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Home > Products >  MK-677 Ibutamoren SARMs

MK-677 Ibutamoren SARMs CAS NO.159752-10-0

  • FOB Price: USD: 60.00-60.00 /Gram Get Latest Price
  • Min.Order: 1 Gram
  • Payment Terms: T/T,Other
  • Available Specifications:

    99%(1-3)Gram

  • Product Details

Keywords

  • MK-677
  • Ibutamoren
  • mesylate

Quick Details

  • ProName: MK-677 Ibutamoren SARMs
  • CasNo: 159752-10-0
  • Molecular Formula: C28H40N4O8S2
  • Appearance: Freeze dry powder
  • Application: Lost weight, muscle growth
  • DeliveryTime: 3 days
  • PackAge: Safe Packing as your requirement
  • Port: Hong Kong
  • ProductionCapacity: 1 Kilogram/Day
  • Purity: 99.5%
  • Storage: ambiant temperature storage
  • LimitNum: 1 Gram
  • Moisture Content: 0
  • Impurity: 0

Superiority

  • much less expensive
  • Europe storage

1.Rich experience

We specialize in this filed for many years,our steriods and hormones exported to all over the world and established long friendly relations of coroperation with them.

2.Great quality,purity and favorable

Good quality is one of our biggest secert to success;u can get the best quality and service from us.

3.Safest and fastest delivery

We have adequate stock so that we can deliver the products with 24 hours as soon as receiving the payment.Fast and discreet shipment will be arranged to pass customs.

4.Good package

Unique ways to ship 10g to 100kg powders to your destination.We offer melting powder into liquid service and ship the liquid in special bottles.

5.Great after-sales service

Any questions or problems after receiving the product,pls feel free to contact us.Problems would be solved immediately.

 

Details

Name   Ibutamoren mesylate
Synonyms   MK-677; 2-Amino-N-[(1R)-2-[1,2-dihydro-1-(methylsulfonyl)spiro[3H-indole-3,4'-piperidin]-1'-yl]-2-oxo-1-[(phenylmethoxy)methyl]ethyl]-2-methylpropanamide methanesulfonate
 
Molecular Structure    
 
Molecular Formula   C27H36N4O5S.CH4O3S
Molecular Weight   624.77
CAS Registry Number   159752-10-0
 
 
SARMS
Name CAS NO.
Ostarine,MK-2866, Enobosarm 841205-47-8 
Andarine (S-4) 401900-40-1
MK-677, Ibutamoren,mesylate 159752-10-0 
LGD-4033 1165910-22-4 
GW-501516/Cardarine 317318-70-0 
AICAR 2627-69-2
SR9009 137986-29-9
RAD-140 118237-47-0
Flibanserin 167933-07-5
Carphedon 77472-70-9 
Coluracetam 135463-81-9 
Sunifiram 314728-85-3
Adrafinil 63547-13-7
Pirfenidone 53179-13-8
YK11 1370003-76-1
　 　
 
 

1.Description

Ibutamoren mesylate (MK-0677) is an orally active nonpeptide growth hormone (GH) secretagogue.
IC50 Value:
Target: GHSR
Ibutamoren mesylate (MK-0677) stimulates GH release through a pituitary and hypothalamic receptor that is different from the GH-releasing hormone receptor. MK-677is a drug which acts as a potent, orally active growth hormone secretagogue, mimicking the GH stimulating action of the endogenous hormone ghrelin. It has been demonstrated to increase the release of, and produces sustained increases in plasma levels of several hormones including growth hormone and IGF-1, but without affecting cortisol levels. It is currently under development as a potential treatment for reduced levels of these hormones, such as in growth hormone deficient children or elderly adults, and human studies have shown it to increase both muscle mass and bone mineral density, making it a promising therapy for the treatment of frailty in the elderly. Ibutamoren mesylate (MK-0677) also alters metabolism of body fat and so may have application in the treatment of obesity.


2 . Application area


An experimental drug meant to control lipids and increase the level of HDL, or good cholesterol, in the bloodstream. A cell-permeable, thiazolyl compound that acts as a potent, high affinity, PPARd agonist. Exhibits selectivity for PPARd compared t 
Usage An experimental drug meant to control lipids and increase the level of HDL, or good cholesterol, in the bloodstream. A cell-permeable, thiazolyl compound that acts as a potent, high affinity, PPARδ agonist. Exhibits selectivity for PPARδ compared to PPARα and PPARγ. Does not exibit any activity against other nuclear or non-nuclear receptors. Reported to increase cholesterol efflux and ABAC1 expression in macrophages, fibroblasts, and intestinal cells. 


3 . Specification:



TEST		 ACCEPTANCE CRITERLA RESULTS
  TLC Positive
Identification UV spectrum Positive
  IR spectrum Positive
Characteristics White to yellowish-white crystalline powder conform
Melting point 32 ~ 37ºC 33~36ºC
Specific optical rotation +77°~+82° +79.3°
Loss on drying ≤0.5% 0.15%
Assay 97 ~ 103% 99.08%
Free heptanoic acid ≤0.2 % 0.10%
Related substances ≤2% Pass
  Acetone ≤100ppm Pass
Residual solvents(GC) Methanol ≤100ppm Pass
  Pyridine ≤100ppm Pass
Particle size   Pass
 
Polypeptide
NO. Name specification
T-A001 MGF 2mg
T-A002 PEG MGF 2mg
T-A003 CJC-1295 with DAC 2mg
T-A004 CJC-1295 without DAC 2mg
T-A005 PT-141 10mg
T-A006 MT-1 10mg
T-A007 MT-2 10mg
T-A008 GHRP-2 5mg
T-A008 GHRP-2 10mg
T-A009 GHRP-6 5mg
T-A009 GHRP-6 10mg
T-A010 Ipamorelin 2mg
T-A011 Hexarelin 2mg
T-A012 Sermorelin 2mg
T-A013 Oxytocin 2mg
T-A014 TB500 2mg
T-A015 pentadecapeptide BPC 157 2mg
T-A016 HGH 176-191 2mg
T-A017 Triptorelin 2mg
T-A018 Tesamorelin 2mg
T-A020 Gonadorelin 2mg
T-A020 Gonadorelin 10mg
T-A021 DSIP  2mg
T-A022 Selank 5mg
　 　 　
　 　 　
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