cas: 90147-43-6 Ashwagandha Extract
Ashwagandha, one of the most powerful herbs in Ayurvedic healing, has been used since ancient times for a wide variety of conditions, and is most well-known for its restorative benefits. In Sanskrit Ashwagandha means "the smell of a horse," indicating that the herb imparts the vigor and strength of a stallion, and has traditionally been prescribed to help people strengthen their immune system after an illness. Ashwagandha is frequently referred to as "Indian ginseng" because of its rejuvenating properties, even though botanically, ginseng and Ashwagandha are Unrelated.
Ashwagandha is an evergreen shrub that grows in Asia and Africa. It is commonly used for stress. There is little evidence for its use as an "adaptogen
Ashwagandha (Withania somnifera), also known as Indian Ginseng, is an herb used in Ayurveda, the traditional medicine of India. Its root has a horsey smell and is said to confer the strength and virility of a horse. In Sanskrit, ashva means “horse” and gandha means “smell.” Various parts of the plant are used, but the most common supplemental form is an extract of its roots.
Ashwagandha is classified as an adaptogen, meaning it’s purported to enhance the body’s resilience to stress. Rodent and cell culture studies suggest that ashwagandha provides a wide range of health benefits,[1][2] but there is a lack of direct evidence in humans to support most of these effects.
cas: 229971-81-7 Exherin TA
Molecular Formula: C22H34N8O6S2
Formula Weight: 570.69
CAS No.: 229971-81-7
Exherin is a small, cyclic pentapeptide vascular-targeting agent with potential antineoplastic and antiangiogenic activities.
Small volumes of Exherin (ADH-1), inhibitor vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
CBNumber: CB32622979
Chemical Name: ACHN 490
Molecular Formula: C25H48N6O10
Formula Weight: 592.68
CAS No.: 1154757-24-0
Plazomicin has in vitro activity against several multi-drug-resistant organisms, including carbapenem-resistant Enterobacteriaceae. It was Food and Drug Administration (FDA) approved to treat complicated urinary tract infections (cUTIs), including acute pyelonephritis, following phase II and III trials compared with levofloxacin and meropenem, respectively. Despite the FDA Black Box Warning for aminoglycoside class effects (nephrotoxicity, ototoxicity, neuromuscular blockade, and pregnancy risk), it exhibited a favorable safety profile with the most common adverse effects being decreased renal function (3.7%), diarrhea (2.3%), hypertension (2.3%), headache (1.3%), nausea (1.3%), vomiting (1.3%), and hypotension (1.0%) in the largest in-human trial.
Relevance to patient care and clinical practice:
Plazomicin will likely be used in the treatment of multi-drug-resistant cUTIs or in combination to treat serious carbapenem-resistant Enterobacteriaceae infections.
Conclusions:
Plazomicin appears poised to help fill the need for new agents to treat infections caused by multi-drug-resistant Enterobacteriaceae.
Plazomicin has been assigned susceptibility breakpoints from the U.S. Food and Drug Administration (FDA) and U.S. Committee on Antimicrobial Susceptibility Testing for Enterobacteriaceae: ⩽2 µg/mL10 and ⩽4 µg/mL,11 respectively. Susceptibility data for plazomicin from selected studies are displayed in Table 1. Plazomicin has demonstrated excellent activity against Enterobacteriaceae. In the two largest studies, the minimum inhibitory concentration of plazomicin needed to inhibit 50% and 90% of the tested isolates, respectively (MIC50/90) = 0.5 µg/mL / 2 µg/mL with % susceptibility of >95% in both studies. Against Klebsiella, Escherichia, Enterobacter, Serratia, and Citrobacter species, plazomicin exhibited MIC50/90 = 0.25–0.5 µg/mL / 0.5–1 µg/mL. Plazomicin activity against Proteus, Morganella, and Providencia species was considerably lower, MIC50/90 = 1–4 µg/mL / 2–8 µg/mL. In several of these large surveillance studies, all the other aminoglycosides tested demonstrated activity similar to plazomicin against Enterobacteriaceae. What separated plazomicin from the other aminoglycosides was its activity against isolates considered to be MDR and/or carbapenem-resistant. All other aminoglycosides demonstrated significantly lower activity against these isolates with the exception of Enterobacteriaceae expressing 16S rRNA methyltransferases, which conferred resistance to all aminoglycosides as discussed.12–15 These MDR isolates are known to carry numerous determinants of resistance against aminoglycosides, namely AMEs, which explain this sharp decline in activity.
