Rhapontigenin is a natural compound that belongs to the stilbenoid family. It is found in various plants, including rhubarb, grapes, and peanuts. Rhapontigenin has gained significant attention in recent years due to its potential therapeutic and environmental applications. This paper aims to provide a comprehensive review of rhapontigenin, including its method of synthesis or extraction, chemical structure, biological activity, biological effects, applications, future perspectives, and challenges.
Q1: How Can I Obtain a Quote for a Product I'm Interested In?
To receive a quotation, send us an inquiry about the desired product.
The quote will cover pack size options, pricing, and availability details.
If applicable, estimated lead times for custom synthesis or sourcing will be provided.
Quotations are valid for 30 days, unless specified otherwise.
Q2: What Are the Payment Terms for Ordering Products?
New customers generally require full prepayment.
NET 30 payment terms can be arranged for customers with established credit.
Contact our customer service to set up a credit account for NET 30 terms.
We accept purchase orders (POs) from universities, research institutions, and government agencies.
Q3: Which Payment Methods Are Accepted?
Preferred methods include bank transfers (ACH/wire) and credit cards.
Request a proforma invoice for bank transfer details.
For credit card payments, ask sales representatives for a secure payment link.
Checks aren't accepted as prepayment, but they can be used for post-payment on NET 30 orders.
Q4: How Do I Place and Confirm an Order?
Orders are confirmed upon receiving official order requests.
Provide full prepayment or submit purchase orders for credit account customers.
Send purchase orders to sales@EVITACHEM.com.
A confirmation email with estimated shipping date follows processing.
Q5: What's the Shipping and Delivery Process Like?
Our standard shipping partner is FedEx (Standard Overnight, 2Day, FedEx International Priority), unless otherwise agreed.
You can use your FedEx account; specify this on the purchase order or inform customer service.
Customers are responsible for customs duties and taxes on international shipments.
Q6: How Can I Get Assistance During the Ordering Process?
Reach out to our customer service representatives at sales@EVITACHEM.com.
For ongoing order updates or questions, continue using the same email.
Remember, we're here to help! Feel free to contact us for any queries or further assistance.
Quick Inquiry
Note: Kindly utilize formal channels such as professional, corporate, academic emails, etc., for inquiries. The use of personal email for inquiries is not advised.
5-(4-Chlorophenyl)-1-(2,4-dichlorophenyl)-3-hexyl-1,2,4-triazole is a chemical compound that belongs to the class of triazole derivatives. It has gained significant attention in the scientific community due to its potential therapeutic and environmental applications. This paper aims to provide an overview of the synthesis, chemical structure, biological activity, and applications of 5-(4-Chlorophenyl)-1-(2,4-dichlorophenyl)-3-hexyl-1,2,4-triazole.
Arachidonamide, also known as anandamide, is an endogenous cannabinoid neurotransmitter that is synthesized in the brain and peripheral tissues. It is a member of the endocannabinoid system, which plays a crucial role in regulating various physiological processes, including pain, appetite, mood, and immune function. Arachidonamide is a lipid mediator that binds to cannabinoid receptors, CB1 and CB2, and exerts its effects through various signaling pathways.
N-(2-methyl-2S-hydroxy-ethyl)arachidonoylamide, also known as NADA, is a naturally occurring endocannabinoid that is synthesized in the body. It belongs to the family of N-acylethanolamines and is structurally similar to anandamide, another endocannabinoid. NADA has been found to have various biological activities and potential therapeutic applications.
S-1 Methanandamide is a synthetic analog of the endocannabinoid anandamide, which is a naturally occurring lipid mediator that binds to cannabinoid receptors in the body. S-1 Methanandamide has been extensively studied for its potential therapeutic applications in various medical conditions, including pain, inflammation, and cancer. This paper aims to provide a comprehensive review of S-1 Methanandamide, including its method of synthesis or extraction, chemical structure and biological activity, biological effects, applications, future perspectives, and challenges.
Tetrahydromagnolol is a natural compound found in the bark of Magnolia officinalis, a traditional Chinese medicinal plant. It has been extensively studied for its potential therapeutic effects in various diseases, including cancer, inflammation, and neurological disorders. This paper aims to provide a comprehensive review of tetrahydromagnolol, including its method of synthesis or extraction, chemical structure and biological activity, biological effects, applications, future perspectives, and challenges.
Central cannabinoid (CB1) receptor antagonists may have potential in the treatment of a number of diseases such as neuroinflammatory disorders, cognitive disorders, septic shock, obesity, psychosis, addiction, and gastrointestinal disorders. (R)-SLV 319 is the inactive enantiomer of SLV 319 with 100-fold less affinity for the CB1 receptor. SLV 319 is a potent and selective CB1 receptor antagonist with Ki values of 7.8 and 7,943 nM for CB1 and peripheral cannabinoid (CB2) receptors, respectively. SLV 319 is less lipophilic (log P = 5.1) and therefore more water soluble than other known CB1 receptor ligands.
R-1 Methanandamide Phosphate is a synthetic analogue of the endocannabinoid anandamide, which is a naturally occurring lipid mediator in the human body. It is a potent agonist of the cannabinoid receptors CB1 and CB2, and has been shown to have a range of biological effects, including anti-inflammatory, analgesic, and neuroprotective properties. We will also explore the future perspectives and challenges in the use and study of this compound.
Apoptosis Inhibitor II, also known as NS3694, is a small molecule inhibitor that has been shown to inhibit apoptosis in various cell types. Apoptosis is a programmed cell death process that is essential for maintaining tissue homeostasis and eliminating damaged or abnormal cells. However, dysregulation of apoptosis can lead to various diseases, including cancer, neurodegenerative disorders, and autoimmune diseases. NS3694 has been studied for its potential therapeutic applications in these diseases.