Potent inhibitor of platelet aggregation
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13,14-dihydro Prostaglandin E1

Item No. 13610

Technical Information
Formal Name
9-oxo-11α,15S-dihydroxy-prostan-1-oic acid
CAS Number
19313-28-1
Synonyms
  • PGE0
  • 13,14-dihydro PGE1
Molecular Formula
C20H36O5
Formula Weight
Purity
≥98%
A 5 mg/ml solution in methyl acetate
DMF: >100 mg/mlDMSO: >50 mg/mlEthanol: >50 mg/mlPBS (pH 7.2): >1.6 mg/ml
SMILES
O=C1[C@H](CCCCCCC(OC)=O)[C@@H](CC[C@@H](O)CCCCC)[C@H](O)C1
InChi Code
InChI=1S/C21H38O5/c1-3-4-7-10-16(22)13-14-18-17(19(23)15-20(18)24)11-8-5-6-9-12-21(25)26-2/h16-18,20,22,24H,3-15H2,1-2H3/t16-,17+,18+,20+/m0/s1
InChi Key
WWCDWHSPGWIYEH-JRBPQWBISA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
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    Product Description

    13,14-dihydro Prostaglandin E1 (13,14-dihydro PGE1) is a biologically active metabolite of PGE1 with comparable potency to the parent compound.1,2 It is an inhibitor of ADP-induced platelet aggregation in human PRP and washed platelets with IC50 values of 31 and 21 nM, respectively.3 13,14-dihydro PGE1 is a slightly more potent inhibitor of ADP-induced human platelet aggregation than PGE1 (Item No. 13010) which has an IC50 value of 40 nM.4 Also, 13,14-dihydro PGE1 was shown to activate adenylate cyclase in NCB-20 hybrid cells with a Kact value of 668 nM.5

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Änggård, E. The biological activities of three metabolites of prostaglandin E1. Acta Physiol. Scand. 66(4), 509-510 (1966).

    2. Hamberg, M., and Samuelsson, B. On the metabolism of prostaglandins E1 and E2 in man. The Journal of Biological Chemisty 246(22), 6713-6721 (1971).

    3. Kobzar, G., Mardla, V., Järving, I., et alComparison of the inhibitory effect of E-prostaglandins in human and rabbit platelet-rich plasma and washed platelets. Comp. Biochem. Physiol. 106(2), 489-494 (1993).

    4. Kobzar, G., Mardla, V., Järving, I., et alAntiaggregating potency of E-type prostaglandins in human and rabbit platelets. Proc. Estonian Acad. Sci. Chem. 40(N3), 179-180 (1991).

    5. Blair, I.A., Hensby, C.N., and MacDermot, J. Prostacyclin-dependent activation of adenylate cyclase in a neuronal somatic cell hybrid: Prostanoid structure-activity relationships. Br. J. Pharmac. 69(3), 519-525 (1980).