Anthraquinone

Anthraquinone

SCHEMBL10902508

CCO.O=C1c2ccccc2C(=O)c2ccccc21

nearest known ligand 0.67

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

MMP1MMP13MMP7MMP8polrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Anthraquinone. 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
MEN1 O00255 6/20 0.67
KMT2A Q03164 6/20 0.67
CDC25B P30305 6/20 0.67
RAB9A P51151 6/20 0.56
SMN1; SMN2 Q16637 6/20 0.56
MAPT P10636 6/20 0.56
LMNA P02545 5/20 0.56
NPC1 O15118 5/20 0.56
MAPK1 P28482 4/20 0.56
ALDH1A1 P00352 4/20 0.56
L3MBTL1 Q9Y468 2/20 0.56
S100A4 P26447 4/20 0.55
APAF1 O14727 3/20 0.55
TDP2 O95551 3/20 0.55
KDM4E B2RXH2 3/20 0.55
BLM P54132 3/20 0.55
POLB P06746 3/20 0.55
PLA2G1B P04054 2/20 0.55
THRB P10828 2/20 0.55
RECQL P46063 2/20 0.55

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
9,10-Phenanthrenequinone SCHEMBL28567802 0.92 S100A4 (0.68) MEN1KMT2ACDC25BRAB9ASMN1; SMN2
Anthraquinone SCHEMBL616605 0.86 MEN1 (0.71) MEN1KMT2ACDC25BRAB9ASMN1; SMN2
Anthraquinone SCHEMBL11302120 0.85 CDC25B (0.80) MEN1KMT2ACDC25BRAB9ASMN1; SMN2
Anthraquinone SCHEMBL28215858 0.83 CDC25B (0.67) MEN1KMT2ACDC25BRAB9ASMN1; SMN2
Anthraquinone SCHEMBL28758919 0.83 MEN1 (0.67) MEN1KMT2ACDC25BRAB9ASMN1; SMN2
Anthraquinone SCHEMBL430600 0.83 MEN1 (0.67) MEN1KMT2ACDC25BRAB9ASMN1; SMN2
Anthraquinone SCHEMBL7856851 0.82 MEN1 (0.57) MEN1KMT2ACDC25BRAB9ASMN1; SMN2
Anthraquinone SCHEMBL17747127 0.82 CDC25B (0.57) MEN1KMT2ACDC25BRAB9ASMN1; SMN2
Anthraquinone SCHEMBL27767988 0.82 MEN1 (0.57) MEN1KMT2ACDC25BRAB9ASMN1; SMN2
Anthraquinone SCHEMBL5958714 0.82 CDC25B (0.86) MEN1KMT2ACDC25BRAB9ASMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113509751-B Extraction-back extraction system based on alkanol eutectic solvent and application thereof 武汉大学 2022-07-19 CN disclosed
US-11236207-B2 Solid state electrodes and sensors PARKER HANNIFIN CORP (US) 2022-02-01 US disclosed
CN-113509751-A Extraction-back extraction system based on alkanol eutectic solvent and application thereof 武汉大学 2021-10-19 CN disclosed
US-20200207928-A1 SOLID STATE ELECTRODES AND SENSORS PARKER HANNIFIN CORP (US) 2020-07-02 US disclosed
US-10538635-B2 Solid state electrodes and sensors PARKER INTANGIBLES LLC 2020-01-21 US disclosed
EP-3155408-B1 SOLID STATE ELECTRODES AND SENSORS PARKER HANNIFIN CORP (US) 2019-05-22 EP disclosed
CN-106159195-B A kind of battery core and the lithium ion battery comprising the battery core 比亚迪股份有限公司 2018-12-21 CN disclosed
EP-3155408-A1 SOLID STATE ELECTRODES AND SENSORS Parker-Hannifin Corporation (US) 2017-04-19 EP disclosed
US-20170101513-A1 SOLID STATE ELECTRODES AND SENSORS Parker-Hannifin Coporation (US) 2017-04-13 US disclosed
WO-2015191924-A1 SOLID STATE ELECTRODES AND SENSORS SENOVA SYSTEMS, INC. (US) 2015-12-17 WO disclosed
CN-103374246-A Flexible uv-curable coating compositions SDC TECHNOLOGIES INC 2013-10-30 CN disclosed
US-4597830-A FREE OF SODIUM HYDROXIDE AND SULFIDES THE UNIVERSITY OF ALABAMA (US) 1986-07-01 US disclosed