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4416-57-3,MFCD00198952
Catalog No.:AA00DEYU

4416-57-3 | testololactone

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1mg
3 weeks  
$533.00   $373.00
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10mg
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$2,908.00   $2,035.00
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  • Literature
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA00DEYU
Chemical Name:
testololactone
CAS Number:
4416-57-3
Molecular Formula:
C19H26O3
Molecular Weight:
302.4079
MDL Number:
MFCD00198952
SMILES:
CC12CCC(=O)C=C1CCC3C2CCC4(C3CCC(=O)O4)C
Properties
Computed Properties
 
Complexity:
563  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
5  
Heavy Atom Count:
22  
Hydrogen Bond Acceptor Count:
3  
XLogP3:
2.8  

Literature

Title: Biotransformation of dehydroepiandrosterone (DHEA) with Penicillium griseopurpureum Smith and Penicillium glabrum (Wehmer) Westling.

Journal: Steroids 20101212

Title: Transformation of a series of saturated isomeric steroidal diols by Aspergillus tamarii KITA reveals a precise stereochemical requirement for entrance into the lactonization pathway.

Journal: The Journal of steroid biochemistry and molecular biology 20101101

Title: Transformation of some 3alpha-substituted steroids by Aspergillus tamarii KITA reveals stereochemical restriction of steroid binding orientation in the minor hydroxylation pathway.

Journal: The Journal of steroid biochemistry and molecular biology 20100215

Title: Studies on Baeyer-Villiger oxidation of steroids: DHEA and pregnenolone D-lactonization pathways in Penicillium camemberti AM83.

Journal: Steroids 20091001

Title: Transformation of 5-ene steroids by the fungus Aspergillus tamarii KITA: mixed molecular fate in lactonization and hydroxylation pathways with identification of a putative 3beta-hydroxy-steroid dehydrogenase/Delta5-Delta4 isomerase pathway.

Journal: Biochimica et biophysica acta 20090201

Title: Baeyer-Villiger oxidation of DHEA, pregnenolone, and androstenedione by Penicillium lilacinum AM111.

Journal: Steroids 20081222

Title: Distinct metabolic handling of 3beta-hydroxy-17a-oxa-D-homo-5alpha-androstan-17-one by the filamentous fungus Aspergillus tamarii KITA: Evidence in support of steroid/hydroxylase binding hypothesis.

Journal: Biochimica et biophysica acta 20070901

Title: Ring-B functionalized androst-4-en-3-ones and ring-C substituted pregn-4-en-3-ones undergo differential transformation in Aspergillus tamarii KITA: ring-A transformation with all C-6 substituted steroids and ring-D transformation with C-11 substituents.

Journal: Biochimica et biophysica acta 20060301

Title: Fate of novel Quasi reverse steroidal substrates by Aspergillus tamarii KITA: bypass of lactonisation and an exclusive role for the minor hydroxylation pathway.

Journal: Biochimica et biophysica acta 20050515

Title: [Conversion of androstenedione and androstadienedione by sterol-degrading bacteria].

Journal: Prikladnaia biokhimiia i mikrobiologiia 20040101

Title: Flexibility of the endogenous progesterone lactonisation pathway in Aspergillus tamarii KITA: transformation of a series of cortical steroid analogues.

Journal: The Journal of steroid biochemistry and molecular biology 20031201

Title: Cyclic AMP and the reverse transformation reaction.

Journal: Annals of the New York Academy of Sciences 20020601

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Tags:4416-57-3 Molecular Formula|4416-57-3 MDL|4416-57-3 SMILES|4416-57-3 testololactone