Nitric Acid

Nitric Acid

SCHEMBL1717

Cc1ccc([N+](=O)[O-])cc1NC(=N)N.O=[N+]([O-])O

nearest known ligand 0.57

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
HTT P42858 2/20 0.57
SMN1; SMN2 Q16637 2/20 0.57
ALDH1A1 P00352 6/20 0.56
KMT2A Q03164 7/20 0.54
HPGD P15428 4/20 0.53
MAPT P10636 4/20 0.53
POLB P06746 2/20 0.53
LMNA P02545 2/20 0.52
MEN1 O00255 4/20 0.52
CYP1A2 P05177 2/20 0.52
CYP2C9 P11712 2/20 0.52
CYP2C19 P33261 2/20 0.52
ALOX12 P18054 1/20 0.52
L3MBTL1 Q9Y468 1/20 0.52
MAPK1 P28482 1/20 0.50
KAT2B Q92831 1/20 0.50
CYP3A4 P08684 1/20 0.49
CYP2D6 P10635 1/20 0.49
KDM4E B2RXH2 1/20 0.49
CTDSP1 Q9GZU7 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
Nitric Acid SCHEMBL30496141 1.00 HTT (0.57) HTTSMN1; SMN2ALDH1A1KMT2AHPGD
SCHEMBL30078131 0.97 HTT (0.59) HTTSMN1; SMN2ALDH1A1KMT2AHPGD
SCHEMBL1583292 0.97 HTT (0.59) HTTSMN1; SMN2ALDH1A1KMT2AHPGD
Hydrochloric Acid SCHEMBL2930759 0.95 HTT (0.58) HTTSMN1; SMN2ALDH1A1KMT2AHPGD
Nitric Acid SCHEMBL3635730 0.93 CYP3A4 (0.61) HTTSMN1; SMN2ALDH1A1KMT2AHPGD
Sulfuric Acid SCHEMBL21799346 0.92 ALDH1A1 (0.57) HTTSMN1; SMN2ALDH1A1KMT2AHPGD
Nitric Acid SCHEMBL3858360 0.88 GRIN2D (0.60) HTTSMN1; SMN2ALDH1A1KMT2AMAPT
SCHEMBL4107531 0.86 HTT (0.54) HTTSMN1; SMN2ALDH1A1KMT2AHPGD
SCHEMBL11876436 0.85 GRIN2D (0.63) HTTSMN1; SMN2ALDH1A1KMT2AMAPT
SCHEMBL5527561 0.83 HTT (0.65) HTTSMN1; SMN2ALDH1A1KMT2AHPGD

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 124 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118496627-B FRP composite material and preparation method and application thereof 南京斯贝尔复合材料仪征有限公司 2024-10-22 CN claimed
CN-118496627-A FRP composite material and preparation method and application thereof 南京斯贝尔复合材料仪征有限公司 2024-08-16 CN claimed
CN-114790154-B Preparation method of antitumor drug imatinib intermediate (2-methyl-5-nitrophenyl) guanidine nitrate 福建南方制药股份有限公司 2023-12-08 CN claimed
CN-114790154-A Preparation method of antineoplastic drug imatinib intermediate- (2-methyl-5-nitrophenyl) guanidine nitrate 福建南方制药股份有限公司 2022-07-26 CN claimed
CN-112827368-A Anti-pollution reverse osmosis membrane and preparation method thereof 中化(宁波)润沃膜科技有限公司 2021-05-25 CN claimed
CN-111039921-A Synthesis process of imatinib and imatinib mesylate 杭州沧海帆医药科技有限公司 2020-04-21 CN claimed
EP-3333162-A1 METOD FOR PREPARING N-(2-METHYL-5-NITROPHENYL)-4-(PYRIDIN-3-YL)PYRIMIDIN-2-AMINE Silesian Catalysts sp. z o.o. (PL) 2018-06-13 EP claimed
EP-3299358-A1 AMIDE DERIVATIVE AND MEDICINE Nippon Shinyaku Co., Ltd. (JP) 2018-03-28 EP claimed
CN-102911157-B (E)-3-[2-bromo-5-(3-substituted propoxy)]phenyl-N-{4-methyl-3-[4-(pyridin-3-yl)pyrimidin-2-yl]amino}phenyl acrylamide compound UNIV SHENYANG PHARMACEUTICAL 2014-04-02 CN claimed
EP-1833815-B1 A PROCESS FOR PREPARATION OF IMATINIB BASE INST FARMACEUTYCZNY (PL) 2010-09-15 EP claimed
US-7674901-B2 Process for preparation of imatinib base INSTYTUT FARMACEUTYCZNY (PL) 2010-03-09 US claimed
US-20080194819-A1 Process For Preparation of Imatinib Base INSTYTUT FARMACEUTYCZNY (PL) 2008-08-14 US claimed
EP-1833815-A2 A PROCESS FOR PREPARATION OF IMATINIB BASE INSTYTUT FARMACEUTYCZNY (PL) 2007-09-19 EP claimed
WO-2006071130-A2 A PROCESS FOR PREPARATION OF IMATINIB BASE INSTYTUT FARMACEUTYCZNY (PL) 2006-07-06 WO claimed
WO-2004108699-A1 PROCESS FOR THE PREPARATION OF THE ANTI-CANCER DRUG IMATINIB AND ITS ANALOGUES NATCO PHARMA LIMITED (IN) 2004-12-16 WO claimed
CN-118496627-B FRP composite material and preparation method and application thereof 南京斯贝尔复合材料仪征有限公司 2024-10-22 CN disclosed
CN-118496627-A FRP composite material and preparation method and application thereof 南京斯贝尔复合材料仪征有限公司 2024-08-16 CN disclosed
US-5521184-A ANTITUMOR AGENTS; imatinib mesylate CIBA-GEIGY CORPORATION (US) 1996-05-28 US disclosed
CN-1077713-A Pyrimidine derivatives and preparation method thereof CIBA GEIGY AG (CH) 1993-10-27 CN disclosed
EP-0564409-A1 Pyrimidin derivatives and process for their preparation CIBA-GEIGY AG (CH) 1993-10-06 EP 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-20080194819-A1 Process For Preparation of Imatinib Base ABL1, ABL2, JAK2 HTT 2724/4885SMN1; SMN2 1248/4885ALDH1A1 262/4885

“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.