Nitric Acid

Nitric Acid

SCHEMBL3858285

Cc1ccc(NC(=N)N)cc1[N+](=O)[O-].O=[N+]([O-])O

nearest known ligand 0.58

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
KMT2A Q03164 7/20 0.58
MAPT P10636 7/20 0.58
SMN1; SMN2 Q16637 6/20 0.58
RAB9A P51151 6/20 0.58
MEN1 O00255 6/20 0.58
NPC1 O15118 5/20 0.58
LMNA P02545 2/20 0.58
MAPK1 P28482 2/20 0.58
PPIA P62937 1/20 0.56
HPGD P15428 2/20 0.53
ATM Q13315 1/20 0.53
TDP1 Q9NUW8 1/20 0.53
ALOX12 P18054 1/20 0.50
ALDH1A1 P00352 6/20 0.49
NPSR1 Q6W5P4 1/20 0.49
CYP3A4 P08684 1/20 0.49
TSHR P16473 1/20 0.49
RECQL P46063 1/20 0.49

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
SCHEMBL27684440 0.97 KMT2A (0.61) KMT2AMAPTSMN1; SMN2RAB9AMEN1
Nitric Acid SCHEMBL1184604 0.86 POLB (0.49) KMT2AMAPTSMN1; SMN2RAB9AMEN1
Nitric Acid SCHEMBL27716562 0.86 POLB (0.49) KMT2AMAPTSMN1; SMN2RAB9AMEN1
Nitric Acid SCHEMBL27571319 0.84 MAPK1 (0.50) KMT2AMAPTSMN1; SMN2RAB9AMEN1
Nitric Acid SCHEMBL6162457 0.84 MAPK1 (0.50) KMT2AMAPTSMN1; SMN2RAB9AMEN1
SCHEMBL5530308 0.83 KMT2A (0.67) KMT2AMAPTSMN1; SMN2RAB9AMEN1
Nitric Acid SCHEMBL4166394 0.82 ALDH1A1 (0.41) KMT2AMAPTSMN1; SMN2RAB9AMEN1
Nitric Acid SCHEMBL6034482 0.82 NPC1 (0.53) KMT2AMAPTSMN1; SMN2RAB9AMEN1
Nitric Acid SCHEMBL3859433 0.82 LMNA (0.58) KMT2AMAPTSMN1; SMN2RAB9AMEN1
SCHEMBL14662373 0.82 PPIA (0.66) KMT2AMAPTSMN1; SMN2RAB9AMEN1

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
US-7595323-B2 N-phenyl-2-pyrimidine-amine derivatives and process for the preparation thereof IL YANG PHARM. CO., LTD. (KR) 2009-09-29 US disclosed
US-20090137572-A1 2-substituted-4-heteroaryl-pyrimidines useful for the treatment of proliferative disorders CYCLACEL LIMITED (GB) 2009-05-28 US disclosed
EP-1756098-A2 2-SUBSTITUTED-4-HETEROARYL-PYRIMIDINES USEFUL FOR THE TREATMENT OF PROLIFERATIVE DISORDERS Cyclacel Limited (GB) 2007-02-28 EP disclosed
WO-2005116025-A2 2-SUBSTITUTED-4-HETEROARYL-PYRIMIDINES USEFUL FOR THE TREATMENT OF PROLIFERATIVE DISORDERS CYCLACEL LIMITED (GB) 2005-12-08 WO disclosed
US-20040248918-A1 Anticancer agents IL YANG PHARM. CO., LTD. 2004-12-09 US disclosed
WO-2004099186-A1 N-PHENYL-2-PYRIMIDINE-AMINE DERIVATIVES AND PROCESS FOR THE PREPARATION THEREOF IL YANG PHARM CO., LTD. (KR) 2004-11-18 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-20090137572-A1 2-substituted-4-heteroaryl-pyrimidines useful for the treatment of proliferative disorders CDK2, CDK4, CDK20 KMT2A 1239/4885MAPT 2054/4885SMN1; SMN2 2335/4885
US-20040248918-A1 Anticancer agents BRDT, CHIA, RNASE1 KMT2A 73/4885MAPT 833/4885SMN1; SMN2 26/4885

“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.