chemical-categories

 

Pharmaceutical Raw Material Griseofulvin For Health Skin Tinea Inhibition 126-07-8 

 

Griseofulvin Basic Info.：

 

Product Name: Griseofulvin

Synonyms: (+)-GRISEOFULVIN;GRISEOFULVIN;

CAS: 126-07-8 

MF: C17H17ClO6 

MW: 352.77 

EINECS: 204-767-4 

Chemical Properties: Crystalline Solid 

 

(+)-Griseofulvin Usage:

 

1.Adrenegic blocker, Ca channel blocker, coronary vasodilator, antiarrhythmic. 

2.Antifungal, inhibits mitosis in metaphase.

3.Griseofulvin is a spirobenzofuran produced by a number of Penicillium species, first isolated in the 1930s by Raistrick's group. Griseofulvin is a selective antifungal agent used to treat skin infections in animals and humans. Griseofulvin acts by binding to fungal tubulin and inhibiting the mitotic spindle. Griseofulvin's ability to bind to keratin is considered an important aspect of the metabolite's access to dermatophytic fungi. More recently, griseofulvin has become an important phenotypic marker in Penicillium taxonomy. 

4.It is an antifungal drug. It is used both in animal and in humans, to treat rigworm infections of the skin and nails. It is derived from the mold Penicillium griseofulvum.

 

 

Raw Pharmaceutical Powder Capecitabine For Antineoplastic Function CAS 154361-50-9 

 

Capecitabine Basic Info.:

 

Product name: Capecitabine

Synonym: 5-Deoxy-5-fluoro-N-[(pentyloxy)carbonyl]cytidine

Assay:99%

Molecular formula:C15H22FN3O6 

Molecular weight: 359.358

CAS number: 154361-50-9

Appearance: White or almost white crystalline powder.

Pharmacology: Capecitabine combine with Docetaxel treatment includes failure of anthracycline chemotherapy in metastatic breast cancer and the The transfer of single-agent first-line treatment of colorectal cancer

 

Capecitabine Application:

 

Capecitabine is a chemotherapy drug| that usually given to treat cancer of the colon, rectum|, breast|, stomach|, pancreas|and gullet| (oesophagus).

Capecitabine is a prodrug, that is enzymatically converted to 5-fluorouracil in the tumor, where it inhibits DNA synthesis and slows growth of tumor tissue. The activation of capecitabine follows a pathway with three enzymatic steps and two intermediary metabolites, 5'-deoxy-5-fluorocytidine (5'-DFCR) and 5'-deoxy-5-fluorouridine (5'-DFUR), to form 5-fluorouracil.

 

 

Ropivacaine Hydrochloride Ropivacaine Hcl 132112-35-7 Local Anesthetic Raw Material

 

Ropivacaine HCL Basic Info.:

 

Product Name: Ropivacaine hydrochloride

Synonyms: S-ROPIVACAINE HCL;

CAS: 132112-35-7

MF: C17H26N2O.ClH.H2O

MW: 328.88

EINECS: N/A

Product Categories: Chiral Reagents;Intermediates & Fine Chemicals;Pharmaceuticals

use:anesthetic (local),Pharmaceutical raw materials

Packing:Foil bag or as requirments

 

Ropivacaine HCL Description:

 

Ropivacaine is a local anaesthetic drug belonging to the amino amide group. The name ropivacaine refers to both the racemate and the marketed S-enantiomer. 

 

Ropivacaine is an anesthetic (numbing medicine) that blocks the nerve impulses that send pain signals to your brain. 

Ropivacaine is used as a local (in only one area) anesthesia for a spinal block, also called an epidural. The medication is used to provide anesthesia during a surgery or C-section, or to ease labor pains. 

Ropivacaine may also be used for purposes not listed in this medication guide.

 

Ropivacaine HCL Applications:

 

(1) Surgical anesthesia:Epidural anesthesia (including epidural anesthesia during cesarean section);Local infiltration anesthesia.

(2) Acute pain control:For postoperative or labor analgesia continuous epidural infusion can be used can also be intermittent medication;Local infiltration anesthesia.

