Saturday, 14 October 2017

HARMINE OR TELEPATHINE

Listing description
Harmine
98%
Synonym: 7-Methoxy-1-methyl-9H-pyrido[3,4-b]indole
·         CAS Number 442-51-3

·         Empirical Formula (Hill Notation) C13H12N2O

·         Molecular Weight 212.25
·          Beilstein Registry Number 178813

·          EC Number 207-131-4

·          MDL number MFCD00004958
·          PubChem Substance ID 24857229

Properties

Related Categories
InChI Key  
BXNJHAXVSOCGBA-UHFFFAOYSA-N
assay  
98%
mp  
262-264 °C(lit.)
Gene Information  
human ... CDC2(983), CYP2D6(1565)

Description

Biochem/physiol Actions

Central nervous system stimulant.
Bottomless glass bottle. Contents are inside inserted fused cone.

Application

Harmine was used as a donor in the fluorescence resonance energy transfer (FRET) study between harmine and silver nanoparticles (AgNPs)[2].

General description

The combination index (CI, serves as a quantitative indicator of pharmacological interactions) for harmaline/harmine and methylene blue/harmine was studied[

Harmine, also known as telepathine, is a fluorescent harmala alkaloid belonging to the beta-carboline family of compounds. It occurs in a number of different plants, most notably the Middle Eastern plant harmal or Syrian rue (Peganum harmala) and the South American vine Banisteriopsis caapi (also known as "yage" or "ayahuasca").
Detailed description
 Harmine reversibly inhibits monoamine oxidase A (MAO-A), an enzyme which breaks down monoamines, making it a RIMA. Harmine selectively binds to MAO-A but does not inhibit the variant MAO-B.

Uses

Monoamines include neurotransmitters (serotonin, dopamine), hormones (melatonin, epinephrine, norepinephrine) and psychedelic drugs (psilocybin, DMT and mescaline). By slowing the breakdown of neurotransmitters, monoamine oxidase inhibitors (MAOIs) can help to replenish the body's supply of these chemicals, and many MAOIs are used as antidepressants. Harmine has not been the subject of much clinical research in the treatment of depression, which could be due in part to its restricted legal status in many countries, as well as the existence of synthetic MAOIs with fewer side effects.
P. harmala and B. caapi are both traditionally used for their psychoactive effects. B. caapi has a tradition of use in conjunction with plants containing the drug DMT. Traditionally, B. caapi is consumed as a drink, with or without the DMT-bearing plants (see Ayahuasca). Ordinarily, DMT is not active when taken orally, but users report very different effects when MAOIs are present in such beverages. Harmine and substances containing it have been used in conjunction with many other drugs by modern experimenters. Many hallucinogens appear to exhibit increased potency when used in this way.
Harmine is also a useful fluorescent pH indicator. As the pH of its local environment increases, the fluorescence emission of harmine decreases.
With the radioisotope carbon-11 harmine is used in positron emission tomography neuroimaging to examine its binding to MAO-A.[7]
Harmine found in root secretions of Oxalis tuberosa has been found to have insecticidal properties.[8]
Harmine has been found to increase EAAT2 glutamate pump expression in central nervous system, therefore reducing glutamate toxicity.

Anticancer

"Harmine showed cytotoxicity against HL60 and K562 cell lines. This could explain the cytotoxic effect of P. harmala on these cells."

Effects on bone and cartilage

"Harmine was shown to promote differentiation of osteoblasts (bone-forming cells), and chondrocytes (cells in the cartilage)."
It was also shown to inhibit osteoclastogenesis (the formation of bone resorbing cells)

Packaging

1 g in glass bottle

PRICE

$87233.81/KG OR $39651.73/IB

For more information:

mobile: +2348039721941

contact person: emeaba uche

e-mail: emeabau@yahoo.com



Tuesday, 10 October 2017

BETAINE[(CH3)3N+CH2COO- ]

