The very same thing on the US Amazon is $35. Not including probable tax when shipping to Europe.It's certainly a lot cheaper on amazon.com in the US.
As I said before, keep an eye out because soon there might be something cleaner on the market in the UK. If all goes to plan, the idea is to have a source which is reasonably priced and available in Europe.The very same thing on the US Amazon is $35. Not including probable tax when shipping to Europe.
I've been looking for a reasonably priced source in continental Europe but so far no luck.
Also, the products are two separate things. The on Laura linked is 60 caps, and the other that your showing above is 250 capsI see Should have searched more thoroughly with different parameters before making the claim. Thank you, Laura. My original search for Ecological Formulas thiamin only gave me this:
View attachment 30726
Then, after seeing your post, I searched for 'allthiamin' only (without typing the brand name) and the one you found popped up. But it says 'no delivery to your location'. Perhaps general search from my pc automatically omits results that are not available for shipping to my country.
Keyhole, have you compared Allithiamine with Sulbutiamine? Sulbutiamine is commonly sold as a nootropic and is also able to cross the blood brain barrier.
Eva TM says:
July 31, 2018 at 5:34 pm
Hi, Dr. Lonsdale, I need to ask something:
Can I take sulbutiamine instead of allithiamine? Both are thiamine disulfide if I’m not wrong. Allithiamine causes me intestinal pain (I have many intolerances and gastritis frequently, maybe its for garlic, i dont know), however, sulbutiamine does not hurt me. What is the difference between the two? Have both same effective? If your answer is affirmative: do I have to take the same dose of sulbutiamine as allithiamine? That is to say 50 mg sulbutiamina rising little by little up to 200-300mg?
In summary, my question is whether I can follow his guidelines and Dr. Lonsdale with sulbutiamine instead of allithiamine, or would have to change something
(I am taking with breakfast, with food. My stomach is very sensitive and I usually have this type of problem. I would be very grateful if you could resolve the doubt when you know it. It is very important for me to be able to do the treatment correctly)
Thank you very much
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Derrick Lonsdale says:
August 1, 2018 at 3:03 pm
Yes, I have never used it but it is also an open ring form of thiamine
Thiamine itself contains one sulfur atom, so Allithiamine actually has an extra sulfur molecule whereas sulbutiamine has no extra sulfur. What that extra sulfur does after it is left over from the conversion to thiamine I don't know. The conversion takes place after the molecule crosses the blood brain barrier, so it would seem that the sulfur ends up roughly the same place the thiamine ends up (perhaps in the same cell?). I'm not a biochemist though.
Once in the brain, sulbutiamine can be easily metabolized to thiamine. Look at the structure of sulbutiamine and here is what happens:
- reductively break the disulfide bond and form two identical mercaptans
RS−SR−→[H] 2 RS−H
- protonate the acetyl (that's on the nitrogen that will become part of our thiazole ring) oxygen to make it more attractive to nucleophilic substitution
- Let the mercaptan sulfur nucleophilically attack the acetyl carbonyl carbon
- eliminate water and form the 5-membered thiazole ring and we now have thiamine
What may be of some importance is the disposal of the prosthetic group that is evolved from any of these derivatives. The mercaptan derived from the disulfide derivatives, that is left outside the cell membrane as the complete molecule is hydrolyzed to deliver thiamine into the cell, has been well studied for its metabolic breakdown (108–112). Its pharmaceutical effect, if any, is unknown.
https://en.wikipedia.org/wiki/Thiol said:Many thiols have strong odors resembling that of garlic or rotten eggs. Thiols are used as odorants to assist in the detection of natural gas (which in pure form is odorless), and the "smell of natural gas" is due to the smell of the thiol used as the odorant. Thiols are sometimes referred to as mercaptans.[3][4] The term "mercaptan" /mərˈkæptæn/[5] was introduced in 1832 by William Christopher Zeise and is derived from the Latin mercurium captāns (capturing mercury)[6] because the thiolate group (RS−) bonds very strongly with mercury compounds.[7]