Wuhan Demeikai Biotechnology Co., Ltd

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Wuhan Demeikai Biotechnology Co., Ltd

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Pharmaceutical Intermediates Miconazole Nitrate Purity 99% with Best Wholesale Price

Pharmaceutical Intermediates Miconazole Nitrate Purity 99% with Best Wholesale Price CAS NO.22832-87-7

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  • Min.Order: 1 Kilogram
  • Payment Terms: L/C,D/A,D/P,T/T,Western Union,MoneyGram
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    USP(1-100)KilogramUSP(100-1000)KilogramCP(1-100)Kilogram

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Keywords

  • Miconazole Nitrate
  • Miconazole Nitrate Powder
  • Steriod

Quick Details

  • ProName: Pharmaceutical Intermediates Miconazol...
  • CasNo: 22832-87-7
  • Molecular Formula: C18H15Cl4N3O4
  • Appearance: White powder
  • Application: Only for Research Use
  • DeliveryTime: 3
  • PackAge: Drum
  • Port: SHANGHAI
  • ProductionCapacity: 3000 Kilogram/Day
  • Purity: 99
  • Storage: Dry storage
  • Transportation: air transport /Ocean Shipping
  • LimitNum: 1 Kilogram
  • Related Substances: 《0.1%
  • Residue on Ignition: 《0.1%
  • Heavy Metal: 《0.1%
  • Valid Period: 《0.1%
  • monthly production: 20kg
  • Customs code: 29000000

Superiority

name:miconazole nitrate 
cas:22832-87-7 
formula:c18h15cl4n3o4
molecular weight:479.16
synonyms:
nitric acid;conofite;1h-imidazole,1-[2-(2,4-dichlorophenyl)-2- [(2,4-dichlorophenyl)methoxy]ethyl]-,mononitrate;gyno-monistat;micatin;imidazole,mononitrate;florid,mononitrate;daktarin;aflorix;miconazol nitrate;
einecs:245-256-6
density:1.451g/cm3
melting point:170-185 °c
boiling point:555.1 °c at 760 mmhg
flash point:289.5 °ca
appearance:white crystal powder
assay: 98.5-101.5(%)
package: as per your requirement
storage: dry
application: antibiotic resistance to infection api.
 
 
miconazole nitrate description:
 
miconazole nitrate is a kind of antifungal agent which is the drug "dakelin" which we are familiar with as commonly used drugs for treating skin ringworm. it has various kinds of effects. it inhibit the biosynthesis of ergosterol which is the fungal cell membrane component, causing damage to the cell membrane structure, increasing the membrane permeability, resulting in the leakage of the intracellular components and inhibiting the glucose utilization, preventing the nutrient uptake, and finally leading to fungal cell death. it is therefore suitable for the treatment of tinea, jock itch, ringworm, athlete's foot, tinea versicolor and paronychomycosis as well as the vaginal infection and secondary infection caused by the yeast (such as candida) and gram-positive bacteria. it is also effective in treating otitis externa and bacterial skin infections. 
 
the common adverse reactions and side effects of miconazole nitrate include: occasional allergy, blisters, burning feeling, redness, itching or other skin irritation. very rare angioedema, urticaria, eczema, contact dermatitis, erythema, pelvic pain (cramps), vaginal irritation, vaginal secretions and discomfort in the administration site. 
 
 
miconazole nitrate application:
 
miconazole is used to treat skin infections such as athlete's foot, jock itch, ringworm, and other fungal skin infections (candidiasis). this medication is also used to treat a skin condition known as pityriasis (tinea versicolor), a fungal infection that causes a lightening or darkening of the skin of the neck, chest, arms, or legs. miconazole is an azole antifungal that works by preventing the growth of fungus.

