Nitric Acid

Nitric Acid

SCHEMBL1993584

CC(C)(C(O)CC(c1ccccc1)C(C)(C)[N+](=O)[O-])[N+](=O)[O-].O=[N+]([O-])O.O=[N+]([O-])O

nearest known ligand 0.41

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 19)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 5/20 0.41
KDM4E B2RXH2 1/20 0.41
CYP3A4 P08684 1/20 0.36
SLC6A2 P23975 2/20 0.36
SLC6A4 P31645 2/20 0.36
SLC6A3 Q01959 2/20 0.36
GSR P00390 1/20 0.36
RIPK1 Q13546 1/20 0.35
LMNA P02545 2/20 0.33
ATM Q13315 1/20 0.32
L3MBTL1 Q9Y468 1/20 0.32
AOC3 Q16853 1/20 0.32
HPGD P15428 2/20 0.32
KMT2A Q03164 2/20 0.32
MEN1 O00255 1/20 0.32
NPC1 O15118 1/20 0.31
ADAM17 P78536 1/20 0.31
MAPT P10636 1/20 0.31
TRPA1 O75762 1/20 0.31

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
SCHEMBL1979844 0.97 ALDH1A1 (0.43) ALDH1A1KDM4ECYP3A4SLC6A2SLC6A4
SCHEMBL1993585 0.90 GSR (0.39) ALDH1A1KDM4ECYP3A4SLC6A2SLC6A4
SCHEMBL13271383 0.77 GSR (0.41) ALDH1A1KDM4ECYP3A4GSRRIPK1
SCHEMBL4443813 0.76 KMT2A (0.47) ALDH1A1KDM4ECYP3A4GSRHPGD
SCHEMBL443077 0.74 ALDH1A1 (0.69) ALDH1A1KDM4ESLC6A2SLC6A4SLC6A3
SCHEMBL14376038 0.74 ALDH1A1 (0.39) ALDH1A1KDM4ECYP3A4GSRRIPK1
Nitric Acid SCHEMBL2006085 0.71 ALDH1A1 (0.35) ALDH1A1KDM4ELMNA
Nitric Acid SCHEMBL1979549 0.71 ALDH1A1 (0.35) ALDH1A1KDM4ELMNA
SCHEMBL11868344 0.69 ALDH1A1 (0.49) ALDH1A1KDM4ELMNAKMT2AMEN1
Phenyl Ethanol SCHEMBL9453901 0.68 LMNA (0.43) ALDH1A1KDM4ECYP3A4GSRLMNA

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-2348073-A1 Use of diamino-alcohol compouds in high solids mineral slurries Dow Global Technologies LLC (US) 2011-07-27 EP disclosed
EP-2341093-A1 Novel diamino-alcohol compounds, their manufacture and use in epoxy resins Dow Global Technologies LLC (US) 2011-07-06 EP disclosed
EP-2338872-A2 Diamino-alcohol compounds and processes for their manufacture Dow Global Technologies LLC (US) 2011-06-29 EP disclosed
EP-2338941-A1 Novel diamino-alcohol compounds, their manufacture and use in coatings applications Dow Global Technologies LLC (US) 2011-06-29 EP disclosed
US-20110147649-A1 Novel diamino-alcohol compounds, their manufacture and use in high solids mineral slurries ADVANCION CORPORATION 2011-06-23 US disclosed
US-20110152574-A1 Novel diamino-alcohol compounds and processes for their manufacture ADVANCION CORPORATION 2011-06-23 US 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 (1 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-20110152574-A1 Novel diamino-alcohol compounds and processes for their manufacture ADH1A, ADH1C, ADH5 ALDH1A1 16/4885KDM4E 542/4885CYP3A4 1327/4885

“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.