A STAT3 inhibitor
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STA-21

Item No. 14996

Technical Information
Formal Name
(3S)-3,4-dihydro-8-hydroxy-3-methyl-benz[a]anthracene-1,7,12(2H)-trione
CAS Number
28882-53-3
Synonyms
  • Ochromycinone
Molecular Formula
C19H14O4
Formula Weight
Purity
≥95%
Formulation
A crystalline solid
DMF: 25 mg/mlDMF:PBS(pH7.2) (1:2): 0.3 mg/mlDMSO: 16 mg/ml
λmax
265, 400 nm
SMILES
O=C1C2=C(C=CC(C[C@H](C)C3)=C2C3=O)C(C4=C(O)C=CC=C41)=O
InChi Code
InChI=1S/C19H14O4/c1-9-7-10-5-6-12-17(15(10)14(21)8-9)19(23)11-3-2-4-13(20)16(11)18(12)22/h2-6,9,20H,7-8H2,1H3/t9-/m0/s1
InChi Key
ZAWXOCUFQSQDJS-VIFPVBQESA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    STA-21 is a natural antibiotic that potently inhibits STAT3 by preventing its dimerization and DNA binding when used at concentrations of 20-30 μM.1 It blocks the growth and survival of cancer cells that express constitutively active STAT3 (e.g., DU145 cells, IC50 = 12.2 μM).1,2,3 STAT3 inhibitors, including STA-21, prevent the proliferation of human keratinocytes and have value in improving psoriasis.4

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Song, H., Wang, R., Wang, S., et alA low-molecular-weight compound discovered through virtual database screening inhibits Stat3 function in breast cancer cells. Proc. Natl. Acad. Sci. USA 102(13), 4700-4705 (2005).

    2. Bhasin, D., Cisek, K., Pandharkar, T., et alDesign, synthesis, and studies of small molecule STAT3 inhibitors. Bioorg. Med. Chem. Lett. 18(1), 391-395 (2008).

    3. Chen, C.L., Loy, A., Cen, L., et alSignal transducer and activator of transcription 3 is involved in cell growth and survival of human rhabdomyosarcoma and osteosarcoma cells. BMC Cancer 7, 111 (2007).

    4. Miyoshi, K., Takaishi, M., Nakajima, K., et alStat3 as a therapeutic target for the treatment of psoriasis: A clinical feasibility study with STA-21, a Stat3 inhibitor. J. Invest. Dermatol. 131(1), 108-117 (2011).