Nitric Acid

Nitric Acid

SCHEMBL6034740

N=C(N)Nc1ccc(F)c(C(F)(F)F)c1.O=[N+]([O-])O

nearest known ligand 0.47

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
AR P10275 5/20 0.47
GRM4 Q14833 1/20 0.46
CYP3A4 P08684 2/20 0.43
CES2 O00748 1/20 0.43
ABCB11 O95342 1/20 0.43
ALDH1A1 P00352 1/20 0.43
LMNA P02545 1/20 0.43
CYP1A2 P05177 1/20 0.43
GLA P06280 1/20 0.43
ADORA3 P0DMS8 1/20 0.43
CHRM1 P11229 1/20 0.43
CYP2C9 P11712 1/20 0.43
ALOX15 P16050 1/20 0.43
TSHR P16473 1/20 0.43
TBXA2R P21731 1/20 0.43
AADAC P22760 1/20 0.43
MAPK1 P28482 1/20 0.43
CYP2C19 P33261 1/20 0.43
ADRA1A P35348 1/20 0.43
HTT P42858 1/20 0.43

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 SCHEMBL6034732 1.00 AR (0.47) ARGRM4CYP3A4CES2ABCB11
Nitric Acid SCHEMBL4482314 0.85 KDR (0.58) GRM4ALDH1A1LMNAHTTKDR
Nitric Acid SCHEMBL4467542 0.84 RAB9A (0.44) ALDH1A1LMNACYP1A2TSHRCYP2C19
Nitric Acid SCHEMBL4467551 0.84 RAB9A (0.44) ALDH1A1LMNACYP1A2TSHRCYP2C19
SCHEMBL10384180 0.81 AR (0.47) ARGRM4CYP3A4CES2ABCB11
Nitric Acid SCHEMBL27482170 0.80 MEN1 (0.51) ALDH1A1LMNATSHRHTTSMN1; SMN2
Nitric Acid SCHEMBL6034251 0.80 MEN1 (0.51) ALDH1A1LMNATSHRHTTSMN1; SMN2
Nitric Acid SCHEMBL3859433 0.80 LMNA (0.58) ALDH1A1LMNACYP1A2MAPK1CYP2C19
Nitric Acid SCHEMBL2856189 0.78 KIF11 (0.53) SMN1; SMN2
SCHEMBL1380778 0.77 AR (0.58) ARGRM4ALDH1A1CDK8SLC22A12

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 AR 225/4885GRM4 3604/4885CYP3A4 985/4885
US-20020147339-A1 5-cyano-2-aminopyrimidine derivatives FLT1, FGFR1, KDR AR 258/4885GRM4 3434/4885CYP3A4 939/4885

“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.