334491-30-4

Basic information

• Product Name: (23S,25R)-5α-spirostan-3β,6β,23-triol
• CAS NO: 334491-30-4
• Molecular Weight: 448.643
• Mol File: 334491-30-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (23S,25R)-5α-spirostan-3β,6β,23-triol(CAS DataBase Reference)
• NIST Chemistry Reference: (23S,25R)-5α-spirostan-3β,6β,23-triol(334491-30-4)
• EPA Substance Registry System: (23S,25R)-5α-spirostan-3β,6β,23-triol(334491-30-4)

Safety Data

• Hazardous Substances Data: 334491-30-4(Hazardous Substances Data)

Upstream product

• 3514-56-5 (25R)-5α-spirostan-3β,6β-diyl diacetate 
• 3514-59-8 (25R)-5α-spirostan-3,6-dione 
• 512-04-9 diosgenin 
• 41743-71-9 (3β,5α,6β,25R)-spirostan-3,6-diol 
• 511-91-1 chlorogenin 
• 221369-57-9 (25R)-3β,6β-diacetoxy-5α-spirostan-23-one 
• 221369-53-5 (23S,25R)-5α-spirostan-3β,6β,23-triol 3,6-diacetate 

Relevant articles and documents

Spirostanic analogues of teasterone. Synthesis, characterisation and biological activity of laxogenin, (23S)-hydroxylaxogenin and 23-ketolaxogenin (23-oxolaxogenin)

The synthesis and characterization of the naturally occurring steroid sapogenin laxogenin and its derivatives 23-ketolaxogenin and (23S)-hydroxylaxogenin were described. Compounds reported have shown plant-growth-stimulating activity in tests and field trials. The effect consisted of an increase of the length of the treated hypocotyls compared with that of the non-treated plants. Results showed that when the same solutions were applied to the seeds of orange tree, a strong promotion of the germination was observed.