Nitric Acid

Nitric Acid

SCHEMBL6033845

NC(N)=Nc1ccc(F)cc1F.O=[N+]([O-])O

nearest known ligand 0.44

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ERG11

The experimentally established mechanism targets of Nitric Acid. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ATM Q13315 1/20 0.44
TDP1 Q9NUW8 1/20 0.44
PLAU P00749 3/20 0.44
SLC22A2 O15244 1/20 0.40
SLC22A1 O15245 1/20 0.40
SLC22A3 O75751 1/20 0.40
GRIN2D O15399 2/20 0.39
GRIN3B O60391 2/20 0.39
GRIN1 Q05586 2/20 0.39
GRIN2A Q12879 2/20 0.39
GRIN2B Q13224 2/20 0.39
GRIN2C Q14957 2/20 0.39
GRIN3A Q8TCU5 2/20 0.39
HSPB1 P04792 3/20 0.36
IDO1 P14902 1/20 0.36
TDO2 P48775 1/20 0.36
CES2 O00748 1/20 0.35
CES1 P23141 1/20 0.35
F2 P00734 1/20 0.35
PRSS1 P07477 1/20 0.35

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
SCHEMBL11881011 0.88 SLC22A2 (0.50) PLAUSLC22A2SLC22A1SLC22A3GRIN2D
SCHEMBL11880304 0.80 PLAU (0.54) PLAUGRIN2DGRIN3BGRIN1GRIN2A
SCHEMBL11879125 0.80 PLAU (0.60) ATMTDP1PLAUSLC22A2SLC22A1
Nitric Acid SCHEMBL6970026 0.79 PLAU (0.59) PLAUSLC22A2SLC22A1SLC22A3GRIN2D
Nitric Acid SCHEMBL4613845 0.75 PLAU (0.73) TDP1PLAUSLC22A2SLC22A1SLC22A3
Nitric Acid SCHEMBL1363670 0.73 HTR3E (0.48) PLAUSLC22A2SLC22A1SLC22A3PRSS1
Nitric Acid SCHEMBL6034777 0.72 PLAU (0.53) TDP1PLAUSLC22A2SLC22A1SLC22A3
SCHEMBL11880619 0.72 SLC22A2 (0.50) TDP1PLAUSLC22A2SLC22A1SLC22A3
Nitric Acid SCHEMBL6033747 0.72 PLAU (0.47) PLAUSLC22A2SLC22A1SLC22A3CES2
Nitric Acid SCHEMBL6034160 0.72 PLAU (0.47) PLAUSLC22A2SLC22A1SLC22A3ADRA2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1187816-B1 5-CYANO-2-AMINOPYRIMIDINE DERIVATIVES CELLTECH R&D LTD (GB) 2006-12-20 EP disclosed
US-20040180914-A1 5-Cyano-2-aminopyrimidine derivatives CELLTECH R&D LIMTIED 2004-09-16 US disclosed
US-6579983-B1 Potent and selective inhibitors of receptor tyrosine kinases involved in angiogenesis, especially KDR kinase and/or FGFr kinase CELLTECH R&D LIMITED (GB) 2003-06-17 US disclosed
US-20020147339-A1 5-cyano-2-aminopyrimidine derivatives CELLTECH R&D LIMITED (GB) 2002-10-10 US disclosed
EP-1187816-A1 5-CYANO-2-AMINOPYRIMIDINE DERIVATIVES Celltech R&D Limited (GB) 2002-03-20 EP disclosed
WO-2000078731-A1 5-CYANO-2-AMINOPYRIMIDINE DERIVATIVES CELLTECH R&D LIMITED (GB) 2000-12-28 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 (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-20040180914-A1 5-Cyano-2-aminopyrimidine derivatives FLT1, FGFR1, KDR ATM 976/4885TDP1 1237/4885PLAU 3039/4885
US-20020147339-A1 5-cyano-2-aminopyrimidine derivatives FLT1, FGFR1, KDR ATM 1097/4885TDP1 1231/4885PLAU 3100/4885

“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.