 US disclosed
US-20250188086-A1 SALTS OF TAM INHIBITORS INCYTE CORPORATION 2025-06-12 US disclosed
US-12187730-B2 Salts of TAM inhibitors INCYTE CORPORATION (US) 2025-01-07 US disclosed
CN-118930549-A Salts of pyrrolotriazine derivatives useful as TAM inhibitors 因赛特公司 2024-11-12 CN disclosed
CN-114456175-B Pyrrolotriazine compounds as TAM inhibitors 因赛特公司 2024-09-03 CN disclosed
CN-114456176-B Pyrrolotriazine compounds as TAM inhibitors 因赛特公司 2024-08-30 CN disclosed
US-12037323-B2 Uracil derivatives as Mer-AXL inhibitors BRISTOL-MYERS SQUIBB COMPANY (US) 2024-07-16 US disclosed
CN-111386273-B Salts of pyrrolotriazine derivatives useful as TAM inhibitors 因赛特公司 2024-06-14 CN disclosed
EP-2780338-B1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS IGNYTA INC (US) 2016-11-09 EP disclosed
EP-3045453-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS CEPHALON, INC. (US) 2016-07-20 EP disclosed
US-9120778-B2 Uracil derivatives as AXL and c-MET kinase inhibitors IGNYTA, INC. (US) 2015-09-01 US disclosed
US-20150210670-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS CEPHALON, INC. 2015-07-30 US disclosed
US-20150209358-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS CEPHALON, INC. 2015-07-30 US disclosed
US-9029538-B2 Uracil derivatives as AXL and c-MET kinase inhibitors IGNYTA, INC. (US) 2015-05-12 US disclosed
EP-2780338-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS Cephalon, Inc. (US) 2014-09-24 EP disclosed
US-20140275077-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS CEPHALON, INC. (US) 2014-09-18 US disclosed
WO-2013074633-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS CEPHALON, INC. (US) 2013-05-23 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-20260042765-A1 PYRROLOTRIAZINE COMPOUNDS AS TAM INHIBITORS MAP2K2, TTK, MAP2K5 KMT2A 806/4885NOTUM 1928/4885ALDH1A1 2069/4885
US-12037323-B2 Uracil derivatives as Mer-AXL inhibitors MERTK, DAPK1, AXL KMT2A 3563/4885NOTUM 4844/4885ALDH1A1 1072/4885
US-20250188086-A1 SALTS OF TAM INHIBITORS PI4KA, PI4KB, PIK3CA KMT2A 578/4885NOTUM 3709/4885ALDH1A1 3276/4885
US-12187730-B2 Salts of TAM inhibitors PI4KA, PI4KB, PIK3CA KMT2A 578/4885NOTUM 3709/4885ALDH1A1 3276/4885
US-20150210670-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS AXL, RET, BRAF KMT2A 822/4885NOTUM 4849/4885ALDH1A1 1561/4885
US-12415809-B2 Pyrrolotriazine compounds as tam inhibitors MERTK, MAP3K15, MAP3K5 KMT2A 640/4885NOTUM 4398/4885ALDH1A1 2279/4885
US-20140275077-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS AXL, RET, BRAF KMT2A 822/4885NOTUM 4849/4885ALDH1A1 1561/4885
US-20150209358-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS AXL, RET, BRAF KMT2A 822/4885NOTUM 4849/4885ALDH1A1 1561/4885

“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.