Almestrone

TargetMol
Product Code: TAR-T29886
Supplier: TargetMol
CodeSizePrice
TAR-T29886-5mg5mg£850.00
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Quantity:
Prices exclude any Taxes / VAT

Overview

Regulatory Status: RUO
Shipping:
cool pack
Storage:
-20℃

Images

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Further Information

Bioactivity:
Almestrone (developmental code names Ba 38372, Ciba 38372), also known as 7α-methylestrone, is a synthetic, steroidal estrogen which was synthesized in 1967 but was never marketed. It is used as a precursor in the synthesis of several highly active steroids.
CAS:
10448-96-1
Formula:
C19H24O2
Molecular Weight:
284.399
Purity:
0.98
SMILES:
[H][C@@]12CCC(=O)[C@@]1(C)CC[C@]1([H])c3ccc(O)cc3C[C@@H](C)[C@@]21[H]

References

1. Geranmayeh F, Brownsett SL, Wise RJ. Task-induced brain activity in aphasic stroke patients: what is driving recovery? Brain. 2014 Jun 28. pii: awu163. [Epub ahead of print] Review. PubMed PMID: 24974382. 2. Price KA, Tinker AM. Creativity in later life. Maturitas. 2014 Jun 7. pii: S0378-5122(14)00194-7. doi: 10.1016/j.maturitas.2014.05.025. [Epub ahead of print] Review. PubMed PMID: 24974278. 3. Fakurnejad S, Scheer JK, Patwardhan AG, Havey RM, Voronov LI, Smith ZA. Biomechanics of thoracolumbar burst fractures: Methods of induction and treatments. J Clin Neurosci. 2014 Jun 25. pii: S0967-5868(14)00249-5. doi: 10.1016/j.jocn.2014.05.002. [Epub ahead of print] Review. PubMed PMID: 24974189. 4. Lalloo C, Stinson JN. Assessment and treatment of pain in children and adolescents. Best Pract Res Clin Rheumatol. 2014 Apr;28(2):315-330. doi: 10.1016/j.berh.2014.05.003. Review. PubMed PMID: 24974065.