SCHEMBL13865274

SCHEMBL13865274

Cc1cnc(CNC(=O)OC(C)(C)C)nc1

nearest known ligand 0.48

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
L3MBTL1 Q9Y468 1/20 0.44
KDM4E B2RXH2 1/20 0.43
LMNA P02545 1/20 0.43
KDM4A O75164 1/20 0.42
NAMPT P43490 1/20 0.41
STK17B O94768 1/20 0.41
STK17A Q9UEE5 1/20 0.41
CACNA1H O95180 1/20 0.41
CACNA1B Q00975 1/20 0.41
CACNA1C Q13936 1/20 0.41
CYP1A2 P05177 1/20 0.40
MAPKAPK2 P49137 3/20 0.40
TDP1 Q9NUW8 1/20 0.39
ATR Q13535 1/20 0.39
GFER P55789 1/20 0.39
KCNA5 P22460 1/20 0.38
CYP3A4 P08684 1/20 0.38

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
SCHEMBL24756661 0.86 MAPKAPK2 (0.44) L3MBTL1KDM4ELMNAKDM4ANAMPT
SCHEMBL18591337 0.86 L3MBTL1 (0.43) L3MBTL1KDM4ELMNAKDM4ANAMPT
SCHEMBL15240003 0.86 STK17B (0.46) L3MBTL1KDM4ELMNAKDM4ANAMPT
SCHEMBL25097603 0.86 L3MBTL1 (0.43) L3MBTL1KDM4ELMNAKDM4ANAMPT
SCHEMBL21106557 0.86 L3MBTL1 (0.43) L3MBTL1KDM4ELMNAKDM4ANAMPT
SCHEMBL31565511 0.84 NAMPT (0.43) L3MBTL1KDM4ELMNAKDM4ANAMPT
SCHEMBL19762496 0.84 L3MBTL1 (0.44) L3MBTL1KDM4ELMNAKDM4ANAMPT
SCHEMBL23251840 0.84 L3MBTL1 (0.45) L3MBTL1KDM4ELMNAKDM4ANAMPT
SCHEMBL17035934 0.83 KDM4A (0.47) L3MBTL1KDM4ELMNAKDM4ANAMPT
SCHEMBL1191802 0.83 L3MBTL1 (0.41) L3MBTL1KDM4ELMNAKDM4ANAMPT

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 13 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2024137329-A1 METHODS FOR THE SYNTHESIS OF COMPLEMENT FACTOR D INHIBITORS AND INTERMEDIATES THEREOF ALEXION PHARMACEUTICALS, INC. (US) 2024-06-27 WO disclosed
WO-2023114198-A2 METHODS FOR THE SYNTHESIS OF COMPLEMENT FACTOR D INHIBITORS ALEXION PHARMACEUTICALS, INC. (US) 2023-06-22 WO disclosed
WO-2023114200-A2 METHODS FOR THE SYNTHESIS OF COMPLEMENT FACTOR D INHIBITORS AND INTERMEDIATES THEREOF ALEXION PHARMACEUTICALS, INC. (US) 2023-06-22 WO disclosed
US-20200290992-A1 Deuterium-Substituted Pyridin- And Pyrimidin-2-yl-Methylamine Compounds AUSPEX PHARMACEUTICALS, INC. 2020-09-17 US disclosed
US-20200290992-A1 Deuterium-Substituted Pyridin- And Pyrimidin-2-yl-Methylamine Compounds AUSPEX PHARMACEUTICALS, INC. 2020-09-17 US disclosed
US-10626105-B2 Deuterium-substituted pyridin- and pyrimidin-2-yl-methylamine compounds AUSPEX PHARMACEUTICALS, INC. (US) 2020-04-21 US disclosed
US-10626105-B2 Deuterium-substituted pyridin- and pyrimidin-2-yl-methylamine compounds AUSPEX PHARMACEUTICALS, INC. (US) 2020-04-21 US disclosed
WO-2018057576-A1 DEUTERIUM-SUBSTITUTED PYRIDIN- AND PYRIMIDIN-2-YL-METHYLAMINE COMPOUNDS AUSPEX PHARMACEUTICALS, INC. (US) 2018-03-29 WO disclosed
US-20180079742-A1 Deuterium-Substituted Pyridin- And Pyrimidin-2-yl-Methylamine Compounds AUSPEX PHARMACEUTICALS, INC. 2018-03-22 US disclosed
US-20180079742-A1 Deuterium-Substituted Pyridin- And Pyrimidin-2-yl-Methylamine Compounds AUSPEX PHARMACEUTICALS, INC. 2018-03-22 US disclosed
US-20180079742-A1 Deuterium-Substituted Pyridin- And Pyrimidin-2-yl-Methylamine Compounds AUSPEX PHARMACEUTICALS, INC. 2018-03-22 US disclosed
US-20090118507-A1 Method for Preparing (3-Chloro-4-Fluorophenyl)-(4-Fluoro-4--Piperidin-1-Yl)-Methanone and Novel Intermediate Pyrimidine Derivatives PIERRE FABRE MEDICAMENT (FR) 2009-05-07 US disclosed
US-20090118507-A1 Method for Preparing (3-Chloro-4-Fluorophenyl)-(4-Fluoro-4--Piperidin-1-Yl)-Methanone and Novel Intermediate Pyrimidine Derivatives PIERRE FABRE MEDICAMENT (FR) 2009-05-07 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 (4 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-20200290992-A1 Deuterium-Substituted Pyridin- And Pyrimidin-2-yl-Methylamine Compounds HTR2C, HTR5A, HTR1A L3MBTL1 4729/4885KDM4E 1260/4885LMNA 1738/4885
US-20180079742-A1 Deuterium-Substituted Pyridin- And Pyrimidin-2-yl-Methylamine Compounds HTR2C, HTR5A, HTR1A L3MBTL1 4729/4885KDM4E 1260/4885LMNA 1738/4885
US-10626105-B2 Deuterium-substituted pyridin- and pyrimidin-2-yl-methylamine compounds HTR2C, HTR5A, HTR1A L3MBTL1 4729/4885KDM4E 1260/4885LMNA 1738/4885
US-20090118507-A1 Method for Preparing (3-Chloro-4-Fluorophenyl)-(4-Fluoro-4--Piperidin-1-Yl)-Methanone and Novel Intermediate Pyrimidine Derivatives DNMT1, MCM4, MCM5 L3MBTL1 4819/4885KDM4E 684/4885LMNA 279/4885

“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.