 

Details

name:miconazole nitrate 
cas:22832-87-7 
formula:c18h15cl4n3o4
molecular weight:479.16
synonyms:
nitric acid;conofite;1h-imidazole,1-[2-(2,4-dichlorophenyl)-2- [(2,4-dichlorophenyl)methoxy]ethyl]-,mononitrate;gyno-monistat;micatin;imidazole,mononitrate;florid,mononitrate;daktarin;aflorix;miconazol nitrate;
einecs:245-256-6
density:1.451g/cm3
melting point:170-185 °c
boiling point:555.1 °c at 760 mmhg
flash point:289.5 °ca
appearance:white crystal powder
assay: 98.5-101.5(%)
package: as per your requirement
storage: dry
application: antibiotic resistance to infection api.
 
 
miconazole nitrate description:
 
miconazole nitrate is a kind of antifungal agent which is the drug "dakelin" which we are familiar with as commonly used drugs for treating skin ringworm. it has various kinds of effects. it inhibit the biosynthesis of ergosterol which is the fungal cell membrane component, causing damage to the cell membrane structure, increasing the membrane permeability, resulting in the leakage of the intracellular components and inhibiting the glucose utilization, preventing the nutrient uptake, and finally leading to fungal cell death. it is therefore suitable for the treatment of tinea, jock itch, ringworm, athlete's foot, tinea versicolor and paronychomycosis as well as the vaginal infection and secondary infection caused by the yeast (such as candida) and gram-positive bacteria. it is also effective in treating otitis externa and bacterial skin infections. 
 
the common adverse reactions and side effects of miconazole nitrate include: occasional allergy, blisters, burning feeling, redness, itching or other skin irritation. very rare angioedema, urticaria, eczema, contact dermatitis, erythema, pelvic pain (cramps), vaginal irritation, vaginal secretions and discomfort in the administration site. 
 
 
miconazole nitrate application:
 
miconazole is used to treat skin infections such as athlete's foot, jock itch, ringworm, and other fungal skin infections (candidiasis). this medication is also used to treat a skin condition known as pityriasis (tinea versicolor), a fungal infection that causes a lightening or darkening of the skin of the neck, chest, arms, or legs. miconazole is an azole antifungal that works by preventing the growth of fungus.
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
how to order
 
1. let me know the products with quantity you are interesting and your requirement, you will get the best offer.
 
2. after we confirm all the details about the order, products will send out within 24 hours after we received your payment(moneygram,western union,t/t is accepted).
 
3. tracking no. will send to you within 2-3days.after 7days you will received your package.
 
4. we will take care of your order till parcel to your door, and expecting for your further feedback, 24 hours on line for after-sale service.
 
wuhan demeikai biotechnology co., ltd is a legitimate companies which registration in the trade and industry bureau.main business:research and development, production and sales of steriods,peptides,raw materials and intermediates.
the company has a legitimate import and export qualifications, and in the state ministry of commerce for the record registration, registration number 03027567.
 
we are the forefront of chinese for the production and sales of raw materials business, the company is located in wuhan university high-tech business incubator, relying on the "innovation" wave of national support program and having a reputation for goverment supporting plan.owning a large number of outstanding scientific research talents and equipped with advanced production equipment and efficiently sophisticated detection equipment, setting up a strict and scientific quality management system, and continuously committed to technological innovation, product innovation and management innovation.
 
company purpose:quality is the foundation of development,always maintain a competitive price.
hope to achieve mutually beneficial and win-win goal with our customers.
 
our superiority
1. we has passed the iso9001: 2000 (quality management system certification) iso14001: 2004 (environmental management system certification), ohsms (occupational health and safety system certification) three system certification, won the "attaches great importance to contract, keep promise" and won hubei province civilized units and many other honors. 
 
2.the company's large-scale, solid technical foundation, adequate supply,so that we can meet the different needs of various customers.
 
3. professional sales team to meet the various needs of customers, customers timely answers to various questions,achieve good communication,ensure good after-sales service and solve your worries.
 
4.improve the logistics system to ensure that customers will konw the movements of goods in the first time after the shipment.
 
5.to provide third-party product testing reports, integrity management.