cas: 942413-05-0 VKGILS-NH2 PAR-2(6-1)amide(human)
Chemical Name: VKGILS-NH2
Molecular Formula: C28H54N8O7
Formula Weight: 614.78
CAS No.: 942413-05-0
VKGILS-NH2 is a reversed amino acid sequence control peptide for SLIGKV-NH2 (protease-activated receptor 2 (PAR2) agonist). VKGILS-NH2 has no effect on DNA synthesis in cells
VKGILS-NH2 serves as the reversed amino acid sequence control peptide for SLIGKV-NH2, a protease-activated receptor 2 (PAR2) agonist. PARs are a group of G-protein-coupled receptors existing in several cell types. Up to date, four PAR members including PAR1 to 4 have been identified, cloned and designated. PAR2 is expressed in the respiratory and gastrointestinal tracts. It is suggested that the activation of PAR2 is closely correlated with inflammatory evens in various cells and tissues. PAR2 has also been identified to induce protease activation and therefore result in systemic hypotension.
In vitro: The PAR2 activating peptide AP (SLIGKV-NH2) and the reverse peptide control RP (VKGILS-NH2) were used in one study to reveal that PAR2 slightly enhanced mucin secretion by human bronchial epithelial cells in vitro. According to this study, compared to cells treated with VKGILS-NH2, exposure of cells to the synthetic PAR2 agonist peptide (SLIGKV-NH2) for 30 mins resulted in a weak but statistically significant increase in mucin secretion at concentrations of 100 and 1000M
cas: 1206161-97-8 Filgotinib GPLG0634
What is filgotinib?
Filgotinib, also known by the trade name Jyseleca, is a type of drug known as a JAK inhibitor. These drugs work by limiting the action of Janus kinase enzymes, which are involved in the inflammation that causes the symptoms of rheumatoid arthritis and some other conditions.
Filgotinib isn’t a painkiller, but it can reduce the symptoms and limit the joint damage that could be caused by your condition. If filgotinib works for you, your symptoms should start to improve within the first 12 weeks after you start to take it, and possibly sooner. But you may not notice the full benefit for the first 6 months of treatment.
Filgotinib won’t be started if:
your condition isn’t active
you haven’t tried other treatments for your condition first
you have an infection.
Before you’re prescribed filgotinib, doctors may use a scoring system to assess how many of your joints are painful or swollen and how you are feeling. This helps them work out how active your arthritis is. You’ll also need blood tests before treatment starts to see whether the drug is suitable for you.
Your doctor will need to check if you’ve previously been exposed to tuberculosis (TB). Even if you don’t have symptoms, the bacteria that cause TB may still be present in the body, and you may need a course of treatment to deal with this before starting filgotinib.
If you’ve ever had hepatitis you may need regular checks for this as filgotinib may increase the risk of the hepatitis coming back.
Filgotinib is usually prescribed alongside methotrexate unless there are reasons why you can’t take methotrexate. However, it's recommended that filgotinib should not be used alongside other immunosuppressive or biologic drugs or other JAK inhibitors.
Filgotinib is not recommended if you’re pregnant, planning to become pregnant or breastfeeding.
Your doctor may decide not to prescribe filgotinib if you’re taking certain other medicines, including statins and some drugs used to treat high blood pressure or heart problems, or if you’ve had or have any of the following conditions:
shingles
disease of the lungs, liver or kidneys
heart problems, high blood pressure, high cholesterol, or blood clots (deep vein thrombosis or pulmonary embolism)
stomach ulcers
cancer.
How is it taken?
Filgotinib is taken as a tablet once a day. Your doctor will advise on the dose for you. The tablets should be swallowed whole and taken with a glass of water, either with or without food. In some circumstances, your doctor may decide to alter the dose.
Try to take your dose at the same time each day – if you’re late taking it, just take it as soon as you remember. If you miss your daily dose completely, carry on with the usual dose the next day – do not double it. If you take more than the recommended dose by mistake, contact your doctor straight away.
Because it’s a long-term treatment, it’s important to keep taking filgotinib (unless you have severe side effects):
even if it doesn’t seem to be working at first
even when your symptoms improve (to help keep your condition under control).
Your doctor may decide to stop filgotinib and try another treatment if your symptoms haven’t improved very much after 6 months.