12436
Neryl pyrophosphate lithium salt
≥95.0% (TLC)
동의어(들):
(Z)-3,7-Dimethyl-2,6-octadien-1-yl pyrophosphate lithium salt, Neryl diphosphate lithium salt
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모든 사진(1)
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1 G
$116.00
25 G
$1,110.00
100 G
$3,140.00
1 KG
$4,665.00
About This Item
실험식(Hill 표기법):
C10H20O7P2 · xLi+
CAS Number:
Molecular Weight:
314.21 (free acid basis)
MDL number:
UNSPSC 코드:
12352107
NACRES:
NA.25
추천 제품
관련 카테고리
1 of 4
이 품목 | A9085 | A2934 | A3156 |
|---|---|---|---|
| biological source bovine | biological source bovine | biological source bovine | biological source bovine |
| technique(s) ELISA: suitable, cell culture | mammalian: suitable | technique(s) flow cytometry: suitable, immunofluorescence: suitable | technique(s) ELISA: suitable | technique(s) cell culture | mammalian: suitable |
| assay ≥98% (agarose gel electrophoresis) | assay ≥96% (agarose gel electrophoresis) | assay ≥98% (agarose gel electrophoresis) | assay ≥99% (agarose gel electrophoresis) |
| Quality Level 200 | Quality Level 200 | Quality Level 200 | Quality Level 200 |
| form lyophilized powder | form lyophilized powder | form lyophilized powder | form lyophilized powder |
애플리케이션
Neryl pyrophosphate, the cis isomer of geranyl pyrophosphate, may be used to characterize and study the kinetics of enzymes such as 1,8-cineole synthase, farnesyl pyrophosphate synthase, pinene cyclase and geranyl pyrophosphate:sabinene hydrate cyclase.
생화학적/생리학적 작용
Metabolite, substrate for monoterpene synthase.[1]
포장
Bottomless glass bottle. Contents are inside inserted fused cone.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
가장 최신 버전 중 하나를 선택하세요:
T W Hallahan et al.
Archives of biochemistry and biophysics, 264(2), 618-631 (1988-08-01)
A soluble enzyme preparation from the leaves of sweet marjoram (Majorana hortensis Moench) catalyzes the divalent cation-dependent cyclization of [1-3H]geranyl pyrophosphate to the bicyclic monoterpene alcohols (+)-[6-3H]cis- and (+)-[6-3H]-transsabinene hydrate, providing labeling patterns consistent with current mechanistic considerations. No free
R Croteau et al.
Archives of biochemistry and biophysics, 309(1), 184-192 (1994-02-15)
Geranyl pyrophosphate: 1,8-cineole cyclase (cineole synthase) catalyzes the conversion of geranyl pyrophosphate to the symmetrical monoterpene ether 1,8-cineole (1,3,3-trimethyl-2-oxabicyclo[2.2.2]octane) by a process thought to involve the initial isomerization of the substrate to the tertiary allylic isomer, linalyl pyrophosphate, and cyclization
D R Light et al.
The Journal of biological chemistry, 264(31), 18598-18607 (1989-11-05)
A prenyltransferase purified from the commercial rubber tree, Hevea brasiliensis, that elongates existing cis-polyisoprene rubber molecules also catalyzes the formation of all trans-farnesyl pyrophosphate (t,t-FPP) from dimethylallyl pyrophosphate (DMAPP) and isopentenyl pyrophosphate (IPP). In assays of the latter activity trans-geranyl
R Croteau et al.
The Journal of biological chemistry, 264(26), 15309-15315 (1989-09-15)
(+)-Pinene cyclase from sage (Salvia officinalis) catalyzes the isomerization and cyclization of geranyl pyrophosphate to (+)-alpha-pinene and (+)-camphene, and to lesser amounts of (+)-limonene, myrcene, and terpinolene, whereas (-)-pinene cyclase from this tissue catalyzes the conversion of the acyclic precursor
Old substrates for new enzymes of terpenoid biosynthesis.
Jörg Bohlmann et al.
Proceedings of the National Academy of Sciences of the United States of America, 106(26), 10402-10403 (2009-06-26)
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