An active metabolite of pregnenolone
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16-Dehydroprogesterone

Item No. 43057

Technical Information
Formal Name
pregna-4,16-diene-3,20-dione
CAS Number
1096-38-4
Synonyms
  • NSC 9785
  • NSC 11037
  • Δ16-Progesterone
Molecular Formula
C21H28O2
Formula Weight
Purity
≥98%
A solid
DMSO: Sparingly soluble: 1-10 mg/mlEthanol: Sparingly soluble: 1-10 mg/ml
SMILES
C[C@@]12[C@]3([H])[C@](CCC1=CC(CC2)=O)([H])[C@@]4([H])[C@](CC3)(C(C(C)=O)=CC4)C
InChi Code
InChI=1S/C21H28O2/c1-13(22)17-6-7-18-16-5-4-14-12-15(23)8-10-20(14,2)19(16)9-11-21(17,18)3/h6,12,16,18-19H,4-5,7-11H2,1-3H3/t16-,18-,19-,20-,21+/m0/s1
InChi Key
VRRHHTISESGZFN-RKFFNLMFSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
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    Product Description

    16-Dehydroprogesterone is a progestin and an active metabolite of pregnenolone (Item No. 19864).1,2,3 It inhibits the proliferation of HL-60 leukemia and U937 lymphoma cells (IC50s = 10.9 and 3.6 µM, respectively).2 16-Dehydroprogesterone (2 mg/kg), in combination with gonadotropin, increases ovary and uterine weights in prepuberal rhesus monkeys.3

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Kwan, T.K., Taylor, N.F., and Gower, D.B. The use of steroid profiling in the resolution of pregnenolone metabolites from porcine testicular preparations. J. Chromatogr. 301(1), 189-197 (1984).

    2. Samudio, I., Konopleva, M., Safe, S., et alGuggulsterones induce apoptosis and differentiation in acute myeloid leukemia: identification of isomer-specific antileukemic activities of the pregnadienedione structure. Mol. Cancer Ther. 4(12), 1982-1992 (2005).

    3. Kar, A.B., and Chandra, H. Effect of some progestational steroids on the response of the ovary of prepuberal rhesus monkeys to exogenous gonadotrophin. Steroids 6(4), 463-472 (1965).