 

 
laxogenin (5a-hydroxy) is an anabolic building block that is derived from plants, and it can be used by the body to create its own anabolics.  it does this by increasing protein synthesis and nitrogen retention, creating an anabolic environment in the body that gives the effects of increased muscle strength and mass, endurance, recovery, and lean gains.  what's more, laxogenin also inhibits cortisol - a nasty hormone we get from both mental and physical stress, which signals the body to store fat and burn muscle.
 
 
interestingly, people may not be aware that laxogenin was studied by the japanese as far back as the early 1960's, but it was not brought to the public attention until the 90's.  since then, supplement companies have used this compound in their products in order to give athletes a boost.
 
basic info of 5a-hydroxy laxogenin
product name: 5a-hydroxy laxogenin,spirostan-6-one, 3,5-dihydroxy-, (3b,5a,25r)-
synonyms: spirostan-6-one, 3,5-dihydroxy-, (3b,5a,25r)-;5a-hydroxy laxogenin
mf: c27h42o5
mw: 446.619
cas: 56786-63-1 
 
 
how 5a-hydroxy laxogenin works
 
laxogenin was isolated in 1992 from rhizomes of smilax sieboldii (a plant species found throughout the world, but native to asia).  it is considered to be a type of steroidal sapogenin, and part of a group called brassinosteroids, which are part of a group of 40 different steroids that are synthesized from species of plants.   within the plant, these amazing compounds promote growth and vitality.
 
smilax sieboldii seeds
fig 2. smilax sieboldii seeds
however, a study from the faseb journal in 2010 showed that these brassinosteroids actually trigger anabolic effects by increasing protein synthesis, while halting protein breakdown.  as we all know, protein is the building block of muscle, but with laxogenin you also get such benefits as fat loss and performance enhancement.
 
as a matter of fact, laxogenin is known to be the only product available that can give you anabolic gains in mass and strength without the steroidal suppression, or other side effects.  therefore, athletes can use it on a caloric restricted diet to prevent loss of muscle and strength.  furthermore,  it will also help control glucose and increase thyroid function (metabolism).  besides, according to one experiment from the late 80's in japan, laxogenin has been shown to have anti inflammatory benefits and a prominent anti-tumor potential.
 
5a-hydroxy laxogenin benefits
 
the benefits of laxogenin are not as strong as anabolic steroids, but they do have some advantages:
 
it will not show up on any narcotic, or anabolic, drug screens.  tested athletes need not worry about being busted for this compound.
it has no effects on the hpta (hypothalamus-pituitary-testicular axis) or estrogen levels, so it is not necessary to run a post cycle therapy (pct) or use an aromatase inhibitor.  meanwhile, anabolic steroids cause lh (luteinizing hormone) suppression of about 95%, and require a strong pct for a proper recovery.
results can be very fast with laxogenin, unlike some injectable steroids, which take time to give any considerable results.
just like anabolic androgenic steroids, laxogenin also inhibits cortisol without other side effects.  hence, it can prevent fat gain.
this compound increases protein synthesis by over 200%, giving you the advantages of steroid use, without the harsh side effects found with steroids.
it does not cause liver strain like oral anabolic steroids or pro-hormones do.
laxogenin does not cause increases in dht, which can fry your head hair follicles.  thus, your hairline will stay intact.
 

 

dutasteride basic info.
cas: 164656-23-9
assay: 99%
packing: 25kg/drum
mf: c27h30f6n2o2
mw: 528.53
appearance: white to light yellow crystalline powder
 
dutasteride applications :
dutasteride (brand name avodart), it is used to treat benign prostatic hyperplasia. it increases the risk of erectile dysfunction and decreased sexual desire.
avodart (dutasteride) 500 µg soft capsules
dutasteride is useful for treating benign prostatic hyperplasia (bph); colloquially known as an "enlarged prostate"
 
dutasteride, with the iupac name of (1s,3as,3bs,5ar,9ar,11as)-n-[2,5-bis(trifluoromethyl)phenyl]-9a,11a-dimethyl-7-oxo-1,2,3,3a,3b,4,5,5a,6,9b,10,11-dodecahydroindeno[5,4-f]quinoline-1-carboxamide, is one kind of white crystalline solid. this chemical belongs to the product categories which include miscellaneous biochemicals; all inhibitors; inhibitors; intermediates & fine chemicals; pharmaceuticals; steroids.
 
 
uses of dutasteride: dutasteride can inhibits the conversion of testosterone into dihydrotestosterone (dht). it is approved for the treatment of benign prostatic hyperplasia (bph), besides it is prescibed off-label for the treatment of male pattern baldness (mpb).
********************************
dutasteride is used for:
 
treating symptoms of benign prostatic hyperplasia (bph) or enlargement of the prostate gland. it also helps to reduce the risk of urinary blockage and the need for surgery to treat bph. it may be used alone or along with another medicine (tamsulosin).
 
