SCHEMBL3264283

SCHEMBL3264283

Cc1cc(=O)[nH]n1-c1ccccc1

nearest known ligand 0.57

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 4/20 0.50
AURKA O14965 1/20 0.49
DAPK3 O43293 1/20 0.49
PDGFRA P16234 1/20 0.49
LTK P29376 1/20 0.49
GRK5 P34947 1/20 0.49
CSNK1A1 P48729 1/20 0.49
CDK8 P49336 1/20 0.49
CDK9 P50750 1/20 0.49
PRKX P51817 1/20 0.49
NEK2 P51955 1/20 0.49
LIMK1 P53667 1/20 0.49
CDK5 Q00535 1/20 0.49
ACVR1 Q04771 1/20 0.49
TYRO3 Q06418 1/20 0.49
PRKAA1 Q13131 1/20 0.49
DYRK1A Q13627 1/20 0.49
IKBKE Q14164 1/20 0.49
LRRK2 Q5S007 1/20 0.49
CLK4 Q9HAZ1 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
SCHEMBL3835955 0.81 ALDH1A1 (0.39) ALDH1A1AURKADAPK3PDGFRALTK
SCHEMBL3261626 0.81 AR (0.39) ALDH1A1AURKADAPK3PDGFRALTK
SCHEMBL3262746 0.80 NPC1 (0.42) ALDH1A1GAALMNAMAPTL3MBTL1
SCHEMBL1114873 0.80 HSP90AA1 (0.46) ALDH1A1GAAPOLBMPINPC1
SCHEMBL3268349 0.79 CYP2E1 (0.46) ALDH1A1GAAMAPTL3MBTL1POLB
SCHEMBL3262867 0.79 ALKBH5 (0.54) ALDH1A1GAAMAPTL3MBTL1POLB
SCHEMBL10373240 0.78 MAPT (0.61) ALDH1A1GAALMNAMAPTL3MBTL1
SCHEMBL29401773 0.77 ALKBH5 (0.51) ALDH1A1AURKADAPK3PDGFRALTK
SCHEMBL13860451 0.76 AURKA (0.57) ALDH1A1AURKADAPK3PDGFRALTK
SCHEMBL31503514 0.76 MEN1 (0.50) ALDH1A1AURKADAPK3PDGFRALTK

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1040817-B1 Dyeing composition comprising a pyrazolo(1,5-a)pyrimidine and a monocyclic polyaminopyrimidine as oxidation bases and a coupler, and dyeing process OREAL (FR) 2005-02-02 EP claimed
CN-108409662-B Hydroxylamine-substituted Meldrum's acid, Barbituric acid and pyrazolone derivatives as HNO donors 约翰斯霍普金斯大学 2021-10-26 CN disclosed
US-9862699-B2 Meldrum's acid, barbituric acid and pyrazolone derivatives substituted with hydroxylamine as HNO donors THE JOHNS HOPKINS UNIVERSITY (US) 2018-01-09 US disclosed
EP-2776402-B1 MELDRUM'S ACID, BARBITURIC ACID AND PYRAZOLONE DERIVATIVES SUBSTITUTED WITH HYDROXYLAMINE AS HNO DONORS UNIV JOHNS HOPKINS (US) 2017-07-26 EP disclosed
US-20170050947-A1 MELDRUM'S ACID, BARBITURIC ACID AND PYRAZOLONE DERIVATIVES SUBSTITUTED WITH HYDROXYLAMINE AS HNO DONORS THE JOHNS HOPKINS UNIVERSITY 2017-02-23 US disclosed
US-9499511-B2 N-substituted hydroxylamine derivatives with carbon-based leaving groups THE JOHNS HOPKINS UNIVERSITY (US) 2016-11-22 US disclosed
US-20160115148-A1 N-SUBSTITUTED HYDROXYLAMINE DERIVATIVES WITH CARBON-BASED LEAVING GROUPS NATIONAL SCIENCE FOUNDATION 2016-04-28 US disclosed
US-9181213-B2 Meldrum's acid, barbituric acid and pyrazolone derivatives substituted with hydroxylamine as HNO donors THE JOHNS HOPKINS UNIVERSITY (US) 2015-11-10 US disclosed
US-20140275134-A1 MELDRUM'S ACID, BARBITURIC ACID AND PYRAZOLONE DERIVATIVES SUBSTITUTED WITH HYDROXYLAMINE AS HNO DONORS NATIONAL SCIENCE FOUNDATION 2014-09-18 US disclosed
CN-104053647-A Hydroxylamine-substituted Meldrum's acid, Barbituric acid and pyrazolone derivatives as HNO donors UNIV JOHNS HOPKINS 2014-09-17 CN disclosed
EP-0415885-A1 Bis-Phthalideactones, process for their preparation, and their use in recording materials CIBA-GEIGY AG (CH) 1991-03-06 EP disclosed
EP-0377406-A1 Pressure-sensitive or heat-sensitive recording material CIBA-GEIGY AG (CH) 1990-07-11 EP disclosed
EP-0373110-A2 Pressure-sensitive or heat-sensitive recording material CIBA-GEIGY AG (CH) 1990-06-13 EP disclosed
US-4933448-A FOR PRESSURE OR HEAT SENSITIVE RECORDING MATERIALS CIBA-GEIGY CORPORATION (US) 1990-06-12 US disclosed
EP-0185909-B1 5-ALKYL-1-PHENYL-2-PIPERAZINO ALKYLPYRAZOLIN-3-ONE COMPOUNDS AS WELL AS PROCESSES AND INTERMEDIATES FOR THEIR PREPARATION AND MEDICAMENTS CONTAINING THESE COMPOUNDS Kali-Chemie Pharma GmbH (DE) 1990-02-21 EP disclosed
EP-0340169-A2 Chromogenic lactone compounds of benzopyrano-2H-pyrazoles CIBA-GEIGY AG (CH) 1989-11-02 EP disclosed
US-4672063-A Antiallergic 5-alkyl-1-phenyl-2-piperazinoalkylpyrazolin-3-one compounds KALI-CHEMIE PHARMA GMBH (DE) 1987-06-09 US disclosed
US-4617258-A WATER SOLUBLE GROUP 8 COMPOUNDS KONISHIROKU PHOTO INDUSTRY CO., LTD. (JP) 1986-10-14 US disclosed
EP-0185909-A1 5-Alkyl-1-phenyl-2-piperazino alkylpyrazolin-3-one compounds as well as processes and intermediates for their preparation and medicaments containing these compounds Kali-Chemie Pharma GmbH (DE) 1986-07-02 EP disclosed
EP-0091788-A2 Silver halide photographic material KONICA CORPORATION (JP) 1983-10-19 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 (3 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-20170050947-A1 MELDRUM'S ACID, BARBITURIC ACID AND PYRAZOLONE DERIVATIVES SUBSTITUTED WITH HYDROXYLAMINE AS HNO DONORS HMOX1, HMOX2, HPGD ALDH1A1 515/4885AURKA 2859/4885DAPK3 1574/4885
US-20160115148-A1 N-SUBSTITUTED HYDROXYLAMINE DERIVATIVES WITH CARBON-BASED LEAVING GROUPS NOS2, NOS3, HMOX2 ALDH1A1 453/4885AURKA 3957/4885DAPK3 1659/4885
US-20140275134-A1 MELDRUM'S ACID, BARBITURIC ACID AND PYRAZOLONE DERIVATIVES SUBSTITUTED WITH HYDROXYLAMINE AS HNO DONORS HMOX1, HMOX2, HPGD ALDH1A1 515/4885AURKA 2859/4885DAPK3 1574/4885

“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.