Amsacrine

Amsacrine

SCHEMBL4047

COc1cc(NS(C)(=O)=O)ccc1Nc1c2ccccc2nc2ccccc12

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

TOP2ATOP2B

The experimentally established mechanism targets of Amsacrine. 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
TOP2B known ✓ Q02880 5/20 1.00
TOP2A known ✓ P11388 4/20 1.00
KDM1A O60341 3/20 1.00
CYP1A2 P05177 3/20 1.00
CYP2D6 P10635 3/20 1.00
CYP2C9 P11712 3/20 1.00
GLA P06280 2/20 1.00
CASP1 P29466 2/20 1.00
CASP7 P55210 2/20 1.00
TP53 P04637 2/20 1.00
CYP3A4 P08684 2/20 1.00
TSHR P16473 2/20 1.00
SLC22A1 O15245 1/20 1.00
ABCC4 O15439 1/20 1.00
NR1I2 O75469 1/20 1.00
CHRM1 P11229 1/20 1.00
TOP1 P11387 1/20 1.00
DRD2 P14416 1/20 1.00
ADRA2B P18089 1/20 1.00
ADRA2C P18825 1/20 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
Amsacrine SCHEMBL29360354 1.00 TOP2B (1.00) TOP2BTOP2AKDM1ACYP1A2CYP2D6
Amsacrine SCHEMBL29350869 1.00 TOP2B (1.00) TOP2BTOP2AKDM1ACYP1A2CYP2D6
Amsacrine SCHEMBL28336991 1.00 TOP2B (1.00) TOP2BTOP2AKDM1ACYP1A2CYP2D6
Amsacrine SCHEMBL6256280 1.00 TOP2B (1.00) TOP2BTOP2AKDM1ACYP1A2CYP2D6
Amsacrine SCHEMBL31316257 0.99 KMT2A (1.00) TOP2BTOP2AKDM1ACYP1A2CYP2D6
Amsacrine SCHEMBL1320825 0.99 KMT2A (1.00) TOP2BTOP2AKDM1ACYP1A2CYP2D6
Amsacrine SCHEMBL31237896 0.98 TOP2B (0.95) TOP2BTOP2AKDM1ACYP1A2CYP2D6
Amsacrine SCHEMBL2920983 0.98 TOP2B (0.95) TOP2BTOP2AKDM1ACYP1A2CYP2D6
Amsacrine SCHEMBL21827756 0.94 TOP2B (0.89) TOP2BTOP2AKDM1ACYP1A2CYP2D6
SCHEMBL9739742 0.94 TOP2B (0.88) TOP2BTOP2AKDM1ACYP1A2CYP2D6

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 84173 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
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
CN-122075497-A Use of NLRP3 agonist for tumor treatment 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-20260137806-A1 INTERCALATING SUGAR MOLECULES XALUD THERAPEUTICS, INC. (US) 2026-05-21 US claimed
US-20260137794-A1 LIGAND-DRUG CONJUGATE AND USE THEREOF SYSTIMMUNE INC (US) 2026-05-21 US claimed
EP-4743490-A1 HUMANIZED ANTI-CD7 ANTIBODY Christian-Albrechts-Universität zu Kiel (DE) 2026-05-20 EP claimed
WO-2026099502-A1 NOVEL DRUG CONJUGATES FOR TESTING CELLULAR DRUG UPTAKE Deutsches Krebsforschungszentrum Stiftung des öffentlichen Rechts (DE) 2026-05-15 WO claimed
WO-2026102332-A1 NERVE AND TUMOR HOMING AGENTS AND METHODS OF USE THEREOF Blaze Bioscience, Inc. (US) 2026-05-15 WO claimed
WO-2025136820-A9 POLY-ANTIGEN CYTOKINE-RECEPTOR COMPLEXES (PACCS), COMPOSITIONS, AND METHODS OF USE REGENTS OF THE UNIVERSITY OF MINNESOTA (US) 2026-05-15 WO claimed
EP-0393575-A1 Neoplasia treatment compositions containing antineoplastic agent and side-effect reducing protective agent G.D. Searle & Co. (US) 1990-10-24 EP claimed
EP-0359347-A2 Covalently-linked complexes and methods for enhanced cytotoxicity and imaging NEORX CORPORATION (US) 1990-03-21 EP claimed
EP-0335545-A2 Pharmaceutical formulations for parenteral use UNIVERSITY OF FLORIDA (US) 1989-10-04 EP claimed
US-4704397-A ANTITUMOR AGENTS WARNER-LAMBERT COMPANY (US) 1987-11-03 US claimed
EP-0042553-B1 ANTITUMOR COMPOSITIONS Bristol-Myers Company (US) 1985-09-18 EP claimed
EP-0120907-A1 PHARMACEUTICAL PREPARATIONS FOR USE IN ANTITUMOUR THERAPY Aston Molecules Limited (GB) 1984-10-10 EP claimed
US-4472582-A 3,5-Disubstituted-4'-(9-acridinylamino)-methane-sulfon-m-anisidide compounds having antitumor properties DEVELOPMENT FINANCE CORPORATION OF NEW ZEALAND (NZ) 1984-09-18 US claimed
EP-0035862-B1 PHARMACEUTICALLY ACCEPTABLE SALTS OF 4'-(9-ACRIDINYLAMINO) METHANESULFON-M-ANISIDIDE, THEIR PRODUCTION, AND PHARMACEUTICAL COMPOSITIONS CONTAINING SUCH SALTS WARNER-LAMBERT COMPANY (US) 1984-06-13 EP claimed
WO-1984001506-A1 PHARMACEUTICAL PREPARATIONS FOR USE IN ANTITUMOUR THERAPY UNIV BIRMINGHAM (GB) 1984-04-26 WO claimed
EP-0035862-A2 Pharmaceutically acceptable salts of 4'-(9-acridinylamino) methanesulfon-m-anisidide, their production, and pharmaceutical compositions containing such salts WARNER-LAMBERT COMPANY (US) 1981-09-16 EP claimed