Nitric Acid

Nitric Acid

SCHEMBL6033797

N=C(N)Nc1ccc(-n2cncn2)cc1.O=[N+]([O-])O

nearest known ligand 0.49

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 16)

geneUniProtsupporting neighboursconfidence
FBP1 P09467 1/20 0.49
KDM4E B2RXH2 3/20 0.44
ALDH1A1 P00352 2/20 0.44
SMN1; SMN2 Q16637 1/20 0.44
MAPT P10636 3/20 0.42
KMT2A Q03164 2/20 0.42
POLB P06746 1/20 0.42
ROCK1 Q13464 1/20 0.40
SYK P43405 2/20 0.40
RAB9A P51151 1/20 0.38
RXFP1 Q9HBX9 1/20 0.38
GPR119 Q8TDV5 1/20 0.38
HPGD P15428 1/20 0.37
MAPK10 P53779 1/20 0.37
SMYD3 Q9H7B4 1/20 0.37
DPP4 P27487 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
Nitric Acid SCHEMBL6033166 0.78 ADRB3 (0.39) KDM4EALDH1A1SMN1; SMN2MAPTKMT2A
SCHEMBL1041509 0.77 ALDH1A1 (0.47) FBP1KDM4EALDH1A1SMN1; SMN2MAPT
Nitric Acid SCHEMBL6033192 0.77 MAPT (0.47) ALDH1A1SMN1; SMN2MAPTKMT2ARAB9A
Nitric Acid SCHEMBL6033904 0.77 NOTUM (0.44) KDM4EALDH1A1SMN1; SMN2KMT2ARAB9A
Nitric Acid SCHEMBL6033802 0.77 FBP1 (0.50) FBP1KDM4EALDH1A1SMN1; SMN2MAPT
Nitric Acid SCHEMBL6033717 0.75 SMN1; SMN2 (0.51) KDM4EALDH1A1SMN1; SMN2MAPTKMT2A
SCHEMBL1165268 0.75 SMN1; SMN2 (0.53) FBP1KDM4EALDH1A1SMN1; SMN2MAPT
SCHEMBL14609432 0.73 ROCK1 (0.45) KDM4EALDH1A1SMN1; SMN2MAPTKMT2A
Nitric Acid SCHEMBL2852035 0.73 PEPD (0.52) KDM4EALDH1A1MAPTKMT2A
Nitric Acid SCHEMBL4613840 0.71 ALDH1A1 (0.53) ALDH1A1SMN1; SMN2MAPTKMT2APOLB

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 FBP1 782/4885KDM4E 2547/4885ALDH1A1 873/4885
US-20020147339-A1 5-cyano-2-aminopyrimidine derivatives FLT1, FGFR1, KDR FBP1 876/4885KDM4E 2566/4885ALDH1A1 859/4885

“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.