Nitric Acid

Nitric Acid

SCHEMBL7240334

COc1cc(N=C(N)N)cc(OC)c1OCCO.O=[N+]([O-])O

nearest known ligand 0.44

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
HTR3E A5X5Y0 1/20 0.44
HTR3B O95264 1/20 0.44
HTR3A P46098 1/20 0.44
HTR3D Q70Z44 1/20 0.44
HTR3C Q8WXA8 1/20 0.44
TUBB1 Q9H4B7 2/20 0.39
TLR4 O00206 4/20 0.37
CD14 P08571 4/20 0.37
LY96 Q9Y6Y9 4/20 0.37
BRD4 O60885 1/20 0.36
CHEK1 O14757 1/20 0.35
PKM P14618 1/20 0.35
SMN1; SMN2 Q16637 2/20 0.35
ALDH1A1 P00352 1/20 0.35
CHUK O15111 1/20 0.35
DAPK3 O43293 1/20 0.35
JAK2 O60674 1/20 0.35
ROCK2 O75116 1/20 0.35
PRKCG P05129 1/20 0.35
CDK1 P06493 1/20 0.35

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 SCHEMBL6980748 0.84 HTR3E (0.53) HTR3EHTR3BHTR3AHTR3DHTR3C
Nitric Acid SCHEMBL7002143 0.80 HTR3E (0.47) HTR3EHTR3BHTR3AHTR3DHTR3C
Nitric Acid SCHEMBL7240326 0.77 L3MBTL1 (0.38) TUBB1BRD4CHEK1PKMSMN1; SMN2
SCHEMBL1326022 0.76 TDP1 (0.49) TUBB1BRD4CHEK1PKMSMN1; SMN2
Nitric Acid SCHEMBL6955447 0.76 HTR3E (0.77) HTR3EHTR3BHTR3AHTR3DHTR3C
Nitric Acid SCHEMBL6034669 0.73 FURIN (0.63) HTR3EHTR3BHTR3AHTR3DHTR3C
SCHEMBL6957365 0.73 HTR3E (0.66) HTR3EHTR3BHTR3AHTR3DHTR3C
Nitric Acid SCHEMBL6953528 0.72 HTR3E (0.53) HTR3EHTR3BHTR3AHTR3DHTR3C
SCHEMBL1327532 0.70 TUBB1 (0.46) TUBB1BRD4SMN1; SMN2ALDH1A1MAPT
Nitric Acid SCHEMBL2910175 0.70 HTR3E (0.61) HTR3EHTR3BHTR3AHTR3DHTR3C

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
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