dutasteride is a 5 alpha-reductase enzyme inhibitor. it works by lowering levels of a hormone called dihydrotestosterone (dht), which is a major cause of prostate growth. lowering dht leads to shrinkage of the enlarged prostate gland.
a man’s prostate continues to grow throughout his lifetime. for some men, their prostate becomes so large that it begins to cause problems. this is a condition called benign prostatic hyperplasia (bph). bph is more commonly know as enlarged prostate. this condition typically develops in older men. men with bph may have symptoms such as the need to urinate more often, difficulty starting a urine stream, or decreased urine flow.
 
drugs that treat bph belong to a class called 5alpha-reductase inhibitors. dutasteride and finasteride are two popular 5alpha-reductase inhibitors that are used to treat bph. these drugs prevent male hormones from increasing the size of your prostate. you generally need to have been taking one of these drugs for at least 6 months before your bph symptoms improve.
 

 

name: tetracaine 
other name:amethocalne,dlcalne,pontocaine,pantocaine,decicaine
cas no.:94-24-6
mf: c15h24n2o2
mw: 264.36
einecs: 202-316-6
storage temp. 2-8°c
purity: 99%
description : white crystal or crystalline powder
package: 1kg foil bag; 25kg drum
 
description:
 
tetracaine (also known as amethocaine; trade name pontocaine and dicaine) is a potent local anesthetic of the ester group. it is mainly used topically in ophthalmology and as an antipruritic, and it has been used in spinal anesthesia.
 
how it works:
 
topical anesthetics stabilize the neuronal membrane and prevent the initiation and transmission of nerve impulses, thereby effecting local anesthesia. the onset of anesthesia usually begins within 30 seconds and lasts a relatively short period of time.
 
application:
tetracaine is a topical opththalmic anesthetic used to relieve the pain the skin and as an eye drops for minor eye operations. it prevents voltage-sensitive release of ca2+ from sarcoplasmic reticulum and can be used as a spinal anesthetic.
 
tetracaine is a local anesthetic (numbing medicine). it works by blocking nerve signals in your body.
 
tetracaine topical (for the skin) is used to numb different parts of the body before a medical test or procedure.
 
tetracaine topical may also be used for purposes not listed in this medication guide.
 

 

idarubicin basic info.
 
product name: idarubicin hydrochloride
synonyms: idarubicin hcl;idarubicin hydrochloride;4-demethoxy-daunomycihydrochloride;4-demethoxydaunorubicinhydrochloride;(7s-cis)-9-acetyl-7-[(3-amino-2,3,6-trideoxy-α-l-lyxo-hexopyranosyl)oxy]-7,8,9,10-tetrahydro-6,9,11-trihydroxy-5,12-naphthacenedione;4-dmd hcl;5,12-naphthacenedione, 9-acetyl-7-[(3-amino-2,3,6-trideoxy-α-l-lyxo-hexopyranosyl)oxy]-7,8,9,10-tetrahydro-6,9,11-trihydroxy-, hydrochloride, (7s,9s)-;5,12-naphthacenedione, 9-acetyl-7-[(3-amino-2,3,6-trideoxy-α-l-lyxo-hexopyranosyl)oxy]-7,8,9,10-tetrahydro-6,9,11-trihydroxy-, hydrochloride, (7s-cis)-
cas: 57852-57-0
mf: c26h28clno9
mw: 533.95
einecs: 260-990-7
product categories: api;drug analogues;intermediates & fine chemicals;pharmaceuticals;idamycin, zavedos, 4-demethoxydaunorubicin;anti-cancer&immunity
mol file: 57852-57-0.mol
idarubicin hydrochloride structure
idarubicin hydrochloride chemical properties
mp: 183-185 c
storage temp.: 2-8°c
safety information
hazard codes: t+,xn
risk statements: 60-61-28-40
safety statements: 53-45-36-22
ridadr: un 2811
rtecs: hb7877000
msds information
idarubicin hydrochloride usage and synthesis
chemical properties: orange solid
 
idarubicin is used for:
treating a certain type of cancer (acute myeloid leukemia [aml]). it may also be used for other conditions as determined by your doctor.
idarubicin is a cytotoxic agent. it works by inhibiting activities of the cancer cell necessary for life and growth. this prevents the cancer cell from reproducing and results in death of the cancer cell.
 