 

 

White Powder Male Sex Enhancement Yohimbine HCL For Sex Protein Supplements 65-19-0

 

Yohimbine HCL Basic Info:

 

Product Name: Yohimbine Hydrochloride

Other name: Corynine; Aphrodine

Synonyms: Corynine Hydrochloride;Aphrodine Hydrochloride;Aphrosol Hydrochloride;Yohimbe HCL;Yohimbine HCL;Yohimbine Hydrochloride

CAS: 65-19-0

MF: C21H27ClN2O3

MW: 390.9

EINECS: 200-600-4

Purity: 99%

Melting point: 288-290 °C (dec.)(lit.)

alpha: 99 º (c=1%, H2O, dry subst)

refractive index: 103 ° (C=1, H2O)

storage temp.: Refrigerator

solubility: H2O: 10 mg/mL

Chemical Properties: white to slightly yellow powder

Usage: 

(1)Indole alkaloid with α2-adrenergic blocking activity. Mydriatic. Used in the treatment of neurological disorders.

(2)alpha adrenergic blocker, mydriatic, antidepressant

(3)vasodilator, neuromodulator

(4)a2-adrenergic antagonist, used for erectile dysfunction

(5)Erectile dysfunction & Mydriatic agent

Product Categories: Alkaloids;Biochemistry;Indole Alkaloids;Natural Plant Extract;Adrenoceptor;Adrenoceptors;Chiral Reagents;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals;API;chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract;ADENYL;Inhibitors.

 

Yohimbine HCL Description:

 

Yohimbine has been shown in human studies to be effective in the treatment of male impotence. Yohimbine has been shown to be effective in the treatment of orgasmic dysfunction in men. Yohimbine has also been used to treat hypoactive sexual desire disorder (reduced libido) in women. Increase muscular tension or urinary function no damage sex; Accelerate human body energy metabolism, increase energy supply.

 

Yohimbine has been used to facilitate recall of traumatic memories in the treatment of post traumatic stress disorder (PTSD). Use of yohimbine outside therapeutic settings may not be appropriate for persons suffering from PTSD. In pharmacology, yohimbine is used as a probe for α 2-adrenoceptor. In veterinary medicine, yohimbine is used to reverse anesthesia from the drug xylazine in small and large animals.

 

Yohimbine HCL Application:

 

Yohimbine readily penetrates the and produces a complex pattern of responses in lower doses than those required to produce peripheral alpha-adrenergic blockade. These include, anti-diuresis, a general picture of central excitation including elevation of blood pressure and heart rate, increased motor activity, nervousness, irritability and tremor. Sweating, nausea and vomiting are common after parenteral administration of the drug. Also, dizziness, headache skin flushing reported when used orally.

 

Generally, this drug is not proposed for use in females and certainly must not be used during pregnancy. Neither is this drug proposed for use in pediatric, geriatric or cardio-renal patients with gastric or duodenal ulcer history. Nor should it be used in conjunction with mood- modifying drugs such as antidepressants, or in psychiatric patients in general.

 

Renal diseases and patient's sensitive to the drug. In view of the limited and inadequate information at hand, no precise tabulation can be offered of additional contraindications. It is important that your doctor check your progress at regular visits to make sure that this medicine is working properly. Use yohimbine exactly as directed by your doctor. Do not use more of it and do not use it more often than ordered. If too much is used, the risk of side effects such as fast heartbeat and high blood pressure is increased.

 

 

Anabolic Steroids Raw Stenbolone Powder Methylstenbolone For Muscle Growth 5197-58-0

 

Methylstenbolone Basic Info.

 

Product Name: Methylstenbolone (Methyl Stenbolone)

Alias: Methylstenbolone;Methyl Stenbolone;Stenbolone;NSC 34418;NSC 65890;Stenebolone

CAS: 5197-58-0

Molecular Formula: C20H30O2

Molecular Weight: 302.455

Assay: 99.5%

Melting Point: 154-156°C

Storage temp.: Refrigerator

Packing: 1kg/foil bags

Package: foil bag or tin, or as you require

Properties: white powder

Product Categories: Intermediates & Fine Chemicals;Pharmaceuticals;Steroids

Usage: pharmaceutical intermediates.Nutritional Supplement.

