Nitric Acid

Nitric Acid

SCHEMBL6033955

N=C(N)Nc1ccc(OCCn2ccnn2)cc1.O=[N+]([O-])O

nearest known ligand 0.45

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 12)

geneUniProtsupporting neighboursconfidence
TBXAS1 P24557 5/20 0.45
MAPT P10636 3/20 0.38
CYP19A1 P11511 1/20 0.38
PDGFRB P09619 2/20 0.37
ATP4A P20648 1/20 0.35
ATP4B P51164 1/20 0.35
MEN1 O00255 3/20 0.34
KMT2A Q03164 3/20 0.34
POLB P06746 1/20 0.34
GAA P10253 1/20 0.34
THRB P10828 1/20 0.34
ALDH1A1 P00352 1/20 0.34

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 SCHEMBL6034079 0.82 TBXAS1 (0.46) TBXAS1MAPTMEN1KMT2AGAA
Nitric Acid SCHEMBL6034193 0.81 TBXAS1 (0.69) TBXAS1MEN1KMT2AALDH1A1
Nitric Acid SCHEMBL6033717 0.80 SMN1; SMN2 (0.51) TBXAS1MAPTMEN1KMT2AALDH1A1
Nitric Acid SCHEMBL6033962 0.80 FURIN (0.48) TBXAS1CYP19A1ATP4AATP4B
Nitric Acid SCHEMBL6033973 0.77 MAPT (0.47) MAPTMEN1KMT2APOLBGAA
SCHEMBL6034573 0.76 LTA4H (0.51) MAPTALDH1A1
Nitric Acid SCHEMBL6033904 0.76 NOTUM (0.44) CYP19A1MEN1KMT2AALDH1A1
Nitric Acid SCHEMBL7232747 0.73 HRH3 (0.54) MAPTPOLBALDH1A1
Nitric Acid SCHEMBL6033843 0.73 HRH3 (0.54) MAPTPOLBALDH1A1
Nitric Acid SCHEMBL7232743 0.73 HRH3 (0.54) MAPTPOLBALDH1A1

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 TBXAS1 296/4885MAPT 3073/4885CYP19A1 350/4885
US-20020147339-A1 5-cyano-2-aminopyrimidine derivatives FLT1, FGFR1, KDR TBXAS1 282/4885MAPT 3079/4885CYP19A1 371/4885

“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.