 

maytansine basic info.
product name:maytansine
cas:35846-53-8
molecular formula:c34h46cln3o10
formula weight:692.201
description:maytansine (usan), or maitansine (inn), is a cytotoxic agent. it inhibits the assembly of microtubules by binding to tubulin at the rhizoxin binding site.
it is a macrolide of the ansamycin type and can be isolated from plants of the genus maytenus.
 

 

pf06463922 basic info.
 
synonyms: (10r)-7-amino-12-fluoro-10,15,16,17-tetrahydro-2,10,16-trimethyl-15-oxo-2h-4,8-methenopyrazolo[4,3-h][2,5,11]benzoxadiazacyclotetradecine-3-carbonitrile
 
cas:1454846-35-5, 
mf:c21h19fn6o2
mw:406.41
pf-06463922 is a novel, orally available, cns-penetrant, atp-competitive inhibitor of alk/ros1 with ki of <0.02 nm, <0.07 nm, and 0.7 nm for ros1, alk (wt), and alk (l1196m), respectively.
usage:pf-06463922 demonstrates significant cell activity against alk and a large set of alk clinical mutations with ic50 ranging from 0.2 nm-77 nm. pf-06463922 exhibited subnanomolar cellular potency against oncogenic ros1 fusions and inhibited the crizotinib-refractory ros1(g2032r) mutation and the ros1(g2026m) gatekeeper mutation. compared with crizotinib and the second-generation alk/ros1 inhibitors ceritinib and alectinib, pf-06463922 showed significantly improved inhibitory activity against ros1 kinase. in vivo: pf-06463922 showed marked antitumor activity in tumor models expressing fig-ros1, cd74-ros1, and the cd74-ros1(g2032r) mutation. furthermore, pf-06463922 demonstrated antitumor activity in a genetically engineered mouse model of fig-ros1 glioblastoma.
 
pf-06463922 application:
 
 pf-06463922 is the second generation of crizotinib,in total alk inhibitors divided into the third generation.
 the alk drug programs is crizotinib→ap26113,ch5424802,ldk378→pf06463922。
 
 the efficacy of pf-06463922 is crizotinib forty times,ap26113 six times.
 pf-06463922 can inhibit 9 mutation after resistant of crizotinib,ap26113 can inhibit two kinds,ch5424802  can inhibit three kinds,ldk378can inhibit four kinds,but ap26113 and ldk378 just like sister,as they have almost the same structure, mechanism of action.
 
 3922 using new big ring structure, action mechanism and the effect is greatly increased.
 
  pf-06463922 also can inhibition of ros1 targets.its force is 3 times of alk, is currently ros1 second generation of medicine.
 

 

trenbolone acetate basic info
product name: revalor-h, trenbolone acetate, trenbolone acetate, trenbolone acetate; finaplix; finaplix; finaplix-h
synonyms: finaplix; ru1697; trienboloneacetate; revalor-h
cas: 10161-34-9
mf: c20h24o3
mw: 312.4
einecs: 233-432-5
appearance: pale yellow solid
usage: a steroid used to increase the muscle growth of livestock. 
standard: usp
purity: 99%min
min order: 10g
 
 
trenbolone acetate's application on bodybuilding 
 
trenbolone acetate is very fast acting. therefore, bodybuilders choosing to use this substance often find  that daily injections are best for keep blood levels as consistent as possible.simply put . trenbolone acetate is the most powerful overall steroid in use by bodybuilders today. tren, as it is often called, is both highly androgenic and anabolic. it is chemically unable to aromatize, and therefore produces no estrogen buildup. this, along with its high androgenic properties, makes the muscle produced by this drug very hard and defined. 
 
tren acetate can be used as pharmaceutical material. its main function is to promote metabolism. anabolic effects include growth of muscle mass and strength, increased bone density and strength, and stimulation of linear growth and bone maturation. 
 
tren acetate is the most anabolic of all the non-estrogenic commercial steroids, with muscle-building properties often compared to test and dianabol but without the same level of water retention and without estrogen conversion.
 
trenbolone acetate dosage:
trenbolone acetate is usually used at doses of 35-150 mg/day, and more typically 50-100 mg/day. masteron is a good choice for this purpose.
 
as for the higher 150 mg/figure, this generally is used for the purpose of increased nervous system stimulation compared to 100 mg/day rather than for further mass or strength improvements, which are already maximized or very nearly maximized at 100 mg/day.
 
most users find 50-75 mg/day to be an ideal dosage range, giving excellent benefit as part of an anabolic steroid stack. 
 

