-
Xanthoxin
- names:
Xanthoxin
- CAS號:
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
| 貨品編碼 | 規(guī)格 | 純度 | 價格 (¥) | 現(xiàn)價(¥) | 特價(¥) | 庫存描述 | 數(shù)量 | 總計 (¥) |
|---|---|---|---|---|---|---|---|---|
| HCC353086-10mg | 10mg | 97% | ¥ 116375.00 | ¥ 116375.00 | 4-7周 | ¥ 0.00 |
| 中文別名 | 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 |
| 英文別名 | Xanthoxin;2-cis,4-trans-Xanthoxin(8066-07-7);(1R-(1alpha(2E,4E),4beta,6alpha))-isomer |
| CAS號 | 8066-07-7 |
| 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 |
| 溶解度Solubility | |
| 性狀 | solid power |
| 儲藏條件 Storage conditions | Sotre at -20℃ |
| 產(chǎn)品說明 | Xanthoxin(CAS:8066-07-7):具有植物生長抑制劑和植物代謝產(chǎn)物的作用,Xanthoxin其它參數(shù)見主頁 |
| 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 | 黃嘌呤毒素在許多植物中都是內(nèi)源性的,并且在植物組織和無細胞系統(tǒng)中被代謝為ABA。 |
| Application2 | Xanthoxin is a growth inhibitor in plants. |
| Application3 |
| 警示圖 | |
| 危險性 | |
| 危險性警示 | No data available |
| 安全聲明 | P313 |
| 安全防護 | |
| 備注 |
| 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.- 相關(guān)產(chǎn)品
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