推薦產品
化驗
≥98%
mp
245-247 °C (lit.)
SMILES 字串
Oc1ccc2C(=O)C=C(Oc2c1)c3ccccc3
InChI
1S/C15H10O3/c16-11-6-7-12-13(17)9-14(18-15(12)8-11)10-4-2-1-3-5-10/h1-9,16H
InChI 密鑰
MQGPSCMMNJKMHQ-UHFFFAOYSA-N
基因資訊
mouse ... Hexa(15211)
rat ... Ar(24208) , Gabra2(29706)
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應用
作为如下过程的反应物：
- 在 O-糖基化反应中作为具有生物学价值的受体
- 参与合成完全磷酸化的黄酮类化合物，用作胰腺胆固醇酯酶抑制剂
- 用于碳酸二甲酯的 O-甲基化
- 通过多亚甲基链连接，合成 α1-肾上腺素受体拮抗剂
- 参与 Baylis-Hillman 反应
- 参与相转移催化的糖基化反应，合成糖基化的类黄酮
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
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Chemical & pharmaceutical bulletin, 54(3), 320-324 (2006-03-02)
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A central part (amino-acid position 268-397 of 458 amino-acid residues) of the biphenyl dioxygenase large (alpha) subunit, BphA1, from Pseudomonas pseudoalcaligenes strain KF707 was exchanged with the corresponding part of BphA1 from another biphenyl-degrading bacterium, Pseudomonas putida strain KF715, to
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Four flavones (flavone, 7-hydroxyflavone, chrysin, and baicalein) sharing the same B- and C-ring structure but a different numbers of hydroxyl groups on the A-ring were studied for their affinities for BSA and HSA. The hydroxylation on ring A of flavones
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