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    Default phenomenally pheromonal molecular hybrid hypothesis

    PREFACE: Hello, I'm the archetypical hybrid

    (HEC)

    I'm a student majoring in neuropharmacology, organic chemistry, chemical &

    mechanical engineering, and I'm conducting some private research on phenomenal pheromones as described

    hereafter.


    For your referances:
    androsta-4,16-dien-3-one =

    androstadienone
    5α-androstan-3-one =

    androstAnone

    5α-androst-16-en-3-one = androstenone
    4-androsten-3-one

    = 4-androstenone

    Based upon the quantitative structure-property relationships I've studied for

    steroids which are active at the human female VNO, I believe that 4-ANDROSTEN-3-ONE (DESOXYTESTOSTERONE), may be

    very active at the human female VNO. This hypothesis is derived from the fact that only two pheromones:

    androsta-4,16-dien-3-one, and 5α-androstan-3-one are significantly active at the human female

    VNO [as substantiated by an Erox study long ago titled: the sixth sense].

    5α-androstan-3-one is a saturated analogue of 5α-androst-16-en-3-one (a pig

    pheromone), which has an alkene group at the 16th carbon of the prototypical skeletal molecule.



    5α-androst-16-en-3-one does not target the human female VNO, whereas

    5α-androstan-3-one does; the only difference being the alkene group at the 16th carbon. Now,

    androsta-4,16-dien-3-one, an analogue of 5α-androst-16-en-3-one is very active at the human

    female VNO, the only difference between the two being an alkene group at the 4th carbon.




    From logical deduction and

    quantitative structure-property relationships, I assert the following:

    A) An alkene group at the 3rd carbon of

    the skeletal molecule dramatically increases activity at the VNO

    B) A fully saturated group at the 16th-17th

    carbons also significantly increases activity.

    EPILOGUE: Therefore, it is my hypothesis that

    4-androsten-3-one, as a molecular hybrid containing the most desired substitutions may be very active at the human

    female VNO, more so than the archetypical androsta-4,16-dien-3-one. If possible I ask for you good folks within this

    esoteric paradigm to voice your opinion with respect to this hypothesis.
    Last edited by Archetypical Hybrid (HEC); 04-21-2006 at 06:47 PM.

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