Nitric Acid

Nitric Acid

SCHEMBL4479271

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

nearest known ligand 0.61

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
ALDH1A1 P00352 4/20 0.55
MAPT P10636 6/20 0.53
HTT P42858 2/20 0.53
LMNA P02545 2/20 0.53
PKM P14618 1/20 0.53
MEN1 O00255 3/20 0.52
KMT2A Q03164 3/20 0.52
RAB9A P51151 1/20 0.52
IDO1 P14902 1/20 0.51
KIF11 P52732 2/20 0.51
GAA P10253 2/20 0.50
NPSR1 Q6W5P4 2/20 0.50
TDP1 Q9NUW8 1/20 0.50
TP53 P04637 1/20 0.50
TRPV1 Q8NER1 1/20 0.49
KCNMA1 Q12791 1/20 0.49
PTGS1 P23219 1/20 0.49
XBP1 P17861 1/20 0.49
GRIK1 P39086 1/20 0.48
CA12 O43570 1/20 0.48

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 SCHEMBL5732960 0.94 ALDH1A1 (0.49) ALDH1A1MAPTHTTLMNAPKM
SCHEMBL1999954 0.89 ALDH1A1 (0.61) ALDH1A1MAPTHTTLMNAPKM
Bicarbonate SCHEMBL7469511 0.87 MAPT (0.65) ALDH1A1MAPTHTTLMNAPKM
Nitric Acid SCHEMBL4476163 0.85 P2RX1 (0.48) MAPTLMNARAB9ANPSR1CA12
Nitric Acid SCHEMBL2856189 0.82 KIF11 (0.53) MAPTRAB9AKIF11TRPV1PTGS1
Nitric Acid SCHEMBL20984560 0.82 ALDH1A1 (0.56) ALDH1A1MAPTHTTLMNAPKM
Nitric Acid SCHEMBL1363668 0.81 MEN1 (0.50) ALDH1A1MAPTHTTLMNAPKM
Nitric Acid SCHEMBL6033233 0.81 MEN1 (0.50) ALDH1A1MAPTHTTLMNAPKM
SCHEMBL10384367 0.80 MAPT (0.52) ALDH1A1MAPTHTTLMNAMEN1
Nitric Acid SCHEMBL1590 0.80 MAPT (0.50) ALDH1A1MAPTHTTLMNAMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7582630-B2 Pyradazine compounds as GSK-3 inhibitors SMITHKLINE BEECHAM CORPORATION (US) 2009-09-01 US disclosed
EP-1187816-B1 5-CYANO-2-AMINOPYRIMIDINE DERIVATIVES CELLTECH R&D LTD (GB) 2006-12-20 EP disclosed
EP-0672042-B1 PHARMACOLOGICALLY ACTIVE PYRIMIDINEAMINE DERIVATIVES AND PROCESSES FOR THE PREPARATION THEREOF NOVARTIS AG (CH) 2006-05-03 EP disclosed
US-20060069097-A1 Pyradazine compounds as gsk-3 inhibitors SMITHKLINE BEECHAM CORPORATION 2006-03-30 US disclosed
EP-1551842-A1 PYRADAZINE COMPOUNDS AS GSK-3 INHIBITORS SMITHKLINE BEECHAM CORPORATION (US) 2005-07-13 EP disclosed
US-20040180914-A1 5-Cyano-2-aminopyrimidine derivatives CELLTECH R&D LIMTIED 2004-09-16 US disclosed
WO-2004035588-A1 PYRADAZINE COMPOUNDS AS GSK-3 INHIBITORS SMITHKLINE BEECHAM CORPORATION (US) 2004-04-29 WO 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-0672041-B1 PHARMACOLOGICALLY ACTIVE PYRIDINE DERIVATIVES AND PROCESSES FOR THE PREPARATION THEREOF NOVARTIS AG (CH) 2001-11-14 EP disclosed
CN-1047776-C Pharmacologically active pyridine derivatives and processes for the preparation thereof NOVARTIS AG (CH) 1999-12-29 CN disclosed
US-5728708-A ANTITUMOR AGENTS NOVARTIS CORPORATION (US) 1998-03-17 US disclosed
US-5705502-A Pharmacologically active pyrimidineamine derivatives and processes for the preparation thereof NOVARTIS CORPORATION (US) 1998-01-06 US disclosed
CN-1115982-A pyridine derivatives having pharmacological activity and preparation method thereof CIBA GEIGY AG (CH) 1996-01-31 CN disclosed
EP-0672042-A1 PHARMACOLOGICALLY ACTIVE PYRIMIDINEAMINE DERIVATIVES AND PROCESSES FOR THE PREPARATION THEREOF Novartis AG (CH) 1995-09-20 EP disclosed
EP-0672041-A1 PHARMACOLOGICALLY ACTIVE PYRIDINE DERIVATIVES AND PROCESSES FOR THE PREPARATION THEREOF Novartis AG (CH) 1995-09-20 EP disclosed
WO-1995009851-A1 PHARMACOLOGICALLY ACTIVE PYRIMIDINEAMINE DERIVATIVES AND PROCESSES FOR THE PREPARATION THEREOF CIBA-GEIGY AG (CH) 1995-04-13 WO disclosed
WO-1995009853-A1 PHARMACOLOGICALLY ACTIVE PYRIDINE DERIVATIVES AND PROCESSES FOR THE PREPARATION THEREOF CIBA-GEIGY AG (CH) 1995-04-13 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 (3 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 ALDH1A1 873/4885MAPT 3073/4885HTT 3078/4885
US-20020147339-A1 5-cyano-2-aminopyrimidine derivatives FLT1, FGFR1, KDR ALDH1A1 859/4885MAPT 3079/4885HTT 3148/4885
US-20060069097-A1 Pyradazine compounds as gsk-3 inhibitors GSK3B, GSK3A, GSKIP ALDH1A1 4212/4885MAPT 461/4885HTT 3314/4885

“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.