Nitric Acid

Nitric Acid

SCHEMBL6033717

N=C(N)Nc1ccc(OCCn2cncn2)cc1.O=[N+]([O-])O

nearest known ligand 0.54

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 18)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 5/20 0.51
MAPT P10636 5/20 0.51
ALDH1A1 P00352 5/20 0.51
LMNA P02545 3/20 0.47
NPC1 O15118 3/20 0.47
RAB9A P51151 3/20 0.47
TBXAS1 P24557 1/20 0.45
PKM P14618 1/20 0.44
TP53 P04637 3/20 0.43
TSHR P16473 1/20 0.43
KDM4E B2RXH2 3/20 0.43
MEN1 O00255 2/20 0.43
KMT2A Q03164 2/20 0.43
EGFR P00533 1/20 0.43
NFKB1 P19838 1/20 0.41
NFKB2 Q00653 1/20 0.41
RELA Q04206 1/20 0.41
HPGD P15428 1/20 0.41

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 0.83 ADRB3 (0.39) SMN1; SMN2MAPTALDH1A1LMNAPKM
Nitric Acid SCHEMBL6034079 0.82 TBXAS1 (0.46) MAPTALDH1A1LMNATBXAS1MEN1
Nitric Acid SCHEMBL6034193 0.81 TBXAS1 (0.69) ALDH1A1LMNATBXAS1KDM4EMEN1
Nitric Acid SCHEMBL6033955 0.80 TBXAS1 (0.45) MAPTALDH1A1TBXAS1MEN1KMT2A
Nitric Acid SCHEMBL6033724 0.80 SMN1; SMN2 (0.53) SMN1; SMN2MAPTALDH1A1LMNANPC1
Nitric Acid SCHEMBL6033973 0.77 MAPT (0.47) MAPTALDH1A1LMNANPC1RAB9A
SCHEMBL5656114 0.76 SMN1; SMN2 (0.63) SMN1; SMN2MAPTALDH1A1LMNANPC1
Nitric Acid SCHEMBL6033797 0.75 FBP1 (0.49) SMN1; SMN2MAPTALDH1A1RAB9AKDM4E
Nitric Acid SCHEMBL6033843 0.73 HRH3 (0.54) SMN1; SMN2MAPTALDH1A1KDM4E
Nitric Acid SCHEMBL7232747 0.73 HRH3 (0.54) SMN1; SMN2MAPTALDH1A1KDM4E

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 SMN1; SMN2 3158/4885MAPT 3073/4885ALDH1A1 873/4885
US-20020147339-A1 5-cyano-2-aminopyrimidine derivatives FLT1, FGFR1, KDR SMN1; SMN2 3224/4885MAPT 3079/4885ALDH1A1 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.