A derivative of biopterin
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Information provided in the product description is from published literature. Due to the nature of scientific experimentation, your results (e.g., selectivity and effective concentrations) or specific application for this product may differ. If you have questions about how this product fits your application, please contact our technical support staff.

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Rhamnopterin

Item No. 35254

Technical Information
Formal Name
2-amino-6-(1,2,3-trihydroxybutyl)-4(3H)-pteridinone
CAS Number
13392-24-0
Molecular Formula
C10H13N5O4
Formula Weight
Purity
≥95%
A solid
SMILES
O=C1N=C(N)N=C2NC=C(C(C(C(C)O)O)O)N=C12
InChi Code
InChI=1S/C10H13N5O4/c1-3(16)6(17)7(18)4-2-12-8-5(13-4)9(19)15-10(11)14-8/h2-3,6-7,16-18H,1H3,(H3,11,12,14,15,19)
InChi Key
QSVZLFABRHDXRR-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Rhamnopterin is a derivative of L-biopterin (Item No. 10007662), the oxidized form of tetrahydro-L-biopterin (BH4), and D-biopterin (Item No. 34201).1 Dietary administration of rhamnopterin (0.5%) concurrently with the carcinogen 4-dimethylaminoazobenzene reduces the incidence of 4-dimethylaminoazobenzene-induced liver tumors in rats. Rhamnopterin has been used as an internal standard for the quantification of biopterin and neopterin in rat plasma by LC-MS.2

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Sasaki, H., Nagase, S., Fujimaki, C., et alEffect of polyhydroxy-alkylpterins on the development of liver cancers in the rat fed with 4-dimethylaminoazobenzene. Gan. 55, 297-304 (1964).

    2. Pickert, G., Lim, H.-Y., Weigert, A., et alInhibition of GTP cyclohydrolase attenuates tumor growth by reducing angiogenesis and M2-like polarization of tumor associated macrophages. Int. J. Cancer 132(3), 591-604 (2013).