SCHEMBL722413

SCHEMBL722413

O=C(O)C(NP(=O)(Cl)Oc1cccc2ccccc12)c1ccccc1

nearest known ligand 0.41

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 6/20 0.40
KDM4E B2RXH2 3/20 0.40
KMT2A Q03164 3/20 0.40
HPGD P15428 2/20 0.40
TDP1 Q9NUW8 1/20 0.40
OGG1 O15527 1/20 0.40
HSD17B10 Q99714 2/20 0.40
PGR P06401 1/20 0.40
GAA P10253 1/20 0.40
PTGS1 P23219 1/20 0.40
MAPK1 P28482 1/20 0.40
TACR3 P29371 1/20 0.39
ELANE P08246 2/20 0.38
MEN1 O00255 2/20 0.38
LMNA P02545 2/20 0.38
SMN1; SMN2 Q16637 1/20 0.38
SLC6A2 P23975 1/20 0.37
SLC6A4 P31645 1/20 0.37
HTT P42858 1/20 0.37
MITF O75030 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
SCHEMBL722519 0.89 TACR3 (0.46) ALDH1A1KDM4EKMT2AHSD17B10TACR3
SCHEMBL10208298 0.85 ALDH1A1 (0.41) ALDH1A1KDM4EKMT2AHPGDTDP1
SCHEMBL10208309 0.85 ALDH1A1 (0.41) ALDH1A1KDM4EKMT2AHPGDTDP1
SCHEMBL1743892 0.84 KMT2A (0.44) ALDH1A1KDM4EKMT2AHPGDTDP1
SCHEMBL10208315 0.84 KMT2A (0.42) ALDH1A1KDM4EKMT2AHPGDTDP1
SCHEMBL10208307 0.84 KMT2A (0.42) ALDH1A1KDM4EKMT2AHPGDTDP1
SCHEMBL10208314 0.84 KMT2A (0.44) ALDH1A1KDM4EKMT2AHPGDTDP1
SCHEMBL719597 0.83 ALDH1A1 (0.43) ALDH1A1KDM4EKMT2AHPGDTDP1
SCHEMBL1273621 0.83 ALDH1A1 (0.43) ALDH1A1KDM4EKMT2AHPGDTDP1
SCHEMBL721002 0.82 MEN1 (0.42) ALDH1A1KDM4EKMT2AHPGDHSD17B10

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 ALDH1A1 4139/4885KDM4E 4140/4885KMT2A 3637/4885

“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.