THIOTEPA

Thiotepa is an alkylating agent used in bonemarrow conditioning and solid tumors. Side effects include profound myelosuppression, mucositis, neurotoxicity, and alopecia. Only GMP materials will be supplied, logistics all according to GDP.

SKU: 9379525dba72 Category: Tag:

Product Description


Mechanism of Action

THIOTEPA exerts multiaxis biochemical modulation involving enzymaticcascade interference, receptormediated signalling adjustment, oxidativestress balancing, mitochondrialrespiratory modulation, ionchannel behaviour influence, cytoskeletalarchitecture modification and transcriptionfactor regulatory alignment. Its molecular topology supports potential interaction with catalytic residues, allosteric microdomains, membraneanchored receptor systems and intracellular signalling scaffolds. These interactions affect phosphorylation circuits, Ca²⁺ signalling, IP/DAG turnover, cAMP regulation, ATP flux and cellular redoxstate stability.

Benefits & Applications

  • Receptorligand interaction and docking studies
  • Kinase/catalytic pathway profiling
  • Mitochondrial ATP/ROS functional modelling
  • Multiomics integration research
  • Cytoskeletal and membranedynamics analysis
  • Apoptosis, autophagy and survivalpathway investigations
  • SAR/QSAR modelling and molecular optimisation

Risks & Side Effects

  • ROS accumulation and oxidativestress imbalance
  • Mitochondrial overload or ETC suppression
  • Ionchannel destabilisation (Ca²⁺/Na⁺/K⁺)
  • Cytoskeletal disruption and membrane integrity loss
  • Dosedependent cytotoxicity
  • Inflammatory cascade activation

Only GMP materials will be supplied, logistics all according to GDP.

Datasheet


Molecular Formula

C6H12N3PS

Molecular Weight

189.22 g/mol

CAS Number

52-24-4

Storage Condition

Keep container tightly closed in a dry and well-ventilated place. Recommended storage temperature 2 – 8 °C.

Solubility

19 g/100 mL at 77 °F (NTP, 1992)

Purity

Purity information is available upon request (COA).

Synonym

thiotepa; 52-24-4; THIO-TEPA; Triethylenethiophosphoramide; Thiophosphamide

IUPAC/Chemical Name

tris(aziridin-1-yl)-sulfanylidene-lambda5-phosphane

InChl Key

FOCVUCIESVLUNU-UHFFFAOYSA-N

InChl Code

InChI=1S/C6H12N3PS/c11-10(7-1-2-7,8-3-4-8)9-5-6-9/h1-6H2

References

https://pubchem.ncbi.nlm.nih.gov/compound/5453;

3D Conformer.

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