Zeatin

Zeatin

Names
IUPAC name (E)-2-methyl-4-(7H-purin-6-ylamino)but-2-en-1-ol
Identifiers
CAS Number	1637-39-4 Y
3D model (JSmol)	Interactive image
ChEBI	CHEBI:16522 N
ChemSpider	395716 N
PubChem CID	449093
UNII	7I6OOJ9GR6 Y
CompTox Dashboard (EPA)	DTXSID10859662
InChI InChI=1S/C10H13N5O/c1-7(4-16)2-3-11-9-8-10(13-5-12-8)15-6-14-9/h2,5-6,16H,3-4H2,1H3,(H2,11,12,13,14,15)/b7-2+ N Key: UZKQTCBAMSWPJD-FARCUNLSSA-N N InChI=1/C10H13N5O/c1-7(4-16)2-3-11-9-8-10(13-5-12-8)15-6-14-9/h2,5-6,16H,3-4H2,1H3,(H2,11,12,13,14,15)/b7-2+ Key: UZKQTCBAMSWPJD-FARCUNLSBM
SMILES C/C(=C\CNC1=NC=NC2=C1NC=N2)/CO
Properties
Chemical formula	C10H13N5O
Molar mass	219.248 g·mol−1
Appearance	Off-white to yellow crystalline powder
Melting point	208 to 210 °C (406 to 410 °F; 481 to 483 K)
Solubility in 1M NaOH	Soluble
Hazards
Lethal dose or concentration (LD, LC):
LD50 (median dose)	2200 mg/kg (mouse, transperitoneal)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is YN ?) Infobox references

Zeatin is a cytokinin derived from adenine, which occurs in the form of a cis- and a trans-isomer and conjugates. Zeatin was discovered in immature corn kernels from the genus Zea. It promotes growth of lateral buds and when sprayed on meristems stimulates cell division to produce bushier plants.^{[citation needed]}