SCHEMBL6356953

SCHEMBL6356953

CCCc1nn(C)c(C(N)=O)c1NC(=O)c1cc([N+](=O)[O-])cnc1OCC

nearest known ligand 0.57

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
TERT O14746 5/20 0.57
SMN1; SMN2 Q16637 2/20 0.47
MAPT P10636 4/20 0.39
POLB P06746 1/20 0.39
KMT2A Q03164 3/20 0.36
MEN1 O00255 2/20 0.36
PDE5A O76074 2/20 0.36
PKM P14618 1/20 0.35
RECQL P46063 1/20 0.34
RAB9A P51151 4/20 0.34
NPC1 O15118 2/20 0.34
ALDH1A1 P00352 2/20 0.34
LMNA P02545 1/20 0.34
HPGD P15428 1/20 0.33

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
SCHEMBL6776964 0.84 PDE5A (0.44) TERTSMN1; SMN2MAPTPOLBKMT2A
SCHEMBL6450443 0.80 PDE5A (0.49) TERTSMN1; SMN2MAPTPOLBKMT2A
SCHEMBL6895181 0.79 TERT (0.60) TERTSMN1; SMN2MAPTPOLBPDE5A
SCHEMBL6443282 0.77 PDE5A (0.63) TERTKMT2APDE5AALDH1A1
SCHEMBL1792 0.75 TERT (0.65) TERTMAPTKMT2AMEN1RAB9A
SCHEMBL3579254 0.75 PDE5A (0.46) TERTMAPTPOLBKMT2AMEN1
SCHEMBL6772078 0.74 MAPT (0.46) SMN1; SMN2MAPTPOLBKMT2APKM
SCHEMBL6447286 0.73 MEN1 (0.39) POLBKMT2AMEN1PDE5APKM
SCHEMBL7960724 0.73 TERT (0.65) TERTSMN1; SMN2MAPTPDE5ARAB9A
SCHEMBL8125815 0.73 TERT (0.62) TERTSMN1; SMN2MAPTKMT2APDE5A

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-20050143367-A1 Process for the preparation of pyrazolo[4,3-d]pyrimidin-7-one compounds and intermediates thereof PFIZER INC 2005-06-30 US disclosed
US-6809200-B2 REACTING 5-ACETYL-N-(3-(AMINOCARBONYL)-5-ETHYL-1-(1-ETHYL-3-AZETIDINYL)-1H-PYRAZOL4 -YL)-2-ETHOXYNICOTINAMIDE, IN PRESENCE OF ALCOHOL OR ALKOXY COMPOUND AND A HYDROXIDE TRAPPING AGENT OR BASE PFIZER INC. 2004-10-26 US disclosed
US-6756373-B1 SUCH AS 5-(2-BUTOXY-5-IODO-3-PYRIDINYL)-3-ETHYL-2-(2-METHOXY-ETHYL)-2,6-DIHYDRO-7H -PYRAZOLO(4,3-D)PYRIMIDIN-7-ONE; CYCLIC GUANOSINE 3',5'-MONOPHOSPHATE PHOSPHODIESTERASE INHIBITORS; ERECTILE DYSFUNCTION PFIZER INC. 2004-06-29 US disclosed
US-20020038024-A1 Process for the preparation of pyrazolo[4,3-d]pyrimidin-7-one compounds and intermediates thereof PFIZER INC. 2002-03-28 US disclosed
EP-1176147-A1 Process for the preparation of pyrazolo[4,3-d]pyrimidin-7-ones and intermediates thereof Pfizer Limited (GB) 2002-01-30 EP 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 (2 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-20020038024-A1 Process for the preparation of pyrazolo[4,3-d]pyrimidin-7-one compounds and intermediates thereof DPYD, HPRT1, SAMHD1 TERT 385/4885SMN1; SMN2 2390/4885MAPT 4371/4885
US-20050143367-A1 Process for the preparation of pyrazolo[4,3-d]pyrimidin-7-one compounds and intermediates thereof NOX4, VKORC1, DPYD TERT 685/4885SMN1; SMN2 2682/4885MAPT 4378/4885

“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.