8066-07-7|Xanthoxin|Xanthoxin|-范德生物科技公司

Xanthoxin

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names：
Xanthoxin
CAS号：
8066-07-7
MDL Number：
MF(分子式)： C15H22O3 MW(分子量)： 250.33
EINECS:232-513-2 Reaxys Number:
Pubchem ID:5282222 Brand:BIOFOUNT

Xanthoxin（8066-07-7）中文名:2-顺式，4-反式黄嘌呤毒素是载脂蛋白类胡萝卜素倍半萜和烯醛。Xanthoxin具有植物生长抑制剂和植物代谢产物的作用。Xanthoxin还是植物激素脱落酸的生物合成中间体。

货品编码	规格	纯度	价格 (¥)	现价(¥)	特价(¥)	库存描述	数量	总计 (¥)
HCC353086-10mg	10mg	97%	¥ 116375.00	¥ 116375.00		4-7周	- +	¥ 0.00

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中文别名	Xanthoxin（8066-07-7）,[1S-[1α(2Z,4E),4α,6α]]-5-(4-Hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]hept-1-yl)-3-methyl-2,4-pentadienal; 7-Oxabicyclo[4.1.0]heptane, 2,4-pentadienal deriv.; (-)-Xanthoxin; 2-cis,4-trans-Xanthoxin; XAN; Xanthoxal; cis,trans-Xanthoxin
英文别名	Xanthoxin;2-cis,4-trans-Xanthoxin（8066-07-7）;(1R-(1alpha(2E,4E),4beta,6alpha))-isomer
CAS号	8066-07-7
SMILES	C/C(=C/C=O)/C=C/[C@]12[C@](O1)(C[C@H](CC2(C)C)O)C
Inchi	InChI=1S/C15H22O3/c1-11(6-8-16)5-7-15-13(2,3)9-12(17)10-14(15,4)18-15/h5-8,12,17H,9-10H2,1-4H3/b7-5+,11-6-/t12-,14+,15-/m0/s1
InchiKey	ZTALKMXOHWQNIA-TVBSHJCBSA-N
分子式 Formula	C15H22O3
分子量 Molecular Weight	250.33
闪点 FP	132.6±20.0 °C
熔点 Melting point	No data available
沸点 Boiling point	371.1±37.0 °C at 760 mmHg
Polarizability极化度	28.7±0.5 10-24cm3
密度 Density	1.2±0.1 g/cm3
蒸汽压 Vapor Pressure	0.0±1.9 mmHg at 25°C
溶解度Solubility
性状	solid power
储藏条件 Storage conditions	Sotre at -20℃

产品说明	Xanthoxin(CAS:8066-07-7):具有植物生长抑制剂和植物代谢产物的作用，Xanthoxin其它参数见主页
Introduction	Xanthoxin(CAS:8066-07-7):only use for non-medical purposes in industrial or scientific research, and not for clinical diagnosis and treatment of humans or animals. This product is not medicinal or edible.
Application1	黄嘌呤毒素在许多植物中都是内源性的，并且在植物组织和无细胞系统中被代谢为ABA。
Application2	Xanthoxin is a growth inhibitor in plants.
Application3

警示图
危险性
危险性警示	No data available
安全声明	P313
安全防护
备注

Control of abscisic acid synthesis PMID 11006307; Journal of experimental botany 2000 Sep; 51(350):1563-74

Abscisic acid, xanthoxin and violaxanthin in the caps of gravistimulated maize roots PMID 11540889; Planta 1985; 166(1):483-9

Abscisic acid, xanthoxin and violaxanthin in the caps of gravistimulated maize roots PMID 24241613; Planta 1985 Dec; 166(4):483-9

The short-chain alcohol dehydrogenase ABA2 catalyzes the conversion of xanthoxin to abscisic aldehyde PMID 12172025; The Plant cell 2002 Aug; 14(8):1833-46

Formation and breakdown of ABA PMID 10562731; Trends in plant science 1999 Dec; 4(12):472-478

Xanthoxin Metabolism in Cell-free Preparations from Wild Type and Wilty Mutants of Tomato.Ram K. Sindhu, Daniel C.Walton.September 1988

Abstract:Extracts prepared from the turgid and water-stressed leaves of wild-type tomato (Lycopersicon esculentum Mill cv Ailsa Craig) and the wilty mutants sitiens, notabilis, and flacca were tested for their ability to metabolize xanthoxin to ABA. Extracts from wild type and notabilis converted xanthoxin at similar rates, while extracts from sitiens and flacca showed little or no activity. We also observed no activity when extracts of sitiens and flacca were mixed. Similar results were obtained when ABA aldehyde was used as a substrate, in that extracts from wild type and notabilis were equally active, but extracts from flacca and sitiens showed little activity. None of the tomato extracts showed significant activity with xanthoxin acid, xanthoxin alcohol, or ABA-1′,4-′Trans-diol as substrates. Extracts from bean leaves (Phaseolus vulgaris L. cv Blue Lake) were similar to the wild-type tomato extracts in their ability to convert the various substrates to ABA, although excised bean leaves did convert ABA-1′,4′-trans-diol and xanthoxin alcohol to ABA when these substances were taken up through the petiole. These results are consistent with a role for xanthoxin as a normal intermediate on the ABA biosynthetic pathway, and they suggest that ABA aldehyde is the final ABA precursor.

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