Chemodex

Triptolide

CHF 102.00
In stock
CDX-T0237-M0011 mgCHF 102.00
CDX-T0237-M0055 mgCHF 380.00
More Information
Product Details
Synonyms PG 490; NSC163062; TPL
Product Type Chemical
Properties
Formula

C20H24O6

MW 360.40
CAS 38748-32-2
Purity Chemicals ≥98% (HPLC)
Appearance White to off-white powder.
Solubility Soluble in DMSO.
Identity Determined by 1H-NMR.
Declaration Manufactured by Chemodex.
Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key DFBIRQPKNDILPW-KTGKZQHOSA-N
Smiles O=C(OC1)C2=C1C(C[C@H](O3)[C@]43[C@@]56[C@@H](O6)[C@H]7[C@@](O7)(C(C)C)[C@H]4O)[C@]5(C)CC2
Shipping and Handling
Shipping AMBIENT
Short Term Storage +4°C
Long Term Storage +4°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at +4°C.
Documents
MSDS Inquire
Product Specification Sheet
Datasheet Download PDF
Description

Potent immunosuppressant with anti-inflammatory and antitumor properties. Exhibits potent antiproliferative activity, induces apoptosis, modulates autophagy and inhibits cell cycle regulators. Inhibits global gene transcription by inducing degradation of RNA polymerase II (Pol II) and by inhibiting the ATPase activity of XPB (a subunit of the general transcription factor TFIIH). Interferes with a number of transcription factors including p53, NF-κB, nuclear factor of activated T cells (NFAT) and heat shock factor protein 1 (HSF-1). Shown to inhibit aromatase activity.

Product References

(1) S.M. Kupchan, et al.; JACS 94, 7194 (1972) | (2) Y. Yang, et al.; Immunopharmacology 40, 139 (1998) | (3) H. Liu, et al.; Acta Pharmacol. Sin. 21, 782 (2000) | (4) B.J. Chen; Leuk. Lymphoma 42, 253 (2001) (Review) | (5) S. Yang, et al.; Mol. Cancer Ther. 2, 65 (2003) | (6) S.M. Johnson, et al.; J. Surg. Res. 168, 197 (2011) | (7) J. Pan; Cancer Lett. 292, 149 (2010) (Review) | (8) N. Mujumdar, et al.; Gastroenterol. 139, 598 (2010) | (9) D.V. Titov, et al.; Nat. Chem. Biol. 7, 182 (2011) | (10) J. Zhang, et al.; Arzneimittelforschung 61, 727 (2011) | (11) Y. Lu, et al.; Chem. Biol. 21, 246 (2014)

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