Nitric Acid

Nitric Acid

SCHEMBL7265166

N=C(N)Nc1cccc(CCO)c1.O=[N+]([O-])O

nearest known ligand 0.47

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
SIRT1 Q96EB6 1/20 0.47
ITGB3 P05106 1/20 0.44
ITGA2B P08514 1/20 0.44
TRPV1 Q8NER1 3/20 0.43
ALDH1A1 P00352 2/20 0.40
PYGL P06737 1/20 0.40
SMN1; SMN2 Q16637 2/20 0.40
GRIN2D O15399 1/20 0.39
GRIN3B O60391 1/20 0.39
GRIN1 Q05586 1/20 0.39
GRIN2A Q12879 1/20 0.39
GRIN2B Q13224 1/20 0.39
GRIN2C Q14957 1/20 0.39
GRIN3A Q8TCU5 1/20 0.39
SIGMAR1 Q99720 1/20 0.39
ABCG2 Q9UNQ0 1/20 0.39
MEN1 O00255 2/20 0.39
KMT2A Q03164 2/20 0.39
AOC3 Q16853 1/20 0.39
NPC1 O15118 1/20 0.39

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 SCHEMBL1185253 1.00 SIRT1 (0.47) SIRT1ITGB3ITGA2BTRPV1ALDH1A1
SCHEMBL1184796 0.90 SIRT1 (0.51) SIRT1ITGB3ITGA2BTRPV1PYGL
[3-(Hydroxymethyl)Phenyl]Guanidine SCHEMBL5355312 0.89 TRPV1 (0.48) ITGB3ITGA2BTRPV1ALDH1A1SMN1; SMN2
Hydrochloric Acid SCHEMBL538619 0.88 SIRT1 (0.50) SIRT1ITGB3ITGA2BTRPV1PYGL
SCHEMBL18980991 0.84 SIRT1 (0.48) SIRT1ITGB3ITGA2BTRPV1ALDH1A1
Nitric Acid SCHEMBL2076135 0.82 TSHR (0.49) ALDH1A1SMN1; SMN2MEN1KMT2AALOX12
Nitric Acid SCHEMBL27716568 0.81 MAPT (0.42) ITGB3ITGA2BTRPV1ALDH1A1SMN1; SMN2
Nitric Acid SCHEMBL1185784 0.81 MAPT (0.42) ITGB3ITGA2BTRPV1ALDH1A1SMN1; SMN2
Nitric Acid SCHEMBL2073972 0.79 SMN1; SMN2 (0.44) ALDH1A1SMN1; SMN2MEN1KMT2AAOC3
Nitric Acid SCHEMBL2075832 0.78 KMT2A (0.53) TRPV1ALDH1A1SMN1; SMN2GRIN2DGRIN3B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
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

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-20020147339-A1 5-cyano-2-aminopyrimidine derivatives FLT1, FGFR1, KDR SIRT1 1749/4885ITGB3 1315/4885ITGA2B 1937/4885

“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.