 

Methylstenbolone Description:

 

MethylStenbolone is a very new and potent designer steroid recently brought to the market by Antaeus labs. Several products in the past have claimed to use this compound, however independent lab testing has revealed they only contained superdrol.

 

Methylstenbolone does not convert to an estrogenic metabolite or have any affinity for the progesterone receptor, so estrogen mediated side effects should be virtually non-existent. Methylstenbolone is also one of the most toxic substances available due to its ability to resist metabolization, although anecdotal reports lead us to believe it carries less side effects than superdrol.

 

ethylstenbolone is a DHT derived prohormone that provides lean mass gains with low water retention.

Methylstenbolone provides increases in mass, size, and strength. Unlike superdrol, Methylstenbolone retains little to no water retention meaning you can bulk up without losing definition. This will provide the lookof much fuller muscles. Many people after experiencing methylstenbolone prefer it over superdrol.MethylStenbolone is a powerful and extremely potent compound that has people in the steroid literally turned upside down.

 

Methylstenbolone is being called the "new superdrol." Compared to Superdrol,Methylstenbolone is more anabolic, rapidly increasing muscle size, density and strength. 

 

Methylstenbolone Applications:

 

Methylsten is a very strong compound therefore it's best to start with a lower dosage to asses tolerance and slowly increase it into the desired range. Methylsten cycles are typically 3-4 weeks in length with 4 weeks being the most common. Due to the extreme potency and toxicity of this compound use for longer than 4 weeks is not recommended. Below are two common dosing protocols:

Methylsten dosing for new users:  Week1:  4-8mg / per day | Week 2-3: 8mg / per day

Methylsten dosing for experienced users:  Week1: 8mg / per day | Week 2-3: 12mg / per day | Week 4: 16mg / per day

Methylsten works relatively quickly, therefore the majority of users typically begin to experience the effects within the first week. 

 

 

Androgenic Steroid Intermediate Methoxydienone Max LMG Raw Hormone Powder 2322-77-2 

 

Methoxydienone Basic Info.:

 

Product Name: Methoxydienone

CAS: 2322-77-2 

MF: C20H28O2 

MW: 300.44

EINECS: 219-034-4 

Assay: 90% min.

Packing: 1kg net/foil bag or 10kg net/tin.

Delivery: Express courier.

Character: White crystalline powder. 

Melting point: 150-160°C

Usage: 18-levonorgestrel,.Max LMG is a progestin derived steroid and not a 17-alpha alkylated steroid. Max LMG is structurally related to RU-486 and acts as an antiprogesterone, decreasing estrogen-like effects.

 

Methoxydienone Descriptions:

 

Methoxydienone particular to a process of synthesis of levonorgestrel, Levonorgestrel is a quick, short-term oral contraceptives, contraceptive mechanism is significantly inhibit ovulation and prevent embryo 

implantation, and to increase the consistency of the cervical mucus, sperm penetration resistance increases, and thus play a fast-acting contraception.

 

Max LMG is a progestin derived steroid and not a 17-alpha alkylated steroid. Max LMG is structurally related to RU-486 and acts as an antiprogesterone, decreasing estrogen-like effects.

 

Max LMG can cause rapid "wet" gains due to its progestogenic nature. Great for those needing fast weight gain and unconcerned about looking smooth or fat.

 

Methoxydienone Applications:

 

Methoxydienone is used for promoting the synthesis of protein and reduce the decomposition of amino acid, and for improving muscle hyperplasia, action and enhance male sexual characteristics.

 

Methoxydienone is often used in the medical practice activities chronic wasting disease.Max LMG is an excellent non methylated prohormone that provides muscle hardening and increased muscle mass.

 

Max LMG is progestin designed to give solid gains in muscle mass with low water retention. The progestational activity of methoxygonadiene (once it is converted to its active metabolites) is considered to be slightly stronger than nandrolone.

