Nitric Acid

Nitric Acid

SCHEMBL6033166

N=C(N)Nc1ccc(CCn2cncn2)cc1.O=[N+]([O-])O

nearest known ligand 0.39

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
ADRB3 P13945 1/20 0.39
SMN1; SMN2 Q16637 2/20 0.37
ALDH1A1 P00352 2/20 0.37
MGLL Q99685 1/20 0.36
KMT2A Q03164 2/20 0.36
CYP19A1 P11511 1/20 0.36
HDAC1 Q13547 1/20 0.36
HDAC6 Q9UBN7 1/20 0.36
FLT1 P17948 1/20 0.35
KDR P35968 1/20 0.35
PKM P14618 1/20 0.35
LMNA P02545 1/20 0.34
EGLN3 Q9H6Z9 1/20 0.34
CYP1A2 P05177 1/20 0.34
CYP3A4 P08684 1/20 0.34
CYP2D6 P10635 1/20 0.34
CYP2C19 P33261 1/20 0.34
KDM4E B2RXH2 1/20 0.34
MAPT P10636 1/20 0.34
HPGD P15428 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 SCHEMBL6033717 0.83 SMN1; SMN2 (0.51) SMN1; SMN2ALDH1A1KMT2APKMLMNA
Nitric Acid SCHEMBL6033169 0.79 PLAU (0.41) SMN1; SMN2ALDH1A1PKMLMNAEGLN3
Nitric Acid SCHEMBL6033797 0.78 FBP1 (0.49) SMN1; SMN2ALDH1A1KMT2AKDM4EMAPT
Nitric Acid SCHEMBL2076135 0.76 TSHR (0.49) SMN1; SMN2ALDH1A1KMT2AHDAC6LMNA
SCHEMBL6034201 0.74 CYP19A1 (0.57) KMT2ACYP19A1PKM
SCHEMBL10786317 0.69 CYP19A1 (0.51) SMN1; SMN2ALDH1A1CYP19A1HDAC1HDAC6
Nitric Acid SCHEMBL6033192 0.69 MAPT (0.47) SMN1; SMN2ALDH1A1KMT2ALMNACYP3A4
SCHEMBL3785285 0.68 AOC3 (0.45) CYP3A4CYP2D6
Hydrochloric Acid SCHEMBL29006841 0.68 CYP19A1 (0.50) SMN1; SMN2ALDH1A1CYP19A1HDAC1HDAC6
Nitric Acid SCHEMBL2852035 0.68 PEPD (0.52) ALDH1A1KMT2APKMLMNACYP3A4

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 ADRB3 290/4885SMN1; SMN2 3158/4885ALDH1A1 873/4885
US-20020147339-A1 5-cyano-2-aminopyrimidine derivatives FLT1, FGFR1, KDR ADRB3 259/4885SMN1; SMN2 3224/4885ALDH1A1 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.