SCHEMBL720108

SCHEMBL720108

CC(NP(=O)(Cl)Oc1cccc2ncccc12)C(=O)O

nearest known ligand 0.42

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 2/20 0.40
KMT2A Q03164 2/20 0.40
NR3C1 P04150 2/20 0.40
KDM4E B2RXH2 2/20 0.40
MAPT P10636 2/20 0.40
L3MBTL1 Q9Y468 2/20 0.39
SMN1; SMN2 Q16637 2/20 0.39
HSD17B10 Q99714 1/20 0.39
NSD2 O96028 1/20 0.39
FABP5 Q01469 1/20 0.39
ALDH1A1 P00352 3/20 0.39
PABPC1 P11940 2/20 0.39
EIF4H Q15056 2/20 0.39
SCN9A Q15858 1/20 0.39
POLB P06746 1/20 0.39
LMNA P02545 1/20 0.38
HTT P42858 1/20 0.38
RECQL P46063 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
SCHEMBL722154 0.89 NR3C1 (0.41) MEN1KMT2ANR3C1KDM4EMAPT
SCHEMBL10208208 0.85 NR3C1 (0.39) MEN1KMT2ANR3C1L3MBTL1SMN1; SMN2
SCHEMBL1273621 0.82 ALDH1A1 (0.43) MEN1KMT2AKDM4ESMN1; SMN2HSD17B10
SCHEMBL719597 0.82 ALDH1A1 (0.43) MEN1KMT2AKDM4ESMN1; SMN2HSD17B10
SCHEMBL723660 0.81 CASP1 (0.37) NR3C1L3MBTL1SMN1; SMN2HSD17B10ALDH1A1
SCHEMBL723661 0.81 CASP1 (0.37) NR3C1L3MBTL1SMN1; SMN2HSD17B10ALDH1A1
SCHEMBL1744377 0.79 NR3C1 (0.39) MEN1KMT2ANR3C1L3MBTL1SMN1; SMN2
SCHEMBL723763 0.79 SCN9A (0.39) NR3C1L3MBTL1SMN1; SMN2HSD17B10ALDH1A1
SCHEMBL723762 0.79 SCN9A (0.39) NR3C1L3MBTL1SMN1; SMN2HSD17B10ALDH1A1
SCHEMBL724167 0.76 ALDH1A1 (0.50) MEN1KMT2AMAPTALDH1A1PABPC1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8759318-B2 Phosphoramidate derivatives of guanosine nucleoside compounds for treatment of viral infections INHIBITEX, INC. (US) 2014-06-24 US disclosed
US-20120052046-A1 Phosphoramidate Derivatives of Guanosine Nucleoside Compunds for Treatment of Viral Infections UNIVERSITY COLLEGE CARDIFF CONSULTANTS LIMITED (GB) 2012-03-01 US disclosed
EP-2385951-A2 PHOSPHORAMIDATE DERIVATIVES OF GUANOSINE NUCLEOSIDE COMPOUNDS FOR TREATMENT OF VIRAL INFECTIONS University College Cardiff Consultants, Ltd. (GB) 2011-11-16 EP disclosed
US-20110254856-A1 MOBILE TERMINAL AND METHOD OF CONTROLLING OPERATION OF THE MOBILE TERMINAL LG ELECTRONICS INC. (KR) 2011-10-20 US disclosed
WO-2010081082-A2 PHOSPHORAMIDATE DERIVATIVES OF GUANOSINE NUCLEOSIDE COMPOUNDS FOR TREATMENT OF VIRAL INFECTIONS UNIVERSITY COLLEGE OF CARDIFF CONSULTANTS LIMITED (GB) 2010-07-15 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 (1 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-20120052046-A1 Phosphoramidate Derivatives of Guanosine Nucleoside Compunds for Treatment of Viral Infections PNP, SAMHD1, MTAP MEN1 1740/4885KMT2A 3637/4885NR3C1 2166/4885

“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.