[Latin Name] Trifolium pratensis L.

[Specification] Total isoflavones 20%; 40%; 60% HPLC

[Appearance] Brown to tan fine powder

Plant Part Used: Whole herb

[Particle size] 80Mesh

[Loss on drying] ≤5.0%

[Heavy Metal] ≤10PPM

[Storage] Store in cool & dry area, keep away from the direct light and heat.

[Shelf life] 24 Months

[Package] Packed in paper-drums and two plastic-bags inside.

[Net weight] 25kgs/drum

[What is Red Clober]

Red clover is a member of the legume family – the same class of plants where we find chickpeas and soybeans. Red clover extracts are used as dietary supplements for their high content of isoflavone compounds – which possess weak estrogenic activity and have been associated with a variety of health benefits during menopause (reduction of hot flashes, promotion of heart health and maintenance of bone density).

[Function]

1. Red Clover Extract can Improving health, anti-spasm, known for healing properties.

2. Red Clover Extract can Treating the skin diseases (such as eczema, burns, ulcers, psoriasis),

3. Red Clover Extract can Treating respiratory discomfort (such as asthma, bronchitis, intermittent cough)

4. Red Clover Extract can Owning anti-cancer activity and prevention of prostate disease.

5. Red Clover Extract can Most valuable of its estrogen-like effect and alleviate breast pain suffering.

6. Red Clover Extract can Contained red clover isoflavones plays in a weak estrogen, estrogen reduces the number and thusalleviate the suffering.

7. Red Clover Extract can Maintaining bone mineral density in postmenopausal women

8. Red Clover Extract can Raising high density lipoprotein cholesterol.

Can natural performance enhancers boost desire, improve orgasms, and give couples a more exciting sex life? In this couples experiment, couples test herbal viagra and libido boosters and report back.
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The secrets out: love ain’t easy and relationships are hard. Sexy time isn’t always as sexy as you want it to be. Or maybe sexy time doesn’t happen enough. Or… we all get it. If you’re a boyfriend or a girlfriend, you know that sometimes sex isn’t everything it’s cracked up to be. Your sex drive may not exactly sync up. Orgasms don’t always come easy (pun intended). Your taste in porn might not match. Or she might desire a man in a gorilla costume while you desire hot sex talk in French. These kinds of things can lead to relationship problems for some couples. Hopefully you and your other’s quirks match up in that weird magical way (relationship goals) BUT when they don’t…maybe those shiny bright boxes you spied at the bodega call your name. Well, in this experiment three cute couples try those wacky looking herbal performance enhancing drugs out…basically so you don’t have to.

Moof’s Medical Biochemistry Video Course: https://moof-university.thinkific.com/courses/medical-biochemistry-for-usmle-step-1-exam

For Related Practice Problems with Worked Video Solutions on Carbohydrates, visit courses.moofuniversity.com.

In this video, I introduce the topic of carbohydrates / sugars.

(CH2O)n is the general formula for a monosaccharide or simple sugar. Glucose (C6H12O6) is a very common and very important example.

Carbohydrate names end in “-ose”
Aldoses have aldehydes in their straight-chain forms (depicted as Fischer projections)
Ketones have ketones in their straight-chain forms (depicted as Fischer projections)

There are D sugars and L sugars, and the convention is based on the Fischer projections of D-glyceraldehyde and L-glyceraldehyde. The two are enantiomers because they are opposite in absolute configuration at all of their chiral centers (which, in this case, is only one). D-glyceraldehyde has an OH on the right, while L-glyceraldehyde has an OH on the left. Sugars that have their last OH on the right are D sugars; sugars that have their last OH are L sugars. Most sugars that exist in life forms are D sugars.

In the video, I depict the difference between Fischer projections (straight chain sugars) and Haworth projections (sugars in their ring forms). I also briefly mention the idea of anomers as a class of epimers, which are a specific class of diastereomers.

Diastereomers are stereoisomers that differ in at least one, but not all chiral centers.
Epimers are stereoisomers that differ at only one chiral center (they are a subclass of diastereomers).
Anomers are stereoisomers that differ at only one chiral center when that chiral center is specifically the anomeric carbon, the stereocenter that forms when a sugar forms a ring. Anomers are a subclass of epimers.

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