2312-73-4
Chemical Structure
BAP9THP
Synonym(s): SD 8339; N-Benzyl-9-(tetrahydro-2h-pyran-2-yl)adenine
- CAS No.: 2312-73-4
- Formula:C17H19N5O
- Molecular Weight:309.37
IUPAC Name: N-benzyl-9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-amine
InChIKey: POFWRMVFWIJXHP-UHFFFAOYSA-N
SMILES: N1(C=NC2=C(N=CN=C12)NCC3=CC=CC=C3)C4CCCCO4
Biological Activity: BAP9THP is a synthetic cytokinin derivative and a growth regulator. BAP9THP promotes chlorophyll retention (and senescence delay) in plant tissues exceptionally strongly, and growth of tobacco callus almost as strongly as 6-Benzylaminopurine (BAP). BAP9THP induces adventitious shoot formation ignificantly more strongly than N6-isopentenyladenine or Kinetin[1][2].
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BAP9THP | 99.92% | BAP9THP is a synthetic cytokinin derivative and a growth regulator. BAP9THP promotes chlorophyll retention (and senescence delay) in plant tissues exceptionally strongly, and growth of tobacco callus almost as strongly as 6-Benzylaminopurine (BAP). BAP9THP induces adventitious shoot formation ignificantly more strongly than N6-isopentenyladenine or Kinetin. | ||||||||||||||||||||
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BAP9THP (Standard) | ≥98% | BAP9THP (Standard) is the analytical standard of BAP9THP. This product is intended for research and analytical applications. BAP9THP is a synthetic cytokinin derivative and a growth regulator. BAP9THP promotes chlorophyll retention (and senescence delay) in plant tissues exceptionally strongly, and growth of tobacco callus almost as strongly as 6-Benzylaminopurine (BAP). BAP9THP induces adventitious shoot formation ignificantly more strongly than N6-isopentenyladenine or Kinetin. | ||||||||||||||||||||
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- [1]. Smýkalová, I., et al. The effects of novel synthetic cytokinin derivatives and endogenous cytokinins on the in vitro growth responses of hemp (Cannabis sativa L.) explants. Plant Cell Tiss Organ Cult 139, 381–394 (2019).
- [2]. Vylíčilová H, et al. Naturally Occurring and Artificial N9-Cytokinin Conjugates: From Synthesis to Biological Activity and Back. Biomolecules. 2020;10(6):832. Published 2020 May 29. [Content Brief]
Keywords
