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221231-10-3

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221231-10-3 Usage

Description

AOD 9604 is a peptide fragment (Fragment 177-191) of the C-terminus of Human Growth Hormone, with a tyrosine added at the N-terminal end. It is also known as "Anti-Obesity Drug" and has an amino acid sequence that resembles the lipolytic region of human growth hormone, which is believed to be responsible for fat burning. AOD 9604 has been promoted as a weight loss supplement, a muscle and cartilage repair aid, and a treatment for osteoarthritis.

Uses

Used in Weight Loss Applications:
AOD 9604 is used as a weight loss supplement for its ability to mimic the lipolytic region of human growth hormone, promoting fat burning and reducing body fat in the mid-abdominal area. It has been shown to be effective in obese, overweight, and average-built individuals.
Used in Muscle and Cartilage Repair:
AOD 9604 is used as an aid for muscle and cartilage repair due to its structural similarity to the human growth hormone, which is known to play a role in tissue repair and regeneration.
Used in Osteoarthritis Treatment:
AOD 9604 is used as a treatment for osteoarthritis, potentially due to its ability to support tissue repair and regeneration, as well as its anti-inflammatory properties.
Note: The provided materials do not mention any specific industries for the applications. However, the applications mentioned are generally applicable across various health and wellness industries, including pharmaceuticals, dietary supplements, and sports medicine.

How it works

AOD-9604, also known as Tyr-hGH Frag 176-191 has been proven to have a strong fat burning capacity, without creating a desire to overeat. It doesn't affect blood sugar or tissue growth. (Heffernan 2001 Heffernan 2001, Ng 2000). AOD-9604 activates degradation and fat burning (oxidation), by a method that doesn't use hGH receptor. It has its own mechanism of action independent of hGH. Studies on rodents, pigs, dogs & humans have identified AOD-9604 mechanism where it triggers fat release from the obese fat cells predominantly and works to reduce the accumulation of new fat in fat cells as well as increasing fat burning. What is extraordinary about the AOD-9604 is its ability to reduce abdominal fat stores. The second most potent fat loss peptide is CJC-1295, since it leads to the increase in overall GH levels in the body (the opposite of what happens typically as individual age) This explains one of the reasons people have tended to gain fat as they get older. If your only goal is fat loss, it's usually best to avoid using products GHRP (GHRP-6, GHRP-2 or GHRH’s) because they may give you the side effects of increased hunger and raised cortisol. AOD-9604 does not increase hunger or raise cortisol.

Benefits

Reduces Body FatTriggers fat release from obese fat cells predominantly more than lean onesMimics the way natural growth hormone regulates fat metabolismNo adverse effects on blood sugar or growthAOD-9604 stimulates lipolysisInhibits lipogenesis that's the transformation of non-fatty foods into body fatAOD 9604 has been shown to have very favorable cartilage repair and regenerative properties, especially when paired with peptide BPC 157.

Health Effects

In addition to its fat loss properties, studies show that this peptide can also treat osteoarthritis, as well as promote bone and cartilage repair.Research in rats shows that AOD9604 injections directly into arthritic joints can help improve pain, quality of life, and lessen disability. The clinical exams indicate that AOD 9604 therapy is effective in reducing joint dysfunction and may work as a preventative as well as a treatment.There's also evidence to suggest that AOD-9604 can directly reduce the risk of heart disease. Though fat reduction plays a role, scientists believe it is also due to the way this peptide affects the metabolism.Clearly, the research on AOD 9604 is fascinating and looks highly promising to be an available drug in years to come. Thanks to its minimal side effects, scientists believe this to be the weight loss drug of the future.

Check Digit Verification of cas no

The CAS Registry Mumber 221231-10-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,1,2,3 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 221231-10:
(8*2)+(7*2)+(6*1)+(5*2)+(4*3)+(3*1)+(2*1)+(1*0)=63
63 % 10 = 3
So 221231-10-3 is a valid CAS Registry Number.

221231-10-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name AOD-9604

1.2 Other means of identification

Product number -
Other names AOD 9604

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:221231-10-3 SDS

221231-10-3Synthetic route

C81H130N24O24S2

C81H130N24O24S2

AOD-9604
221231-10-3

AOD-9604

Conditions
ConditionsYield
Stage #1: C81H130N24O24S2 With iodine In acetic acid at 20℃;
Stage #2: With isoascorbic acid In acetic acid
H-Tyr-Leu-Arg-Ile-Val-Gln-Cys-Arg-Ser-Val-Glu-Gly-Ser-Cys-Gly-Phe-OH
855516-60-8

H-Tyr-Leu-Arg-Ile-Val-Gln-Cys-Arg-Ser-Val-Glu-Gly-Ser-Cys-Gly-Phe-OH

AOD-9604
221231-10-3

AOD-9604

Conditions
ConditionsYield
With air for 15h; pH=8;

221231-10-3Downstream Products

221231-10-3Relevant articles and documents

One-Pot Peptide Ligation-Oxidative Cyclization Protocol for the Preparation of Short-/Medium-Size Disulfide Cyclopeptides

Spengler, Jan,Blanco-Canosa, Juan B.,Forni, Luciano,Albericio, Fernando

supporting information, p. 4306 - 4309 (2018/07/29)

Native chemical ligation (NCL) employing the N-methylbenzimidazolinone (MeNbz) linker readily provided the linear precursor of a 16-mer peptide that is difficult to obtain by stepwise solid-phase peptide synthesis. NCL and the workup conditions were improved toward a protocol that allows for quantitative removal of the 4-hydroxymercaptophenol additive and subsequent formation of the disulfide bridge in the NCL cocktail by oxidation in air, tolerated by the presence of tris(hydroxypropyl)phosphine.

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