 

 

Anti Aging Estrogen Steroids Tibolone Livial For Female Hormones Medicines 5630-53-5

 

Tibolone Basic Info.

 

Product name: Tibolone

Alias: Liviella; Livial; Tibolone

CAS: 5630-53-5

MF: C21H28O2

MW: 312.45

EINECS: 227-069-1

Assay: 99% min.

Appearance: White or off-white crystal powder

Grade: Pharmaceutical Grade

Storage: Shading, confined preservation

Usage: It is a synthetic hormone-type drug which is used mainly for hormone replacement therapy in post-menopausal women.

 

Tibolone Description:

 

Tibolone (Livial/Liviella) is used mainly for treatment of endometriosis, as well as hormone replacement therapy in post-menopausal women. Tibolone is a synthetic steroid hormone drug, which is fairly non-selective in its binding profile, acting as an agonist mainly at estrogen receptors, with a preference for ER alpha. Tibolone has similar or greater efficacy compared to older hormone replacement drugs, but shares a similar side effect profile. It has also been investigated as a possible treatment for female sexual dysfunction.

 

Tibolone is a synthetic steroid hormone drug, which is fairly non-selective in its binding profile, acting as an agonist mainly at estrogen receptors, with a preference for ER alpha. It is used mainly for treatment of endometriosis,as well as hormone replacement therapy in post-menopausal women. Tibolone has similar or greater efficacy compared to older hormone replacement drugs, but shares a similar side effect profile.It has also been investigated as a possible treatment for female sexual dysfunction. 

 

Tibolone Applications:

 

Tibolone is an estrogen-like compound used for the treatment of the symptoms associated with menopausal transition (i.e., climacteric symptoms) and also for the treatment of osteoporosis.Three major metabolites of tibolone are responsible for its tissue selective mechanism of action. Conversion into 3α- and 3β-hydroxy-tibolone results in estrogenic effects in brain, vagina, and bone. The  isomer has progestrogenic and androgenic effects and does not cause estrogenic stimulation in the endometrium.A two-year longitudinal study indicates that low doses (1.25-2.5 mg) of tibolone effectively relieve climacteric symptoms and prevent loss of bone mass in early postmenopausal women.

 

 

Anti-Aging Properties Thyrotropin TRH Peptide Thyroid Stimulating Hormone 24305-27-9

 

Thyrotropin TRH Quick Details:

 

Product Name: Thyrotropin TRH

TRH (Thyrotropin Releasing Hormone) (Protirelin Acetate)

Synonyms:TRH;TRF;TRH,HUMAN;

Sequence: (pyro)Glu-His-Pro-NH2

CAS: 24305-27-9

MF: C16H22N6O4

MW: 362.38

EINECS: 246-143-4

Storage temp.: −20°C

Solubility: H2O: 10 mg/mL, clear, colorless

Appearance: Lyophilized Powder

PubChem: CID 439302

Product Categories: Peptide;Thypinone.

Usage: Prothyrotropin.

 

Product Description Of Thyrotropin TRH:

 

Anti-Aging Properties of Thyrotropin Releasing Hormone TRH By DR WALTER PIERPAOLI MD 2012 THE YEAR OF THE FOUNTAIN OF YOUTH MOLECULE - TRH - DR WALER PIERPAOLI MD - SWITZERLAND AND ITALIAN RESEARCH LABS AND CLINICS .. A4M AMERICAN ACADEMY OF ANTIAGING MEDICINE Aging-Reversing Properties of Thyrotropin Releasing Hormone (TRH) Walter Pierpaoli, MD, PhD Interbion Foundation for Basic Biomedical Research (TRH Absrtact)

 

Product Application Of Thyrotropin TRH:

 

Previous work from our laboratory prompted us to study the effects of short-term, acute administration of TRH or its chronic oral administration, on organs, tissues and aging-related metabolic and hormonal markers, in order to acquire more knowledge on effects, dosage and timing of administration according to its circadian cyclicity. In addition, we wanted to verify its anti-aging effects on two most fundamental functions, namely gonadal- reproductive and kidney-urinary. The results demonstrate that both a short-term, acute or a chronic, long-term oral administration of TRH to old, aging mice, results into positive changes and rapid correction to more juvenile levels of most typical aging-related hormonal and metabolic alterations.

