| Company Name: |
Energy Chemical
|
| Tel: |
021-58432009 400-005-6266 |
| Email: |
marketing@energy-chemical.com |
| Products Intro: |
Product Name:Topterone
CAS:60607-35-4
Purity:NULL Package:100mg;10mg;25mg;50mg Remarks:NULL
|
| Company Name: |
TargetMol Chemicals Inc.
|
| Tel: |
15002134094 |
| Email: |
marketing@targetmol.cn |
| Products Intro: |
Product Name:Topterone
CAS:60607-35-4
Purity:100.00% Package:5mg/RMB 12600;1mg/RMB 4900
|
topterone manufacturers
- Topterone
-
- $1800.00
-
2026-05-11
- CAS:60607-35-4
- Purity: 100.00%
- Supply Ability: 10g
- Topterone
-
- $1800.00
-
2025-08-22
- CAS:60607-35-4
- Purity: 100.00%
- Supply Ability: 10g
|
| | topterone Basic information |
| Product Name: | topterone | | Synonyms: | topterone;17β-Hydroxy-17-propylandrost-4-en-3-one;Win-17665;Androst-4-en-3-one, 17-hydroxy-17-propyl-, (17β)- | | CAS: | 60607-35-4 | | MF: | C22H34O2 | | MW: | 330.509 | | EINECS: | 2623214 | | Product Categories: | | | Mol File: | 60607-35-4.mol |  |
| | topterone Chemical Properties |
| Melting point | 114.6-116.0 °C(Solv: benzene (71-43-2); hexane (110-54-3)) | | Boiling point | 459.8±45.0 °C(Predicted) | | density | 1.08±0.1 g/cm3(Predicted) | | pka | 15.13±0.60(Predicted) |
| | topterone Usage And Synthesis |
| Uses | Topterone functions as steroidal antiandrogen drug. Also, the are used in acne and androgenic alopecia treatment. | | in vivo | Topterone, is administered parenterally or topically to rats, rabbits or hamsters to determine its endocrine profile. Systemic administration demonstrates that Topterone is both antiandrogenic and progestational. Topical application fails to elicit a systemic antiandrogenic response at 1 g/kg/day and only a minimal progestational response is seen at 32 mg/kg/day. No other endocrine activities are detected[1]. Topterone inhibits stimulation of flank organ development of castrated immature male hamsters by both testosterone and dihydrotestosterone, whereas Progesterone inhibits the stimulation by only testosterone. Topical application of Topterone, has been shown to cause a regression in the development of the flank organ[2]. |
| | topterone Preparation Products And Raw materials |
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