SCHEMBL2435848

SCHEMBL2435848

CC(=O)OCCOCn1c(C(C)=O)nc2nc(N)[nH]c(=O)c21

nearest known ligand 0.43

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
PNP P00491 11/20 0.43
KMT2A Q03164 4/20 0.39
MEN1 O00255 3/20 0.39
HBB P68871 2/20 0.38
MAPK1 P28482 2/20 0.38
TSHR P16473 2/20 0.38
MAPT P10636 1/20 0.38
USP2 O75604 1/20 0.34
EDNRA P25101 1/20 0.34
HTR2A P28223 1/20 0.34
RECQL P46063 1/20 0.34
BLM P54132 1/20 0.34
HSD17B10 Q99714 1/20 0.34
ALDH1A1 P00352 2/20 0.33
HPRT1 P00492 1/20 0.32
GAA P10253 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
SCHEMBL8177048 0.84 MAPT (0.40) PNPKMT2AMEN1MAPK1MAPT
SCHEMBL2434143 0.82 PNP (0.57) PNPKMT2AMEN1HBBMAPK1
SCHEMBL7816005 0.72 TYMS (0.56) PNPKMT2AMEN1
SCHEMBL7806221 0.71 TYMS (0.59) PNPKMT2AMEN1MAPTHSD17B10
SCHEMBL8781905 0.71 PNP (0.55) PNPKMT2AMEN1HBBMAPK1
SCHEMBL9566544 0.71 PNP (0.71) PNPKMT2AMEN1HBBMAPK1
SCHEMBL7814355 0.68 MEN1 (0.76) PNPKMT2AMEN1HBBMAPK1
SCHEMBL7814363 0.68 HPRT1 (0.55) PNPKMT2AMEN1HBBMAPK1
SCHEMBL8165565 0.68 PNP (0.51) PNPKMT2AMEN1HBBTSHR
SCHEMBL7813638 0.68 TYMS (0.60) PNPKMT2AMEN1MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2011114336-A1 PROCESS FOR THE ISOLATION OF GANCICLOVIR INTERMEDIATE HETERO RESEARCH FOUNDATION (IN) 2011-09-22 WO disclosed
EP-0862570-B1 PROCESS FOR THE PREPARATION OF 9- (2-HYDROXYETHOXY)METHYL]GUANINE CLARIANT LSM ITALIA SPA (IT) 2001-03-21 EP disclosed
EP-0976751-A1 A process for the isomerisation of an N-7 isomer into an N-9 isomer useful in the synthesis of acyclic nucleosides LUPIN LABORATORIES LIMITED (IN) 2000-02-02 EP disclosed
EP-0976751-A1 A process for the isomerisation of an N-7 isomer into an N-9 isomer useful in the synthesis of acyclic nucleosides LUPIN LABORATORIES LIMITED (IN) 2000-02-02 EP disclosed
EP-0862570-A1 PROCESS FOR THE PREPARATION OF 9- (2-HYDROXYETHOXY)METHYL]GUANINE ARCHIMICA S.P.A. (IT) 1998-09-09 EP disclosed
EP-0806425-A1 An improved regiospecific process for synthesis of acyclic nucleosides LUPIN LABORATORIES LIMITED (IN) 1997-11-12 EP disclosed
WO-1997018211-A1 PROCESS FOR THE PREPARATION OF 9-[(2-HYDROXYETHOXY)METHYL]GUANINE ARCHIMICA S.P.A. (IT) 1997-05-22 WO disclosed