SCHEMBL525877

SCHEMBL525877

O=c1cc(-c2ccccc2)c(=O)[nH][nH]1

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 3/20 0.59
KDM4E B2RXH2 3/20 0.59
GAA P10253 1/20 0.59
TDP1 Q9NUW8 1/20 0.59
PLK4 O00444 1/20 0.50
MAPK9 P45984 1/20 0.50
LIMK1 P53667 1/20 0.50
CLK4 Q9HAZ1 1/20 0.50
AKT3 Q9Y243 1/20 0.50
HPGD P15428 1/20 0.47
MAPK1 P28482 1/20 0.47
HTT P42858 1/20 0.47
SMN1; SMN2 Q16637 1/20 0.47
PARP1 P09874 1/20 0.45
ALDH1A1 P00352 1/20 0.44
NOTUM Q6P988 2/20 0.43
PDE4A P27815 1/20 0.43
PDE4B Q07343 1/20 0.43
PDE4C Q08493 1/20 0.43
PDE4D Q08499 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
SCHEMBL16060851 0.81 PDE3B (0.45) MAPTKDM4EGAATDP1CLK4
SCHEMBL4872103 0.81 GAA (0.60) MAPTKDM4EGAATDP1HTT
SCHEMBL4522255 0.78 GSTP1 (0.60) MAPTKDM4EGAATDP1NOTUM
SCHEMBL1013408 0.77 KIF11 (0.44) PARP1NOTUMBACE1
SCHEMBL3372323 0.74 MAPT (1.00) MAPTKDM4EGAATDP1HPGD
SCHEMBL6798828 0.73 MAPT (0.69) MAPTALDH1A1MEN1KMT2A
SCHEMBL3263382 0.73 ALDH1A1 (0.53) MAPTKDM4EGAATDP1PLK4
SCHEMBL11846035 0.71 MAPT (0.91) MAPTKDM4EGAATDP1HPGD
SCHEMBL2442343 0.69 GSTP1 (0.62) MAPTKDM4EHPGDMAPK1HTT
SCHEMBL1754735 0.68 POLB (0.57) MAPTGAALIMK1CLK4HPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240051925-A1 METHODS FOR PREPARING PYRIDAZINONE DERIVATIVES LSI FINANCING LLC, AS ADMINISTRATIVE AGENT 2024-02-15 US disclosed
EP-4232436-A1 PROCESS FOR THE PREPARATION OF 6-(4-NITRO-PHENOXY)-2H-PYRIDAZIN-3-ONE AND 6-(4-AMINO-PHENOXY)-2H-PYRIDAZIN-3-ONE DERIVATIVES AS INTERMEDIATES OF THYROID HORMONE ANALOGUES Madrigal Pharmaceuticals, Inc. (US) 2023-08-30 EP disclosed
CN-116406356-A Process for the preparation of 6- (4-nitro-phenoxy) -2H-pyridazin-3-one and 6- (4-amino-phenoxy) -2H-pyridazin-3-one derivatives as intermediates for thyroid hormone analogues 马德里加尔制药公司 2023-07-07 CN disclosed
CN-111909137-B Pyridazinone derivative and application thereof 深圳微芯生物科技股份有限公司 2023-05-30 CN disclosed
WO-2022087141-A1 PROCESS FOR THE PREPARATION OF 6-(4-NITRO-PHENOXY)-2H-PYRIDAZIN-3-ONE AND 6-(4-AMINO-PHENOXY)-2H-PYRIDAZIN-3-ONE DERIVATIVES AS INTERMEDIATES OF THYROID HORMONE ANALOGUES MADRIGAL PHARMACEUTICALS, INC. (US) 2022-04-28 WO disclosed
WO-2022087141-A1 PROCESS FOR THE PREPARATION OF 6-(4-NITRO-PHENOXY)-2H-PYRIDAZIN-3-ONE AND 6-(4-AMINO-PHENOXY)-2H-PYRIDAZIN-3-ONE DERIVATIVES AS INTERMEDIATES OF THYROID HORMONE ANALOGUES MADRIGAL PHARMACEUTICALS, INC. (US) 2022-04-28 WO disclosed
WO-2020228577-A1 PYRIDAZINONE DERIVATIVE AND USE THEREOF 深圳微芯生物科技股份有限公司 2020-11-19 WO disclosed
CN-111909137-A Pyridazinone derivative and application thereof 深圳微芯生物科技股份有限公司 2020-11-10 CN disclosed
US-9663493-B2 Pyridazine compounds, compositions and methods NORTHWESTERN UNIVERSITY (US) 2017-05-30 US disclosed
US-9527819-B2 Pyridazine compounds, compositions and methods NORTHWESTERN UNIVERSITY 2016-12-27 US disclosed
US-20080318899-A1 Pyridazine Compounds, Compositions and Methods UNIVERSITE DE STRASBOURG (FR) 2008-12-25 US disclosed
US-20080318899-A1 Pyridazine Compounds, Compositions and Methods UNIVERSITE DE STRASBOURG (FR) 2008-12-25 US disclosed
US-7300932-B2 Pyrrolo[1,2-b]pyridazine derivatives JAPAN TOBACCO INC. (JP) 2007-11-27 US disclosed
US-20060142178-A1 Method of treating cancer BARNETT STANLEY F 2006-06-29 US disclosed
US-20060069110-A1 Substituted heterocyclic compounds and methods of use AMGEN INC. 2006-03-30 US disclosed
US-6960584-B2 Inhibitors of Akt activity MERCK & CO., INC. (US) 2005-11-01 US disclosed
US-20050070545-A1 For treatment or prevention of metabolic and cell proliferative diseases; modifying lipid metabolism TULARIK INC. (US) 2005-03-31 US disclosed
US-20040116432-A1 Inhibitors of akt activity MERCK SHARP & DOHME LTD. (GB) 2004-06-17 US disclosed
US-20040106540-A1 Method of treating cancer BARNETT STANLEY F (US) 2004-06-03 US disclosed
US-20040102360-A1 Combination therapy BARNETT STANLEY F (US) 2004-05-27 US 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 (7 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-20050070545-A1 For treatment or prevention of metabolic and cell proliferative diseases; modifying lipid metabolism PC, ACACB, ACAT1 MAPT 2498/4885KDM4E 2907/4885GAA 278/4885
US-20080318899-A1 Pyridazine Compounds, Compositions and Methods APP, PSEN1, PSEN2 MAPT 32/4885KDM4E 2808/4885GAA 3526/4885
US-20240051925-A1 METHODS FOR PREPARING PYRIDAZINONE DERIVATIVES CYP7A1, LIPC, CYP11B2 MAPT 3117/4885KDM4E 2280/4885GAA 880/4885
US-20060069110-A1 Substituted heterocyclic compounds and methods of use MAPT, MYLK2, IAPP MAPT 1/4885KDM4E 4000/4885GAA 2288/4885
US-20040102360-A1 Combination therapy MTOR, AKT2, PLK1 MAPT 3086/4885KDM4E 2180/4885GAA 1689/4885
US-20060142178-A1 Method of treating cancer PACSIN2, CTTN, TNK2 MAPT 3209/4885KDM4E 2137/4885GAA 1693/4885
US-20040106540-A1 Method of treating cancer PACSIN2, CTTN, PLK1 MAPT 3059/4885KDM4E 2374/4885GAA 1758/4885

“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.