SCHEMBL588588

SCHEMBL588588

Cc1c2ccc([N+](=O)[O-])cc2nn1C

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 8/20 0.53
CHEK1 O14757 1/20 0.50
DAPK3 O43293 1/20 0.50
GRK5 P34947 1/20 0.50
LIMK1 P53667 1/20 0.50
ALDH1A1 P00352 4/20 0.49
POLB P06746 2/20 0.49
MEN1 O00255 3/20 0.46
KMT2A Q03164 3/20 0.46
SMN1; SMN2 Q16637 3/20 0.46
L3MBTL1 Q9Y468 2/20 0.46
NPC1 O15118 2/20 0.46
LMNA P02545 2/20 0.46
RAB9A P51151 2/20 0.46
NFKB1 P19838 1/20 0.46
CASP3 P42574 1/20 0.46
NFKB2 Q00653 1/20 0.46
RELA Q04206 1/20 0.46
SENP8 Q96LD8 1/20 0.46
SENP7 Q9BQF6 1/20 0.46

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
SCHEMBL22473631 0.83 MAPT (0.51) MAPTALDH1A1POLBMEN1KMT2A
SCHEMBL28996878 0.83 MAPT (0.51) MAPTALDH1A1POLBMEN1KMT2A
SCHEMBL27546495 0.80 MAPT (0.49) MAPTALDH1A1POLBMEN1KMT2A
SCHEMBL13106368 0.80 MAPT (0.49) MAPTCHEK1DAPK3GRK5LIMK1
SCHEMBL585538 0.79 MAPT (0.48) MAPTALDH1A1POLBMEN1KMT2A
SCHEMBL589194 0.79 MAPT (0.48) MAPTALDH1A1POLBMEN1KMT2A
SCHEMBL27566551 0.79 MAPT (0.48) MAPTALDH1A1POLBMEN1KMT2A
SCHEMBL2842932 0.79 MAPT (0.48) MAPTALDH1A1POLBMEN1KMT2A
SCHEMBL27566549 0.77 MAPT (0.46) MAPTALDH1A1POLBMEN1KMT2A
SCHEMBL2850485 0.76 ELANE (0.47) MAPTALDH1A1POLBMEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114394935-A Improved preparation method of pazopanib key intermediate 南京亿华药业有限公司 2022-04-26 CN claimed
CN-109212042-B Analysis method for determining toxicity impurities of pezopyr hydrochloride gene by adopting liquid chromatography-mass spectrometry 齐鲁制药有限公司 2022-03-04 CN claimed
CN-109212042-A A kind of analysis method using liquid chromatography and mass spectrometry hydrochloric acid training azoles Pa Nijiyin toxic impurities 齐鲁制药有限公司 2019-01-15 CN claimed
EP-2935250-B1 PROCESS FOR THE PREPARATION OF PAZOPANIB OR SALTS THEREOF SUN PHARMACEUTICAL IND LTD (IN) 2018-03-28 EP claimed
US-9802923-B2 Process for the preparation of pazopanib or salts thereof SUN PHARMACEUTICAL INDUSTRIES LIMITED (IN) 2017-10-31 US claimed
CN-103319410-B A kind of synthetic method of indazole compound TIANJIN INSTITUTE OF PHARMACEUTICAL RESEARCH (CN) 2016-04-06 CN claimed
US-20150329526-A1 PROCESS FOR THE PREPARATION OF PAZOPANIB OR SALTS THEREOF SUN PHARMACEUTICAL INDUSTRIES LIMITED (IN) 2015-11-19 US claimed
EP-2935250-A1 PROCESS FOR THE PREPARATION OF PAZOPANIB OR SALTS THEREOF Ranbaxy Laboratories Limited (IN) 2015-10-28 EP claimed
WO-2014097152-A1 PROCESS FOR THE PREPARATION OF PAZOPANIB OR SALTS THEREOF RANBAXY LABORATORIES LIMITED (IN) 2014-06-26 WO claimed
CN-103319410-A Synthesis method of indazole compound TIANJIN INST PHARM RESEARCH 2013-09-25 CN claimed
CN-117924177-A Preparation method of pazopanib intermediate 2, 3-dimethyl-6-amino-2H-indazole and analogues thereof 南京杰运医药科技有限公司 2024-04-26 CN disclosed
US-20240050429-A1 PAZOPANIB PHARMACEUTICAL COMPOSITION, INJECTION AND PREPARATION METHOD AND USE THEREOF Qx Therapeutics, Inc. 2024-02-15 US disclosed
US-20230026808-A1 COMPOUNDS, COMPOSITIONS, AND METHODS FOR TREATING ISCHEMIA-REPERFUSION INJURY AND/OR LUNG INJURY YALE UNIVERSITY 2023-01-26 US disclosed
US-20230026808-A1 COMPOUNDS, COMPOSITIONS, AND METHODS FOR TREATING ISCHEMIA-REPERFUSION INJURY AND/OR LUNG INJURY YALE UNIVERSITY 2023-01-26 US disclosed
US-11427570-B2 Process for the preparation of pazopanib or a pharmaceutically acceptable salt thereof LAURUS LABS LIMITED (IN) 2022-08-30 US disclosed
US-20040242578-A1 Pyrimidineamines as angiogenesis modulators NOVARTIS AG (CH) 2004-12-02 US disclosed
CN-1549813-A Pyrimidinamines as angiogenesis modulators 2004-11-24 CN disclosed
WO-2003106416-A2 CHEMICAL PROCESS SMITHKLINE BEECHAM CORPORATION (US) 2003-12-24 WO disclosed
EP-1343782-A1 PYRIMIDINEAMINES AS ANGIOGENESIS MODULATORS GLAXO GROUP LIMITED (GB) 2003-09-17 EP disclosed
WO-2002059110-A1 PYRIMIDINEAMINES AS ANGIOGENESIS MODULATORS GLAXO GROUP LIMITED (GB) 2002-08-01 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 (4 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-20040242578-A1 Pyrimidineamines as angiogenesis modulators TYMS, TYMP, DPYD MAPT 3924/4885CHEK1 500/4885DAPK3 513/4885
US-20230026808-A1 COMPOUNDS, COMPOSITIONS, AND METHODS FOR TREATING ISCHEMIA-REPERFUSION INJURY AND/OR LUNG INJURY DAPK3, PAK3, MAVS MAPT 585/4885CHEK1 328/4885DAPK3 1/4885
US-11427570-B2 Process for the preparation of pazopanib or a pharmaceutically acceptable salt thereof JAK2, SF3B5, PDGFRB MAPT 4359/4885CHEK1 2277/4885DAPK3 2524/4885
US-20150329526-A1 PROCESS FOR THE PREPARATION OF PAZOPANIB OR SALTS THEREOF ABL1, PDGFRB, PDGFRA MAPT 4012/4885CHEK1 568/4885DAPK3 2494/4885

“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.