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Tritium
Our associated TRITIUM LABELING Lab from the
Russian Academy
of Sciences in Moscow, Russia is highly qualified,
very specialized and ready to handle any known tritium
labeling procedures and/or techniques.
Among the methods and/or approaches used are:
-
Catalytic reduction with tritium
gas – specific
labeling
-
Catalytic dehalogenation with
tritium gas –
specific labeling
-
Exchange reactions using tritium
gas – random
labeling
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Exchange reactions using
tritiated water –
random labeling
-
Chemical and enzymatic reactions
– specific and
random labeling
Examples of Specific Procedures
-
High Temperature Solid state Catalytic Isotope Exchange (HTSCIE)
with Tritium gas:
the compound to be labeled is coated on a solid Pd or Pt
catalyst, exposed to tritium gas at a given optimum temperature
and pressure, then eluted and isolated via preparative HPLC.
-
Palladium Oxide Catalyzed Tritium Exchange (POCTE):
a proprietary method similar to above.
-
Combination of above tritiation procedures of an appropriate
chemical precursor to the desired final compound followed by the
full chemical or enzymatic synthesis of the desired final
product.
Comments
-
We can
label virtually any compound that has catalytically exchangeable or
chemically replaceable hydrogen atoms,
by choosing from the above methods the one
that will better preserve the chemical integrity and the biological
activity of the given compound.
-
The variety of
the
classes of compounds
that we succeeded to label ranged from “small
but reactive molecules” to
Peptides, Proteins, Oligonucleotides, and Macrocyclic complex
biologically active compounds.
We were quite successful in labeling these complex molecules at high
specific activities where our competitors could not succeed.
-
We also
specialize in labeling
Proprietary Compounds
under the strict rules of Confidentiality Agreements required by our
clients (for obvious reasons these compounds are not listed below).
-
When catalytic
exchange reactions are to be used for highly confidential compounds,
we do not need ask for the full
disclosure of the structure of the compound. We would need to know
the
only the general characteristics of
the molecule such as number of sulphur containing functional groups,
S-S bridges, epoxy groups that could hinder the labeling or other
reactive functional groups that might not withstand the tritiation
reactions we might contemplate to apply.
- All
orders are custom made for a minimum amount of one mCi
or more where applicable due to the low mass/high specific activity
relationship for given compound. If needed, larger amounts of
labeled material can also be prepared either by choosing different
methods or via repetitive batches.
-
All products are being purified by preparative HPLC and finally
analyzed using HPLC and other chromatographic methods.
-
Our products
have a
Chemical and Radiochemical Purity
of at least 97% by HPLC or higher if you so desire.
-
Where
applicable, our Lab could also
custom synthesize medium size non labeled proprietary peptides
containing unsaturated functional groups that upon saturation with
tritium will lead to the desired specific tritium labeled compounds
or to subject them to their tritiation via random labeling.
-
Enzymatic reactions have also been used for the labeling of some
complex biologically active molecules, followed by the tedious
preparative HPLC separation of the desired product from the complex
reaction mixture (see the various alkyl Coenzyme A derivatives;
Rapamycine; Leukotriene B4, etc.).
ORDERING
Please check the
List of Compounds from below for the names of all tritium labeled
compounds that we MADE OVER THE PAST 15 YEARS as custom syntheses. These
compounds were prepared as a result of specific requests from specific
customers. Because of that and the limited stability upon storage of
high specific activity tritium labeled organic molecules, the listed
compounds are not available from stock and have to be synthesized each
time anew in a minimum amount of one milliCurie.
Upon ordering, please
specify the name of the compound; the desired amount, specific activity
and purity; the HPLC system (if any) that you prefer and the shipping
solvent desired. If you do not find your compound below, please
inquire with us by email, phone or fax.
The catalytic
tritium exchange reactions always lead to a random distribution of the
tritium atoms in the molecule. Our associated Tritium Lab does not offer
Tritium NMR services. However, should the distribution of the tritium
atoms be of importance to you, our Lab could prepare an additional one
milliCurie sample for a Tritium NMR analysis to be done either by your
company or by another analytical lab. Usually our lab can prepare such a
sample for a minimal or at no additional charge, depending upon the
compound and size of your order. This sample will be packed in a
separate vial and shipped to you together with your order that you could
send to the lab that will do the NMR spectrum. We can facilitate this
service for you for an additional charge of $ 2000 to $ 3000 to be
billed directly to you by given service lab, if you so desire.
