Anthraquinone

Anthraquinone

SCHEMBL21646088

C1=CC=CNC=C1.O=C1c2ccccc2C(=O)c2ccccc21

nearest known ligand 0.60

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Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ MEN1 O00255 2/20 0.60
▸ KMT2A Q03164 2/20 0.60
▸ CDC25B P30305 2/20 0.60
▸ RAB9A P51151 4/20 0.50
▸ POLB P06746 3/20 0.50
▸ APAF1 O14727 3/20 0.50
▸ SMN1; SMN2 Q16637 3/20 0.50
▸ MAOA P21397 3/20 0.50
▸ KDM4E B2RXH2 2/20 0.50
▸ LMNA P02545 2/20 0.50
▸ MAPT P10636 2/20 0.50
▸ BLM P54132 2/20 0.50
▸ TDP2 O95551 2/20 0.50
▸ NPC1 O15118 2/20 0.50
▸ MAPK1 P28482 2/20 0.50
▸ S100A4 P26447 2/20 0.50
▸ CES2 O00748 1/20 0.50
▸ TERT O14746 1/20 0.50
▸ PLIN1 O60240 1/20 0.50
▸ S1PR4 O95977 1/20 0.50

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
Anthraquinone SCHEMBL28270692 1.00 MEN1 (0.60) MEN1KMT2ACDC25BRAB9APOLB
SCHEMBL28245677 0.98 MEN1 (0.57) MEN1KMT2ACDC25BRAB9APOLB
SCHEMBL28272504 0.84 MEN1 (0.38) MEN1KMT2ACDC25BRAB9APOLB
Anthrone SCHEMBL27433230 0.83 MAOA (0.69) MEN1KMT2ACDC25BRAB9ASMN1; SMN2
Phthalimide SCHEMBL27471434 0.81 GSK3B (0.68) MEN1KMT2ACDC25BPOLBSMN1; SMN2
Naphthoquinone SCHEMBL27950218 0.81 CDC25B (0.64) MEN1KMT2ACDC25BRAB9APOLB
Anthraquinone SCHEMBL2478622 0.78 MEN1 (0.86) MEN1KMT2ACDC25BRAB9APOLB
Anthraquinone SCHEMBL1445042 0.78 MEN1 (0.86) MEN1KMT2ACDC25BRAB9APOLB
Anthraquinone SCHEMBL29358690 0.78 MEN1 (1.00) MEN1KMT2ACDC25BRAB9APOLB
Anthraquinone SCHEMBL14943 0.78 MEN1 (1.00) MEN1KMT2ACDC25BRAB9APOLB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-101712648-B Synthesis method of azepine anthraquinone NANJING UNIVERSITY OF TECHNOLOGY 2011-11-09 — — CN claimed
CN-101712648-A Synthesis method of azepine anthraquinone NANJING UNIVERSITY OF TECHNOLOGY 2010-05-26 — — CN claimed
US-20240041849-A1 COMPOUNDS FOR THE TREATMENT OF NEUROLOGICAL OR MITOCHONDRIAL DISEASES MUSC FOUNDATION FOR RESEARCH DEVELOPMENT (US) 2024-02-08 — — US disclosed
US-11771685-B2 Compounds for the treatment of neurological or mitochondrial diseases MUSC FOUNDATION FOR RESEARCH DEVELOPMENT (US) 2023-10-03 — — US disclosed
US-20220125774-A1 COMPOUNDS FOR THE TREATMENT OF NEUROLOGICAL OR MITOCHONDRIAL DISEASES MUSC FOUNDATION FOR RESEARCH DEVELOPMENT (US) 2022-04-28 — — US disclosed
EP-3829560-A1 COMPOUNDS FOR THE TREATMENT OF NEUROLOGICAL OR MITOCHONDRIAL DISEASES Musc Foundation for Research Development (US) 2021-06-09 — — EP disclosed
WO-2020028222-A1 COMPOUNDS FOR THE TREATMENT OF NEUROLOGICAL OR MITOCHONDRIAL DISEASES MUSC FOUNDATION FOR RESEARCH DEVELOPMENT (US) 2020-02-06 — — WO disclosed
CN-105637038-B Novel compound and composition containing the same 株式会社艾迪科 2019-10-25 — — CN disclosed
CN-104334684-B Latent additive and composition containing the same 株式会社艾迪科 2019-08-27 — — CN disclosed
CN-109922793-A Poorly water soluble dietary supplements and methods of solubilizing pharmaceutically active agents 雅典娜股份公司 2019-06-21 — — CN disclosed
CN-108699183-A Composition and new compound 株式会社艾迪科 2018-10-23 — — CN disclosed
CN-104334684-A Latent additive and composition containing the same ADEKA CORP 2015-02-04 — — CN disclosed
CN-101712648-B Synthesis method of azepine anthraquinone NANJING UNIVERSITY OF TECHNOLOGY 2011-11-09 — — CN disclosed
CN-101712648-B Synthesis method of azepine anthraquinone NANJING UNIVERSITY OF TECHNOLOGY 2011-11-09 — — CN disclosed
CN-101712648-B Synthesis method of azepine anthraquinone NANJING UNIVERSITY OF TECHNOLOGY 2011-11-09 — — CN disclosed
CN-101712648-A Synthesis method of azepine anthraquinone NANJING UNIVERSITY OF TECHNOLOGY 2010-05-26 — — CN disclosed
CN-101712648-A Synthesis method of azepine anthraquinone NANJING UNIVERSITY OF TECHNOLOGY 2010-05-26 — — CN disclosed
CN-101712648-A Synthesis method of azepine anthraquinone NANJING UNIVERSITY OF TECHNOLOGY 2010-05-26 — — CN disclosed
CN-1139575-C Process for preparing quinoline-5, 8-diones L���������鹫˾ 2004-02-25 — — CN disclosed
CN-1370149-A Process for preparing quinoline-5, 8-diones LAFON LABOR (FR) 2002-09-18 — — CN 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-20240041849-A1 COMPOUNDS FOR THE TREATMENT OF NEUROLOGICAL OR MITOCHONDRIAL DISEASES MT-ND2, MT-ND1, NLN MEN1 917/4885KMT2A 869/4885CDC25B 3047/4885
US-11771685-B2 Compounds for the treatment of neurological or mitochondrial diseases MT-ND2, MT-ND1, NLN MEN1 917/4885KMT2A 869/4885CDC25B 3047/4885
US-20220125774-A1 COMPOUNDS FOR THE TREATMENT OF NEUROLOGICAL OR MITOCHONDRIAL DISEASES MT-ND2, MT-ND1, NLN MEN1 917/4885KMT2A 869/4885CDC25B 3047/4885

“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.

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