·         CAS Number 107-43-7

·         Linear Formula (CH3)3N+CH2COO-

·         Molecular Weight 117.15
·          Beilstein Registry Number 3537113

·          EC Number 203-490-6

·          MDL number MFCD00012123
·          PubChem Substance ID 24891663

A betaine  in chemistry is any neutral chemical compound with a positively charged cationic functional group such as a quaternary ammonium or phosphonium cation (generally: onium ions) which bears no hydrogen atom and with a negatively charged functional group such as a carboxylate group which may not be adjacent to the cationic site.
Detailed description
A betaine thus may be a specific type of zwitterion. Historically the term was reserved for TMG (trimethylglycine) only. Biologically, betaine is involved in methylation reactions and detoxification of homocysteine.
The pronunciation of the compound reflects its origin and first isolation from sugar beets (Beta vulgaris subsp. vulgaris), and does not derive from the Greek letter beta (β). However, it is often pronounced beta-INE or even BEE-tayn.[1]
In biological systems, many naturally occurring betaines serve as organic osmolytes, substances synthesized or taken up from the environment by cells for protection against osmotic stress, drought, high salinity or high temperature. Intracellular accumulation of betaines, non-perturbing to enzyme function, protein structure and membrane integrity, permits water retention in cells, thus protecting from the effects of dehydration. It is also a methyl donor of increasingly recognised significance in biology.

Commercial uses

Phosphonium betaines are intermediates in the Wittig reaction.
The addition of betaine to polymerase chain reactions improves the amplification of DNA by reducing the formation of secondary structure in GC-rich regions. The addition of betaine has been reported to enhance the specificity of the polymerase chain reaction by eliminating the base pair composition dependence of DNA melting.

PRICE

$230/KG OR $104.54/IB

For more information:

mobile: +2348039721941

e-mail: emeabau@yahoo.com


contact person: emeaba uche




BENZYL BENZOATE(BnBzO)[ C14H12O2]

·         CAS Number 120-51-4

·         Linear Formula C6H5COOCH2C6H5

·         Molecular Weight 212.24
·          Beilstein Registry Number 2049280

·          EC Number 204-402-9

·          MDL number MFCD00003075
·          PubChem Substance ID 57653953

Benzyl benzoate (BnBzO), sold under the brand name Scabanca among others, is a medication and insect repellant.[1] As a medication it is used to treat scabies and lice.[2] For scabies either permethrin or malathion is typically preferred.[3] It is applied to the skin as a lotion. Typically two to three applications are needed.
Detailed description
Side effects may include irritation of the skin.[2] It is not recommended in children.[3] It is also used in other animals; however, is toxic to cats.[1] How it works is unclear.[4]
Benzyl benzoate was first studied medically in 1918.[1] It is on the World Health Organization's List of Essential Medicines, the most important medication needeIt is on the World Health Organization's List of Essential Medicines, the most effective and safe medicines needed in a health system.[5] Benzyl benzoate is available as a generic medication.[3] The wholesale cost in the developing world is about 0.21 to 0.53 USD per 100 mls.[6] It is not available for medical use in the United States.[1] In the United Kingdom it costs the NHSabout 2.50 pounds for 500 mLs.

Uses

Medical

Benzyl benzoate is an effective and inexpensive topical treatment for human scabies.[7] It has vasodilating and spasmolytic effects and is present in many asthma and whooping cough drugs.[8] It is also used as an excipient in some testosterone-replacement medications (like Nebido) for treating hypogonadism.[9]
Benzyl benzoate is used as a topical acaricidescabicide, and pediculicide in veterinary hospitals.[10]

Non-medical


Benzyl benzoate is used as a repellent for chiggers, ticks, and mosquitoes.[10] It is also used as a dye carrier, solvent for cellulose derivatives, plasticizer, and fixative in the perfume industry.

PRICE
$127.87/KG OR $58.12/IB

For more information:

mobile: +2348039721941

e-mail: emeabau@yahoo.com


contact person: emeaba uche