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Code |
Compound |
Specific Activity |
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CHT-304 |
(+)Abscisic acid [3H(G)] |
>10 Ci/mmol |
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CHT-001 |
Acetic acid (1-3H) |
>15 Ci/mMol |
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CHT-002 |
Acetic acid (1,2-3H) |
>15 Ci/mmol |
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CHT-350 |
N-Acetyl-hydroxy-proline, L-4[3H(G)] |
>15 Ci/mmol |
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CHT-351 |
N-Acetyl-D-lactosamine,[glucosamine
6-3H] |
>30 Ci/mmol |
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CHT-012 |
Adenine (8-3H] |
>10 Ci/mmol |
|
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CHT-004 |
Adenine (2,8-3H) |
>40 Ci/mmol |
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CHT-005 |
Adenosine (8-3H) |
>40 Ci/mmol |
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CHT-006 |
Adenosine (2,8-3H) |
>20 Ci/mmol |
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CHT-007 |
Deoxyadenosine
(2,8-deoxyribose-U-3H) |
>20 Ci/mmol |
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CHT-008 |
Deoxyadenosine
(2,8-deoxyribose-U-3H)-5'-triphosphate |
>15 Ci/mmol |
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CHT-009 |
Adenosine (8-3H)-5'- monophosphate
(lithium salt) |
>15 Ci/mmol |
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CHT-201 |
Adenosine (8-3H)-5'-diphosphate |
>15 Ci/mmol |
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CHT-202 |
Adenosine (8-3H)-5'-triphosphate |
>15 Ci/mmol |
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CHT-010 |
[8-3H] Adenosine 5'-monophosphate |
>15 Ci/mmol |
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CHT-011 |
[8-3H] Adenosine 5'-diphosphate |
>15 Ci/mmol |
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CHT-013 |
[8-3H] Adenosine 5'triphospate |
>15 Ci/mmol |
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CHT-352 |
Aflatoxin M1, [3H(G)] |
>2 Ci/mmol |
|
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CHT-353 |
Agmatine, [2,3,4,5-3H] |
>50 Ci/mmol |
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CHT-016 |
L-Alanine (2,3-3H) |
>30 Ci/mmol |
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CHT-305 |
D-Alanine-D-Alanine [2,3-3H] |
>20 Ci/mmol |
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CHT-305B
|
L-Alanine-L-Alanine [2,3-3H] |
>30 Ci/mmol |
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CHT-354 |
Alanine, beta-[2,3-3H] ethylester
HCl |
>20 Ci/mmol |
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CHT-355 |
Aldosterone, [1,2,6,7-3H] |
>50 Ci/mmol |
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CHT-356
|
Allylamine, [2,3-3H] |
>30 Ci/mmol |
|
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CHT-357 |
(±)-1-Amino-[4,5-3H]cyclopentane-trans-1,3-dicarboxylic acid |
>20 Ci/mmol |
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CHT-358 |
2-Amino-2-methyl-1-propanol-[1-3H] |
>45 Ci/mmol |
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CHT-373 |
Amphotericin (3H) |
6.5 Ci/mmol |
|
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CHT-359
|
Anandamide,
[arachidonyl-5,6,8,9,11,12,14,15-3H] |
>160 Ci/mmol |
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CHT-360
|
Androsterone [9,11-3H] |
>40 Ci/mmol |
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CHT-361
|
Antipyrine, [3H(G)] |
>20 Ci/mmol |
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CHT-022 |
Arachidonic Acid
[5,6,8,9,11,12,14,15-3H] |
>100 Ci/mmol |
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CHT-366 |
2-Arachidonyl Coenzyme
A,[arachidonyl-5,6,8,9,11,12,14,15-3H] |
>200 Ci/mmol |
|
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CHT-367 |
Arachidonyl
glycerol,[arachidonyl-5,6,8,9,11,12,14,15-3H] |
>100 Ci/mmol |
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CHT-368 |
Arachidonyl-4-hydroxyphenylamide [arachidonyl
5,6,8,9,11,12,14,15-3H] |
>200 Ci/mmol |
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CHT-203 |
D or L-Arginine [2,3-3H] |
>40 Ci/mmol |
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CHT-203B |
D or L-Arginine [4,5-3H] |
>40 Ci/mmol |
|
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CHT-369 |
Asparagine, L-(3H) |
>100 mCi/mmol |
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CHT-032 |
D or L-Aspartic acid (2,3-3H) >10 Ci/mmol |
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CHT-370
|
Avermectin (3H) |
>2 Ci/mmol |
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CHT-371 |
Avermectin B1A, [5-3H] |
>15 Ci/mmol |
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CHT-372 |
Baclofen (-), [butyl-4-3H(N)] |
>30 Ci/mmol |
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CHT-021 |
3,4-Benzpyrene [3H (G)] |
>50 Ci/mmol |
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CHT-023 |
Benzyladenine [3H (G)] |
>100 Ci/mmol |
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CHT-205
|
BIIL-206 BS [3H] |
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