Mitoxantrone

Mitoxantrone

SCHEMBL3000

O=C1c2c(O)ccc(O)c2C(=O)c2c(NCCNCCO)ccc(NCCNCCO)c21

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

TOP2A

The experimentally established mechanism targets of Mitoxantrone. 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
TOP2A known ✓ P11388 2/20 1.00
MEN1 O00255 6/20 1.00
KMT2A Q03164 6/20 1.00
MAPK1 P28482 4/20 1.00
TDP1 Q9NUW8 4/20 1.00
LMNA P02545 3/20 1.00
BLM P54132 3/20 1.00
USP2 O75604 3/20 1.00
TP53 P04637 3/20 1.00
RECQL P46063 3/20 1.00
NSD2 O96028 3/20 1.00
NPC1 O15118 3/20 1.00
RAB9A P51151 3/20 1.00
CSNK2A2 P19784 3/20 1.00
CSNK2B P67870 3/20 1.00
CSNK2A1 P68400 3/20 1.00
CSNK2A3 Q8NEV1 3/20 1.00
SMN1; SMN2 Q16637 2/20 1.00
MTOR P42345 2/20 1.00
CYP3A4 P08684 2/20 1.00

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
Mitoxantrone SCHEMBL20214110 1.00 MEN1 (1.00) MEN1KMT2AMAPK1TDP1LMNA
Mitoxantrone SCHEMBL29353270 1.00 MEN1 (1.00) MEN1KMT2AMAPK1TDP1LMNA
SCHEMBL11038495 1.00 MEN1 (1.00) MEN1KMT2AMAPK1TDP1LMNA
SCHEMBL11036806 1.00 MEN1 (1.00) MEN1KMT2AMAPK1TDP1LMNA
SCHEMBL11517949 1.00 MEN1 (1.00) MEN1KMT2AMAPK1TDP1LMNA
SCHEMBL11391594 1.00 MEN1 (1.00) MEN1KMT2AMAPK1TDP1LMNA
Mitoxantrone SCHEMBL29720597 1.00 MEN1 (1.00) MEN1KMT2AMAPK1TDP1LMNA
SCHEMBL11041207 1.00 MEN1 (1.00) MEN1KMT2AMAPK1TDP1LMNA
Mitoxantrone SCHEMBL2342900 0.98 MEN1 (1.00) MEN1KMT2AMAPK1TDP1LMNA
Hydrochloric Acid SCHEMBL10522176 0.98 MEN1 (1.00) MEN1KMT2AMAPK1TDP1LMNA

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

Appears in 181702 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4749286-A2 METHOD OF ASSESSING RISK OF PML Biogen MA Inc. (US) 2026-05-27 EP claimed
EP-4748859-A2 CHEMICALLY AND PHOTOCHEMICALLY INITIATED CELL MEMBRANE BLEBBING TO INDUCE CELL VESICLE PRODUCTION, MODIFICATIONS THEREOF, AND USES THEREOF The Regents of the University of California (US) 2026-05-27 EP claimed
EP-3607938-B1 PHARMACEUTICAL COMPOSITION SOVIC BRKICIC LJILJANA (HR) 2026-05-27 EP claimed
EP-4747263-A1 LIPID NANOPARTICLES AND USES THEREOF University of Connecticut (US) 2026-05-27 EP claimed
CN-224285143-U Dihydroxyanthraquinone is with high-efficient dewatering device Inner Mongolia Baohong Chemical Technology Co.,Ltd. (CN) 2026-05-26 CN claimed
CN-116209439-B Cereblon protein modulators Saint Jude Children's Research Hospital Ltd. (US) 2026-05-26 CN claimed
US-20260137671-A1 PDK4 as a Cell-Aging Intervention Target and Its Use in Chemotherapy and Anticancer SHANGHAI INST OF NUTRITION AND HEALTH CHINESE ACADEMY OF SCIENCES (CN) 2026-05-21 US claimed
US-20260137680-A1 NOVEL COMPOUNDS SITRYX THERAPEUTICS LTD (GB) 2026-05-21 US claimed
WO-2026102563-A1 DISUBSTITUTED PYRIMIDOPYRROLE ANALOG AND USE THEREOF 深圳湾实验室坪山生物医药研发转化中心 2026-05-21 WO claimed
WO-2026105121-A1 ANTICANCER FORMULATIONS AND USES THEREOF INTRAGEL THERAPEUTICS LTD. (IL) 2026-05-21 WO claimed
US-4292248-A BY HEATING THE CORRESPONDING DINITRO COMPOUND WITH SODIUM OR POTASSIUM FORMATE IN DIMETHYLFORMAMIDE AMERICAN COLOR & CHEMICAL CORPORATION (US) 1981-09-29 US claimed
EP-0000341-B1 PROCESS FOR PREPARING PRACTICALLY PURE 1-AMINO-8-NITRO-4,5-DIHYDROXY ANTHRAQUINONE BASF Aktiengesellschaft (DE) 1981-02-25 EP claimed
US-4248721-A MIXTURE OF CARBOXYLIC PENTAERYTHRITOL ESTER, PHENYL NAPHTHYLAMINE, DIPHENYLAMINE, POLYHYDROXYANTHRAQUINONE, PHOSPHATE ESTER, THIADIAZOLE DERIVATIVE TEXACO INC. (US) 1981-02-03 US claimed
US-4188298-A ACYCLIC ESTER, ARYLAMINES, SULFIDES AND ARYL PHOSPHATES, OXIDATIVE STABILITY TEXACO INC. (US) 1980-02-12 US claimed
US-4179386-A ALIPHATIC ESTER OIL, ARYL PHOSPHATE, POLYHYDROXYANTHRAQUINONE, DIALKYL SULFIDE, PHENYLNAPHTHYLAMINE OR DIALKYLDIPHENYLAMINE TEXACO INC. (US) 1979-12-18 US claimed
US-4157970-A ALIPHATIC ESTER, A PHENYL NAPHTHYLAMINE, A PHOSPHATE ESTER, A POLYHYDROXY ANTHRAQUINONE, AND AN ALKYL MERCAPTO ACID ESTER TEXACO INC. (US) 1979-06-12 US claimed
US-4157971-A ALIPHATIC ESTER, PHENYL NAPHTHYLAMINES, PHOSPHATE ESTER, POLYHYDROXY ANTHRAQUINONE, ALKYL THIOACID ESTER TEXACO INC. (US) 1979-06-12 US claimed
US-4119551-A OXIDATION RESISTANCE, NAPHTHYLPHENYLAMINES AND DIPHENYLAMINES, POLYHYDROXYANTHRAQUINONE, PHOSPHATE ESTER, BIS/DIALKYLTHIOCARBAMYL) SULFIDE TEXACO INC. (US) 1978-10-10 US claimed
US-4002654-A Process for the preparation of dihydroxyanthraquinones BAYER AKTIENGESELLSCHAFT (DT) 1977-01-11 US claimed
US-3977953-A PHOTOSENSITIZED OXIDATION OF LUPULONES ATLANTIC RESEARCH INSTITUTE LTD. (BA) 1976-08-31 US claimed