Actinomycin D

SKU:BHB11900067
Suppliers
StressMarq Biosciences Inc.
StressMarq Biosciences Inc.
Details Products
Overview
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Actinomycin D is a research-grade small-molecule inhibitor of Transcription for Cancer and Apoptosis studies. Supplied as a red-orange powder with >98% purity (CAS 50-76-0, MW 1255.43) Soluble to 50 mM in DMSO; store at -20°C. For research use only.
Cas No. 50-76-0
Molecular Formula C62H86N12O16
Purity >98%
Application Notes Transcription inhibitor
Options selector
Catalog no. Size
SIH-245-10MG 10 mg
SIH-245-50MG 50 mg
Available Options

Select the variant that best fits your experiment. Availability and lead time may vary by option.

  • Options: Size (2) — 10 mg, 50 mg.
  • Lead time: options listed as “in stock at manufacturer” typically ship in 2-3 business days; other statuses may take longer.
  • Storage: -20ºC
  • Shipping: ships at ambient temperature.
  • Upon receipt: store at the recommended temperature as soon as possible.
  • Sales terms and conditions: Please review prior to ordering.
Field Specification
Alternative names 2-Amino-N,N'-bis(6,13-diisopropyl-2,5,9-trimethyl-1,4,7,11,14-pentaoxohexadecahydro-1H-pyrrolo[2,1-i][1,4,7,10,13]oxatetraazacyclohexadecin-10-yl)-4,6-dimethyl-3-oxo-3H-phenoxazine-1,9-dicarboxamide
CAS no. 50-76-0
Applications
  • Functional Assay (In Vitro)
Source Synthetic
Molecular weight 1255.43
Molecular formula C62H86N12O16
Purity >98%
Bioactivity Inhibitor
Activity
  • Inhibitor
Solubility Soluble to 50 mM in DMSO
SMILES CC1C(C(=O)NC(C(=O)N2CCCC2C(=O)N(CC(=O)N(C(C(=O)O1)C(C)C)C)C)C(C)C)NC(=O)C3=C4C(=C(C=C3)C)OC5=C(C(=O)C(=C(C5=N4)C(=O)NC6C(OC(=O)C(N(C(=O)CN(C(=O)C7CCCN7C(=O)C(NC6=O)C(C)C)C)C)C(C)C)C)N)C
InChIKey RJURFGZVJUQBHK-UHFFFAOYSA-N
Form Red-orange powder
Storage -20ºC
Shipping Shipped Ambient
Catalog no. (Mfr.) SIH-245
Main SKU BHB11900067

Actinomycin D is a polypeptide antibiotic that inhibits transcription by binding to DNA and preventing RNA polymerase elongation. In neuroscience, it is used to study gene expression regulation, transcriptional responses to stress, and the role of RNA synthesis in neuronal survival and plasticity.

Classification: Very Toxic. May be fatal if inhaled, swallowed or absorbed through skin.

Safety Phrases:

  • S22 - Do not breathe dust
  • S24/25 - Avoid contact with skin and eyes
  • S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection
  • S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label where possible)

Risk Phrases:

  • R26/27/28 - Very Toxic by inhalation, in contact with skin and if swallowed
  • R36/37/38 - Irritating to eyes, respiratory system and skin
  • R40 - Limited evidence of a carcinogenic effect
  • R62 - Possible risk of impaired fertility

Hazard Phrases:

H300 – Fatal if swallowed

Precautionary Phrases:

P264 –P301 + P310

Actinomycin D (StressMarq Biosciences Inc., Victoria BC CANADA, Catalog # SIH-245)

Need this compound in a format that drops straight into your assay? We can tailor formulation, chemistry, and documentation so your results stay consistent across runs and re-orders.

  • Format options: solid or pre-dissolved solution (choose solvent), target concentration, aliquots, light/moisture-protected packaging
  • Chemistry options: free base/acid vs salt forms, hydrate/solvate preference, stereoisomer control (single enantiomer or racemate), close analogs
  • Add-on labels & handles: D/¹³C/¹⁵N isotopes (LC-MS/internal standards), azide/alkyne or other functional handles for conjugation
  • QC & documentation: standard COA or enhanced analytical pack (HPLC/LC-MS/NMR), chiral purity, residual solvents, water content (KF), method-specific specs
  • Scale & continuity: mg to gram scale, bulk pricing, lot reservation, repeat-order continuity

To quote quickly, tell us: compound name + CAS/structure (SMILES or mol file), intended assay context, solvent preference, salt/stereochemistry requirements, purity/QC level, and the amount (mg–g).

Can’t find the compound you’re looking for?
Send the CAS or structure and your specs. We can help source it, suggest close equivalents, or discuss custom synthesis with the right QC documentation (RUO).

1. Sobell H. (1985) Proc Natl Acad Sci USA. 82(16): 5328-31.
2. Turan T., et al. (2006) Int J Gynecol Cancer. 16(3): 1432-1438.
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