推荐产品
化驗
≥99.0% (sum of enantiomers, GC)
形狀
solid
光學活性
[α]20/D −71±1°, c = 2% in chloroform
mp
61-63 °C
62-63 °C (lit.)
應用
metabolomics
vitamins, nutraceuticals, and natural products
儲存溫度
2-8°C
SMILES 字串
[H][C@@]12CCC(=C)[C@@]3([H])CC(C)(C)[C@]3([H])CC[C@@]1(C)O2
InChI
1S/C15H24O/c1-10-5-6-13-15(4,16-13)8-7-12-11(10)9-14(12,2)3/h11-13H,1,5-9H2,2-4H3/t11-,12-,13-,15-/m1/s1
InChI 密鑰
NVEQFIOZRFFVFW-RGCMKSIDSA-N
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一般說明
(−)-石竹烯氧化物或β-石竹烯氧化物(BCPO)是一种天然植物化合物:二环倍半萜,是β-石竹烯(BCP)的氧化衍生物。它有强烈的木材气味。BCPO 通常存在于许多食品和香料植物和精油中,如罗勒、鼠尾草和丁香。它被广泛用作化妆品和食品添加剂。
應用
(−)-石竹烯氧化物已用作:
- 抗菌剂,研究其对革兰氏阳性、革兰氏阴性及酵母菌的抑菌效果
- 作为商业标准品,使用气相色谱-火焰电离检测(GC-FID)对地钱提取物的成分进行定量分析。
- 作为参考标准品,采用气相色谱-质谱联用(GC-MS)技术分析 Achillea ligustica 精油成分的对映体比例。
生化/生理作用
β-石竹烯氧化物是一种有效的抗癌剂,还具有抗氧化、抗炎和抗病毒的特性。它是大鼠和人肝微粒体中药物代谢酶P4503A(CYP3A)活性的强抑制剂。BCPO 还具有镇痛、抗真菌、抗菌和基因保护活性。
其他說明
精心纯化的倍半萜烯;立体选择性重排为烯丙醇;转化为胺
訊號詞
Warning
危險聲明
危險分類
Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 2
閃點(°F)
230.0 °F - closed cup
閃點(°C)
110 °C - closed cup
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
其他客户在看
Synlett, 337-337 (1991)
Natural product communications, 5(9), 1365-1368 (2010-10-07)
Commercially available aroma samples were evaluated for their olfactory quality by professional perfumers and tested for their antimicrobial activity. Agar diffusion and agar-dilution were used as test methods and a set of two Gram-positive (Staphylococcus aureus and Enterococcus faecalis) and
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The endocannabinoid system (ECS), a conserved physiological system emerged as a novel pharmacological target for its significant role and potential therapeutic benefits ranging from neurological diseases to cancer. Among both, CB1 and CB2R types, CB2R have received attention for its
Chemico-biological interactions, 278, 123-128 (2017-10-28)
Sesquiterpenes, the main components of plant essential oils, are often taken in the form of folk medicines and dietary supplements. Several sesquiterpenes possess interesting biological activities but they could interact with concurrently administered drugs via inhibition of drug-metabolizing enzymes. Therefore
Tetrahedron, 49, 4183-4183 (1993)
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