Anabolics
Search More Than 6,000,000 Posts
Results 1 to 8 of 8
  1. #1
    jbol's Avatar
    jbol is offline Senior Member
    Join Date
    Dec 2003
    Location
    On the End of a Needle
    Posts
    1,814

    Oral Turanabol's Half Life

    Anybody know? Same as Var?

  2. #2
    soo2bhuge's Avatar
    soo2bhuge is offline Senior Member
    Join Date
    Jul 2004
    Location
    chi-town
    Posts
    1,385
    i've read that bodybuilders have taken this up to 5 days before the test. so i would imagine it being no more than 24-48hours.

  3. #3
    jbol's Avatar
    jbol is offline Senior Member
    Join Date
    Dec 2003
    Location
    On the End of a Needle
    Posts
    1,814
    Quote Originally Posted by soo2bhuge
    i've read that bodybuilders have taken this up to 5 days before the test. so i would imagine it being no more than 24-48hours.
    Just curious of when to start PCT.

  4. #4
    soo2bhuge's Avatar
    soo2bhuge is offline Senior Member
    Join Date
    Jul 2004
    Location
    chi-town
    Posts
    1,385
    i've been wondering the same cause i'm about to start my cycle as well. i have a website, but it's at home, i'll post it once i get it.
    by the way, what r u running it with?

  5. #5
    lzicc's Avatar
    lzicc is offline Senior Member
    Join Date
    Apr 2004
    Location
    The Gym
    Posts
    1,174
    I have 300 of these coming in for my next cycle and I can't wait to try them. I have heard great things aobut them.

    The half life is 16 hours of what I read.

    [The pharmacokinetics of Oral-Turinabol in humans]

    [Article in German]

    Schumann W.

    Institut fur Mikrobiologie und experimentelle Therapie (ZIMET), Jena.

    Disposition and excretion of the anabolic steroid Oral-Turinabol (1;4-chloro-17 alpha-methyl-androsta-1,4-diene-17 beta-hydroxy-3-one) were investigated in male volunteers. Following single p.o. and i.v. administration of the tritium-labelled compound the plasma concentration courses of total radioactivity (1 and 1-metabolites) and of the unchanged parent drug as well as the urinary excretion were estimated. From these data model independent pharmacokinetic parameters based on statistical moments were calculated. 1 is almost completely absorbed after p.o. administration of 10 mg per volunteer. Peak concentrations of total radioactivity and of 1 in plasma were reached about 3 h p.a. Irregularities observed in the plasma level profile following both p.o. and i.v. administration of 1 are due to a marked enterohepatic circulation. Orally given 1 is subject to a first-pass effect, resulting in a diminished systematic availability. The AUC-ratio of the unchanged drug and the total radioactivity of 1 : 13 shows the predominance of metabolites in plasma. After i.v. administration the disposition of unchanged 1 was found biphasically with a terminal half-life of 16 h. 1 and its metabolites are preferentially excreted via the kidneys. The urinary total radioactivity represented about 60% of the dose following both administrations. Due to its affinity to SHBG 1 is able to compete for the protein binding of testosterone , resulting in an increased plasma level of non protein-bound testosterone.

    PMID: 1798729 [PubMed - indexed for MEDLINE]
    Last edited by lzicc; 03-07-2005 at 06:08 PM.

  6. #6
    jbol's Avatar
    jbol is offline Senior Member
    Join Date
    Dec 2003
    Location
    On the End of a Needle
    Posts
    1,814
    Quote Originally Posted by lzicc
    I have 300 of these coming in for my next cycle and I can't wait to try them. I have heard great things aobut them.

    The half life is 16 hours of what I read.

    [The pharmacokinetics of Oral-Turinabol in humans]

    [Article in German]

    Schumann W.

    Institut fur Mikrobiologie und experimentelle Therapie (ZIMET), Jena.

    Disposition and excretion of the anabolic steroid Oral-Turinabol (1;4-chloro-17 alpha-methyl-androsta-1,4-diene-17 beta-hydroxy-3-one) were investigated in male volunteers. Following single p.o. and i.v. administration of the tritium-labelled compound the plasma concentration courses of total radioactivity (1 and 1-metabolites) and of the unchanged parent drug as well as the urinary excretion were estimated. From these data model independent pharmacokinetic parameters based on statistical moments were calculated. 1 is almost completely absorbed after p.o. administration of 10 mg per volunteer. Peak concentrations of total radioactivity and of 1 in plasma were reached about 3 h p.a. Irregularities observed in the plasma level profile following both p.o. and i.v. administration of 1 are due to a marked enterohepatic circulation. Orally given 1 is subject to a first-pass effect, resulting in a diminished systematic availability. The AUC-ratio of the unchanged drug and the total radioactivity of 1 : 13 shows the predominance of metabolites in plasma. After i.v. administration the disposition of unchanged 1 was found biphasically with a terminal half-life of 16 h. 1 and its metabolites are preferentially excreted via the kidneys. The urinary total radioactivity represented about 60% of the dose following both administrations. Due to its affinity to SHBG 1 is able to compete for the protein binding of testosterone , resulting in an increased plasma level of non protein-bound testosterone.

    PMID: 1798729 [PubMed - indexed for MEDLINE]

    good info......thanks bro

  7. #7
    lzicc's Avatar
    lzicc is offline Senior Member
    Join Date
    Apr 2004
    Location
    The Gym
    Posts
    1,174
    You bet. Glad I could help bro.

  8. #8
    soo2bhuge's Avatar
    soo2bhuge is offline Senior Member
    Join Date
    Jul 2004
    Location
    chi-town
    Posts
    1,385
    i guess i was late with mine. sorry jbol

Thread Information

Users Browsing this Thread

There are currently 1 users browsing this thread. (0 members and 1 guests)

Posting Permissions

  • You may not post new threads
  • You may not post replies
  • You may not post attachments
  • You may not edit your posts
  •