Teniposide

Teniposide

SCHEMBL3908

COc1cc([C@@H]2c3cc4c(cc3[C@@H](O[C@@H]3O[C@@H]5CO[C@@H](c6cccs6)O[C@H]5[C@H](O)[C@H]3O)[C@H]3COC(=O)[C@H]23)OCO4)cc(OC)c1O

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 Teniposide. 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 5/20 1.00
TOP2B known ✓ Q02880 4/20 1.00
CYP3A4 P08684 6/20 1.00
GAA P10253 5/20 1.00
SMN1; SMN2 Q16637 5/20 1.00
NCOA3 Q9Y6Q9 2/20 1.00
ATM Q13315 1/20 1.00
USP2 O75604 1/20 1.00
ABCC3 O15438 1/20 1.00
ABCC4 O15439 1/20 1.00
LMNA P02545 3/20 0.75
MEN1 O00255 2/20 0.75
KMT2A Q03164 2/20 0.75
HSD17B10 Q99714 2/20 0.75
HIF1A Q16665 2/20 0.75
CYP1A2 P05177 1/20 0.75
CYP2D6 P10635 1/20 0.75
CYP2C9 P11712 1/20 0.75
CYP2C19 P33261 1/20 0.75
NCOA1 Q15788 1/20 0.75

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
Teniposide SCHEMBL6027493 1.00 CYP3A4 (1.00) CYP3A4GAASMN1; SMN2TOP2ATOP2B
Teniposide SCHEMBL14008692 1.00 CYP3A4 (1.00) CYP3A4GAASMN1; SMN2TOP2ATOP2B
Teniposide SCHEMBL9607866 1.00 CYP3A4 (1.00) CYP3A4GAASMN1; SMN2TOP2ATOP2B
Teniposide SCHEMBL5968656 1.00 CYP3A4 (1.00) CYP3A4GAASMN1; SMN2TOP2ATOP2B
Teniposide SCHEMBL94844 1.00 CYP3A4 (1.00) CYP3A4GAASMN1; SMN2TOP2ATOP2B
Teniposide SCHEMBL14031677 1.00 CYP3A4 (1.00) CYP3A4GAASMN1; SMN2TOP2ATOP2B
Teniposide SCHEMBL23202938 1.00 CYP3A4 (1.00) CYP3A4GAASMN1; SMN2TOP2ATOP2B
Teniposide SCHEMBL12278906 1.00 CYP3A4 (1.00) CYP3A4GAASMN1; SMN2TOP2ATOP2B
Teniposide SCHEMBL13809319 1.00 CYP3A4 (1.00) CYP3A4GAASMN1; SMN2TOP2ATOP2B
Teniposide SCHEMBL13712547 1.00 CYP3A4 (1.00) CYP3A4GAASMN1; SMN2TOP2ATOP2B

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 145009 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-4747263-A1 LIPID NANOPARTICLES AND USES THEREOF University of Connecticut (US) 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
WO-2026103267-A1 USE OF SESQUITERPENOIDS IN RELIEVING NAUSEA AND VOMITING 辽宁新中现代医药有限公司 2026-05-21 WO claimed
WO-2026104998-A1 SUBSTITUTED IMIDAZOPYRIDINE COMPOUND DERIVATIVES AND THEIR PHARMACEUTICAL USE AVELOS THERAPEUTICS INC. (KR) 2026-05-21 WO claimed
WO-2026107377-A1 PHARMACOLOGICAL RE-ACTIVATION OF MUTANT PVHL KARANICOLAS JOHN (US) 2026-05-21 WO claimed
US-20260137794-A1 LIGAND-DRUG CONJUGATE AND USE THEREOF SYSTIMMUNE INC (US) 2026-05-21 US claimed
US-20260137700-A1 PHARMACEUTICAL COMBINATION OF PRMT5 INHIBITOR AND DNA DAMAGE-INDUCING SUBSTANCE SK BIOPHARMACEUTICALS CO LTD (KR) 2026-05-21 US claimed
WO-2026105121-A1 ANTICANCER FORMULATIONS AND USES THEREOF INTRAGEL THERAPEUTICS LTD. (IL) 2026-05-21 WO claimed
EP-0302473-A2 Antibody-enzyme conjugates in combination with prodrugs for the delivery of cytotoxic agents to tumor cells Bristol-Myers Squibb Company (US) 1989-02-08 EP claimed
US-4766149-A SYNERGISTIC MIXTURE WITH ANTITUMOR AND ANTICARCINOGENIC AGENTS STIFTUNG DEUTSCHES KREBSFORSCHUNGSZENTRUM (DE) 1988-08-23 US claimed
WO-1988003799-A1 PHARMACEUTICAL VEHICLES FOR REDUCING TRANSDERMAL FLUX CHEMEX PHARMACEUTICALS, INC. (US) 1988-06-02 WO claimed
EP-0221176-A4 PHARMACEUTICAL VEHICLES FOR RECUCING TRANSDERMAL FLUX. CHEMEX PHARMACEUTICALS INC (US) 1988-01-25 EP claimed
EP-0226202-A2 Synthesis of podophylotoxin type compounds BAR-ILAN UNIVERSITY (IL) 1987-06-24 EP claimed
EP-0221176-A1 PHARMACEUTICAL VEHICLES FOR RECUCING TRANSDERMAL FLUX. CHEMEX PHARMACEUTICALS INC (US) 1987-05-13 EP claimed
WO-1986006586-A1 PHARMACEUTICAL VEHICLES FOR RECUCING TRANSDERMAL FLUX CHEMEX PHARMACEUTICALS, INC. (US) 1986-11-20 WO claimed
EP-0120907-A1 PHARMACEUTICAL PREPARATIONS FOR USE IN ANTITUMOUR THERAPY Aston Molecules Limited (GB) 1984-10-10 EP claimed
WO-1984001506-A1 PHARMACEUTICAL PREPARATIONS FOR USE IN ANTITUMOUR THERAPY UNIV BIRMINGHAM (GB) 1984-04-26 WO claimed
EP-0019167-B1 MEDICINAL PREPARATION FOR THE TREATMENT OF CARCINOMA AND PROCESS FOR PREPARING IT Limburg, Hans, Dr. (DE) 1983-10-12 EP claimed