 

Thyrotropin TRH Function:

 

Store the kit at 4°C upon receipt.The kit should be equilibrat4ed to room temperature before the assay. Remove any unneeded strips from Human MUSK Antibody-Coated plate, reseal them in zip-lock foil and keep at 4°C.

Precipitates may appear in concentrated washing buffer. Please heat the buffer to dissolve all the precipitates, which will not affect the results.

Accurate pipette should be used to avoid experimental error. Samples should be added to the Microplate in less than 5 minutes. If a large number of samples are included, multiple channel pipette is recommended.

Standard curve should be included in every assay. Replicate wells are recommended. If the OD value of the sample is greater than the first well of standards, please dilute the sample (n times) before test. When calculating the original MUSK? concentration, please multiply the total dilution factor (XnX5).

 

 

Fat Loss Steroids Powder Sodium 2,4-Dinitrophenol Powders DNP For Medicine 1011-73-0

 

Sodium 2,4-Dinitrophenol Basic Info.:

 

Product Name: Sodium 2,4-Dinitrophenol

Synonyms: Sodium 2,4-Dinitrophenate;Sodium-2,4-Dinitrophenol;Sodium 2,4-Dinitrophenolate;2,4-Dinitrophenol Sodium Salt;2,4-Dinitro-Phenosodiumsalt;Dinitrophenol Sodiumsalt.

Alias: DNP

CAS No: 1011-73-0

MF: C6H3N2NaO5

MW: 206.09

EINECS: 213-786-7

Purity: 98%

Appearance: Yellow crystalline powder

Product Categories: Intermediates of Dyes and Pigments;Dyestuff Intermediates.

Usage: Weight loss drug.

 

Descriptions Of Sodium 2,4-Dinitrophenol:

 

Sodium 2,4-Dinitrophenol belongs to a small class of compounds that in many ways, while not 100% accurate can be labeled as manufactured toxins.It's mode of action, while strong is relatively simple by which the substance uncouples oxidative phosphorylation thereby increasing both body temperature and overall metabolic rate.So how does this work exactly?By its very nature DNP readily and rapidly destroys ATP, in-fact it thrives and fuels off of it and literally drains your muscle stores of all ATP.By this action the mitochondria are necessarily required to create more ATP to meet desired function or perhaps in most simplistic terms convert food into ATP.

 

To understand the benefits of DNP we really only need to say two words, "Fat Loss" beyond that there is no other benefit to this synthetic chemical.When you examine many of the other profiles here you'll find that most all anabolic steroids have a multitude of purposes as well as several of the non-steroidal compounds such as SERM's, AI's and Peptides, as well as many secondary functions;That simply isn't the case with DNP.When it comes to DNP we are not talking about an anabolic steroid, it is often talked about in conjunction, as both are generally and necessarily used at the same time but a steroid it is not.When we talk about DNP the truth is very simple, we're talking about fat loss plain and simple but when steroids are added we are assuredly talking about pure fat loss and not simple body weight loss.

 

Sodium 2,4-Dinitrophenol Applications:

 

DXM is also used recreationally.

 

Commercial Sodium 2,4-Dinitrophenol is primarily used as an antiseptic. It is a precursor to sulfur dyes. DNP is a chemical intermediate in the production of some herbicides including dinoseb and dinoterb. It has also been used to make photographic developer and explosives.

 

When exceeding label-specified maximum dosages, dextromethorphan acts as a dissociative hallucinogen. Its mechanism of action is via multiple effects, including actions as a nonselective serotonin reuptake inhibitor and a sigma-1 receptor agonist. The major metabolite of DXM, dextrorphan, also acts as an NMDA receptor antagonist. In high doses this produces effects similar to, yet distinct from, the dissociative states created by other dissociative anaesthetic. As well, the metabolite 3-methoxymorphinan of dextrorphan (thus a second-level metabolite of DXM) produces local anesthetic effects in rats with potency above dextrorphan, but below that of DXM.