SCHEMBL16181520

SCHEMBL16181520

CCCCOc1c(C(=O)OCC)n(CC=O)cc(C(=O)OCC)c1=O

nearest known ligand 0.41

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 3/20 0.41
LMNA P02545 2/20 0.41
ALDH1A1 P00352 3/20 0.39
KDM4E B2RXH2 3/20 0.39
CYP1A2 P05177 1/20 0.39
HTT P42858 1/20 0.39
CNR1 P21554 1/20 0.38
TDP1 Q9NUW8 2/20 0.38
NPC1 O15118 1/20 0.37
RAB9A P51151 1/20 0.37
HSD17B10 Q99714 1/20 0.37
TSHR P16473 2/20 0.36
L3MBTL1 Q9Y468 1/20 0.36
STAT3 P40763 1/20 0.35
POLB P06746 1/20 0.35
PKM P14618 1/20 0.34
BAZ2B Q9UIF8 1/20 0.34
BAZ2A Q9UIF9 1/20 0.34
MAPT P10636 2/20 0.34
MEN1 O00255 1/20 0.34

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
SCHEMBL2601037 0.87 PLA2G4A (0.38) KMT2ALMNAALDH1A1KDM4ECYP1A2
SCHEMBL17928514 0.83 TSHR (0.39) LMNAALDH1A1KDM4ECNR1RAB9A
SCHEMBL15143640 0.83 ALDH1A1 (0.38) KMT2ALMNAALDH1A1KDM4ECYP1A2
SCHEMBL18854210 0.82 TSHR (0.45) KMT2ALMNAALDH1A1KDM4ETDP1
SCHEMBL10239432 0.82 KMT2A (0.37) KMT2ALMNAALDH1A1KDM4ECYP1A2
SCHEMBL19276446 0.80 ALDH1A1 (0.37) KMT2ALMNAALDH1A1KDM4ECYP1A2
SCHEMBL16181523 0.79 KMT2A (0.45) KMT2ALMNAALDH1A1KDM4ECYP1A2
SCHEMBL16402299 0.78 TSHR (0.43) KMT2ALMNAALDH1A1KDM4ETDP1
SCHEMBL12264126 0.77 THRA (0.37) KMT2AALDH1A1KDM4EHTTTDP1
SCHEMBL2601040 0.77 ALDH1A1 (0.45) KMT2ALMNAALDH1A1CYP1A2CNR1

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
US-9802959-B2 Method of producing (4R,12aS)-7,9-dihalo-4-methyl-3,4,12,12a-tetrahydro-2H-pyrido[1′,2′:4,5]pyrazino[2,1-b][1,3]oxazine-6,8-diones SHIONOGI & CO., LTD. (JP) 2017-10-31 US disclosed
US-20170240564-A1 METHODS OF PRODUCING COMPOUNDS HAVING HIV INTEGRASE INHIBITORY ACTIVITY SHIONOGI & CO., LTD. (JP) 2017-08-24 US disclosed
US-9650394-B2 Methods of producing substituted (3S,11aR)-6-hydroxy-3-methyl-5,7-dioxo-2,3,5,7,11,11a-Hexahydrooxazolo[3,2-a]pyrido[1,2-d]pyrazine-8-carboxamides SHIONOGI & CO., LTD. (JP) 2017-05-16 US disclosed
US-9505783-B2 Method of producing pyrone and pyridone derivatives SHIONOGI & CO., LTD. (JP) 2016-11-29 US disclosed
EP-2602260-B1 PROCESS FOR PREPARING COMPOUND HAVING HIV INTEGRASE INHIBITORY ACTIVITY SHIONOGI & CO (JP) 2016-09-28 EP disclosed
US-20160229870-A1 METHODS OF PRODUCING COMPOUNDS HAVING HIV INTEGRASE INHIBITORY ACTIVITY SHIONOGI & CO., LTD. (JP) 2016-08-11 US disclosed
EP-2412709-B1 PROCESS FOR PRODUCING PYRONE AND PYRIDONE DERIVATIVES SHIONOGI & CO (JP) 2016-05-18 EP disclosed
US-9321789-B2 Methods of producing substituted (4R,12AS)-7-hydroxy-4-methyl-6,8-dioxo-3,4,6,8,12,12A-hexahydro-2H-pyrido[1′,2′:4,5]pyrazino[2,1-B][1,3]oxazine-9-carboxamides SHINOGI & CO., LTD. (JP) 2016-04-26 US disclosed
US-20160002211-A1 METHOD OF PRODUCING PYRONE AND PYRIDONE DERIVATIVES SHIONOGI & CO., LTD. (JP) 2016-01-07 US disclosed
US-20150038702-A1 Method of producing compounds having HIV integrase inhivitory activity SHINOGI & CO., LTD. (JP) 2015-02-05 US disclosed
US-20150031876-A1 METHOD FOR PRODUCING PYRONE AND PYRIDONE DERIVATIVES SHIONOGI & CO., LTD. (JP) 2015-01-29 US disclosed
US-8865907-B2 Method of producing pyrone and pyridone derivatives SHIONOGI & CO., LTD. (JP) 2014-10-21 US disclosed
US-20140011995-A1 Process for Preparing Compound Having HIV Integrase Inhibitory Activity SHINOGI & CO., LTD (JP) 2014-01-09 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 (6 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-20150038702-A1 Method of producing compounds having HIV integrase inhivitory activity XDH, IMPDH1, IMPA1 KMT2A 1655/4885LMNA 1129/4885ALDH1A1 2362/4885
US-20150031876-A1 METHOD FOR PRODUCING PYRONE AND PYRIDONE DERIVATIVES PNPO, PDXK, CYP3A5 KMT2A 3600/4885LMNA 472/4885ALDH1A1 2038/4885
US-20170240564-A1 METHODS OF PRODUCING COMPOUNDS HAVING HIV INTEGRASE INHIBITORY ACTIVITY XDH, DRD4, PYM1 KMT2A 1061/4885LMNA 2283/4885ALDH1A1 2776/4885
US-20160229870-A1 METHODS OF PRODUCING COMPOUNDS HAVING HIV INTEGRASE INHIBITORY ACTIVITY XDH, VRK2, PYM1 KMT2A 1422/4885LMNA 1681/4885ALDH1A1 2538/4885
US-20140011995-A1 Process for Preparing Compound Having HIV Integrase Inhibitory Activity DRD4, XDH, CCND2 KMT2A 1048/4885LMNA 2143/4885ALDH1A1 3180/4885
US-20160002211-A1 METHOD OF PRODUCING PYRONE AND PYRIDONE DERIVATIVES PNPO, PDXK, CYP3A5 KMT2A 3654/4885LMNA 472/4885ALDH1A1 2121/4885

“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.