 

trenbolone hexahydrobenzyl carbonate basic info.
fw:c26h34o4
mw:410.55
cas:23454-33-3
synonyms:estra-4,9,11-trien-3-one,cyclohexylmethylcarbonate (8ci);carbonic acid, cyclohexylmethyl ester, ester with 17b-hydroxyestra-4,9,11-trien-3-one(8ci);cyclohexanemethanol, hydrogen carbonate,ru 2580;trenbolonehexahydrobenzyl carbonate;
einecs:245-669-1
density:1.17 g/cm3
boiling point:607.9 °c at 760 mmhg
flash point:261.7 °c
appearance:light yellow powder
assay: above 99%
package: 1kg/aluminum bags
storage: keep away from fire and heat source
application: for research
 
parabolan is trenbolone cyclohexylmethylcarbonate. the half-life of a steroid ester is mostly dependent on its ratio of fat solubility to water solubility: the longer chain the ester, the higher this ratio, and the longer the half-life. this particular carbonate could be most closely compared with an enanthate ester; the half-life is probably a little less than week.  
 
trenbolone cyclohexylmethylcarbonate function:
protein assimilation hormonal. trenbolone is a steroid used by veterinarians on livestock to increase muscle growth and appetite, to increase the half-time, trenbolone is not used in an unrefined form, but is rather administered as ester derivatives such as trenbolone acetate, trenbolone enanthate ortrenbolone cyclohexylmethylcarbonate, a normal bodybuilding dosage can range from 200mg/week to 1400mg/ week. trenbolone acetate can be injected once a week, also trenbolone acetate is often refined to as "fina" by user, trenbolone compounds have a binding affinity for the androgen receptor five times as high as that of testosterone.  
 

 

cjc-1295 dac and cjc-1295 (also known as modified grf 1-29) are both releasing hormones (ghrh). their action in the human body is identical but the difference between the two peptides are the span of the half-life. modified grf 1-29 and sermorelin have a very short acting half-life of about 30 minutes, while cjc-1295 dac has a half-life that can last up to approximately 8 days. many a scientist have reported that the short half-life of sermorelin and modified grf 1-29 is considered to be much more natural as they produce a short pulse of human.
 
cjc-1295 with dac basic info.
product description: cjc-1295 2mg/vial
type: immune function agentsgrade
standard: medicine grade
classification: brassinosteroid
cas: 63288-34-0 
mf: c165h271n47o46
molecular weight: 3649.30
purity (hplc): 98.0%
appearance: white powder
single impurity(hplc): 1.0%
amino acid composition: 10% of theoretical
peptide content(n%): 80%(by %n)
water content(karl fischer): 6.0%
acetate content(hpic): 15.0%
mass balance: 95.0~105.0%
 
 
cjc-1295 with dac usage:
cjc1295 dac has shown some amazing results as a hormone releasing hormone (ghrh) analog. not onlyhas cjc1295 shown the ability to increase hormone and secretion and its benefits, but it has been able to do so in very large amounts. recent research studies have shown that cjc - 1295 stimulates gh and secretion, and will keep a steady increase with no increase in prolactin, leading to intense fat loss, and increases protein synthesis. cjc-1295 dac is a long acting hormone releasing hormone, which causes the anterior pituitary to release more hormone.  the objective of the peptide was to treat visceral fat deposits in obese aids patients, as increased levels of exogenous are presumed to increase lipolysis (fat loss). the clinical research was ultimately successful for most research subjects. ghrelin, released from the gut, which circulates and acts as a hunger hormone, has synergistic activity in the body with ghrh and also suppresses somatostatin to make way for the ghrh pulse. an example of a ghrp (gh releasing peptide) is hexarelin or ghrp2. cjc 1295 dac is a exceptionally designed peptide and is known for being the finest of the  secretogues.
 

 

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