Nitric Acid

Nitric Acid

SCHEMBL1833741

NC(N)=Nc1ccc(Br)cc1.O=[N+]([O-])O

nearest known ligand 0.73

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
PLAU P00749 5/20 0.73
SLC22A2 O15244 5/20 0.73
SLC22A1 O15245 5/20 0.73
SLC22A3 O75751 5/20 0.73
POLB P06746 1/20 0.54
NOS1 P29475 4/20 0.53
ADRA2A P08913 4/20 0.47
ADRA2B P18089 4/20 0.47
ADRA2C P18825 4/20 0.47
CA12 O43570 3/20 0.47
CA1 P00915 3/20 0.47
CA2 P00918 3/20 0.47
CA9 Q16790 3/20 0.47
GRIN2D O15399 1/20 0.46
GRIN3B O60391 1/20 0.46
GRIN1 Q05586 1/20 0.46
GRIN2A Q12879 1/20 0.46
GRIN2B Q13224 1/20 0.46
GRIN2C Q14957 1/20 0.46
GRIN3A Q8TCU5 1/20 0.46

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
SCHEMBL2447318 0.85 SLC22A2 (1.00) PLAUSLC22A2SLC22A1SLC22A3POLB
Hydrochloric Acid SCHEMBL1115167 0.83 SLC22A2 (0.95) PLAUSLC22A2SLC22A1SLC22A3POLB
Nitric Acid SCHEMBL6033862 0.82 CA12 (0.72) PLAUSLC22A2SLC22A1SLC22A3POLB
Nitric Acid SCHEMBL2544085 0.81 PLAU (0.73) PLAUSLC22A2SLC22A1SLC22A3POLB
Nitric Acid SCHEMBL4613845 0.81 PLAU (0.73) PLAUSLC22A2SLC22A1SLC22A3POLB
Nitric Acid SCHEMBL3860515 0.81 PLAU (0.92) PLAUPOLBNOS1ADRA2AADRA2B
Phenylguanidine SCHEMBL6129042 0.80 PLAU (0.71) PLAUSLC22A2SLC22A1SLC22A3POLB
Nitric Acid SCHEMBL3250038 0.79 HTR3E (0.48) PLAUSLC22A2SLC22A1SLC22A3NOS1
SCHEMBL240459 0.76 PLAU (1.00) PLAUPOLBNOS1ADRA2AADRA2B
Nitric Acid SCHEMBL6033181 0.75 PLAU (0.54) PLAUSLC22A2POLBNOS1ADRA2A

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-2318377-A1 PYRIMIDINE COMPOUNDS, COMPOSITIONS AND METHODS OF USE Genentech, Inc. (US) 2011-05-11 EP disclosed
WO-2010014939-A1 PYRIMIDINE COMPOUNDS, COMPOSITIONS AND METHODS OF USE GENENTECH, INC. (US) 2010-02-04 WO disclosed
US-6599908-B1 Potent and selective inhibitors of the protein tyrosine kinases p56lck and p59fyn CELLTECH R & D LIMITED (GB) 2003-07-29 US disclosed
US-6057329-A Fused polycyclic 2-aminopyrimidine derivatives CELLTECH THERAPEUTICS LIMITED (GB) 2000-05-02 US disclosed
EP-0946523-A1 FUSED POLYCYCLIC 2-AMINOPYRIMIDINE DERIVATIVES, THEIR PREPARATION AND THEIR USE AS PROTEIN TYROSINE KINASE INHIBITORS CELLTECH THERAPEUTICS LIMITED (GB) 1999-10-06 EP disclosed
WO-1998028281-A1 FUSED POLYCYCLIC 2-AMINOPYRIMIDINE DERIVATIVES, THEIR PREPARATION AND THEIR USE AS PROTEIN TYROSINE KINASE INHIBITORS CELLTECH THERAPEUTICS LIMITED (GB) 1998-07-02 WO disclosed