China (Mainland)
Cyclopenta[5,6]naphth[1,2-f]indazol-1-ol, 1,2,3,3a,3b,4,5,5a,6,7,10,10a,10b,11,12,12a-hexadecahydro-1,10a,12a-trimethyl- CAS NO.10418-03-8
- FOB Price: USD: 1.00-1.00 /Gram Get Latest Price
- Min.Order: 1 Gram
- Payment Terms: D/P,T/T,Other
- Available Specifications:
top(1-10)Gram
- Product Details
Keywords
- tevabolin;anabol;stromba;estazol
- favourable price of stanazol
- Bodybuilding Sports Nutrition Supplement
Quick Details
- ProName: Cyclopenta[5,6]naphth[1,2-f]indazol-1-...
- CasNo: 10418-03-8
- Molecular Formula: C21H32N2O
- Appearance: white crystalline powder
- Application: For research purposes only
- DeliveryTime: One day
- PackAge: apis or finished product
- Port: Shenzhen、Guangzhou、Shanghai、HK
- ProductionCapacity: 100 Kilogram/Day
- Purity: 99.8%
- Storage: cryo drying
- Transportation: shipping by EMS,DHL,TNT,FEDEX,UPS or a...
- LimitNum: 1 Gram
- Moisture Content: 0%
- Impurity: 0%
Superiority
Medical uses
Stanozolol has been used with some success in treated venous insufficiency. It stimulates blood fibrinolysis and has been evaluated for the treatment of the more advanced skin changes in venous disease such as lipodermatosclerosis. Several randomized trials noted improvement in the area of lipodermatosclerosis, reduced skin thickness, and possibly faster ulcer healing rates with stanozolol. It has also been used to successfully treat hereditary angioedema.
Non-medical uses
Stanozolol is used for physique- and performance-enhancing purposes by competitive athletes, bodybuilders, and powerlifters.
Side effects
See also: Anabolic steroid § Adverse effects
See also: Anabolic steroid § Adverse effects
Side effects of stanozolol include virilization (masculinization), hepatotoxicity, and others.
Pharmacology
Pharmacodynamics
As an AAS, stanozolol is an agonist of the androgen receptor (AR), similarly to androgens like testosterone and DHT. Its affinity for the androgen receptor is about 22% of that of dihydrotestosterone. Stanozolol is not a substrate for 5α-reductase as it is already 5α-reduced, and so is not potentiated in so-called "androgenic" tissues like the skin, hair follicles, and prostate gland. This results in a greater ratio of anabolic to androgenic activity compared to testosterone. In addition, due to its 5α-reduced nature, stanozolol is non-aromatizable, and hence has no propensity for producing estrogenic effects such as gynecomastia or fluid retention. Stanozolol also does not possess any progestogenic activity of significance. Because of the presence of its 17α-methyl group, the metabolism of stanozolol is sterically hindered, resulting in it being orally active, although also hepatotoxic.
As an AAS, stanozolol is an agonist of the androgen receptor (AR), similarly to androgens like testosterone and DHT. Its affinity for the androgen receptor is about 22% of that of dihydrotestosterone. Stanozolol is not a substrate for 5α-reductase as it is already 5α-reduced, and so is not potentiated in so-called "androgenic" tissues like the skin, hair follicles, and prostate gland. This results in a greater ratio of anabolic to androgenic activity compared to testosterone. In addition, due to its 5α-reduced nature, stanozolol is non-aromatizable, and hence has no propensity for producing estrogenic effects such as gynecomastia or fluid retention. Stanozolol also does not possess any progestogenic activity of significance. Because of the presence of its 17α-methyl group, the metabolism of stanozolol is sterically hindered, resulting in it being orally active, although also hepatotoxic.
Pharmacokinetics
Stanozolol has high oral bioavailability, due to the presence of its C17α alkyl group and the resistance to gastrointestinal and liver metabolism that it results in. The medication has very low affinityfor human serum sex hormone-binding globulin (SHBG), about 5% of that of testosterone and 1% of that of DHT. Stanozolol is metabolized in the liver, ultimately becoming glucuronide and sulfateconjugates. Its biological half-life is reported to be 9 hours when taken by mouth and 24 hours when given by intramuscular injection in the form of an aqueous suspension.It is said to have a duration of action of one week or more via intramuscular injection.
Stanozolol has high oral bioavailability, due to the presence of its C17α alkyl group and the resistance to gastrointestinal and liver metabolism that it results in. The medication has very low affinityfor human serum sex hormone-binding globulin (SHBG), about 5% of that of testosterone and 1% of that of DHT. Stanozolol is metabolized in the liver, ultimately becoming glucuronide and sulfateconjugates. Its biological half-life is reported to be 9 hours when taken by mouth and 24 hours when given by intramuscular injection in the form of an aqueous suspension.It is said to have a duration of action of one week or more via intramuscular injection.
Details
FAQ
1. Can I get a free sample
1. Can I get a free sample
Yes, but you have to pay the courier fee.
2. How to pay
We accept payments in the form of , MoneyGram, Bitcoin, etc.
3. What should I do if we don’t ship after payment
We are a formal company certified by LOOKCHEM Integrity, you can provide proof of payment to LOOKCHEM complaints.
4. How long after the payment can be shipped
We have stocked products that are shipped within 24 hours. If you need to customize the product, we will negotiate the delivery cycle.
5. How is the safety of transportation
We will choose the safest delivery method to ensure customs clearance and safety during transportation.
6. What kind of company is THETA BIO
In 2009, Dr Zhang Lin from Johns Hopkins University founded the theta Biological Laboratory. He is committed to the study of protein assimilation preparations.
In 2013,Dr Zhang Lin returned to China to work in MSD China, and continued to work on biopharmaceutical research and development.
In 2018,Dr Zhang Lin founded shaoyang Theta Biological Thechnology Co.,Ltd.
Business Scope:
Pharmaceutical intermediate
Biotechology development
Fine organic chemistry
Biopharmaceutical
History of the company
In 2009,Dr Zhang Lin from Johns Hopkins University founded the theta Biological Laboratory.He is committed to the study of protein assimilation preparations.
In 2013,Dr Zhang Lin returned to China to work in MSD China,and continued to work on biopharmaceutical research and development.
In 2018,Dr Zhang Lin founded shaoyang Theta Biological Thechnology Co.,Ltd.
Business Scope:
Pharmaceutical intermediate
Biotechology development
Fine organic chemistry
Biopharmaceutical
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