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17397-89-6

中文名稱 淺藍(lán)菌素
英文名稱 CERULENIN
CAS 17397-89-6
分子式 C12H17NO3
分子量 223.27
MOL 文件 17397-89-6.mol
更新日期 2026/05/25 12:49:33
17397-89-6 結(jié)構(gòu)式 17397-89-6 結(jié)構(gòu)式

基本信息

中文別名
淺藍(lán)菌素
天藍(lán)菌素
變藍(lán)菌素
2,3-環(huán)氧-4-氧-7,10-十二碳二烯酰胺
2,3-環(huán)氧-4-氧-7,10-十二碳二烯酰胺/變藍(lán)菌素/天藍(lán)菌素
英文別名
Crl
CERULENIN
Nsc116069
Aids000236
helicocerin
Aids-000236
CERULENIN USP/EP/BP
Cerulenin (Synthetic)
2,3-epoxy-4-oxo-10-dodecadienamide
CERULENIN, CEPHALOSPORIUM CAERULENS
所屬類別
原料藥:其它抗生素類藥

物理化學(xué)性質(zhì)

熔點(diǎn)93.5℃
比旋光度D16 +63° (c = 2 in methanol)
沸點(diǎn)bp 120° (10-8 mm)
密度1.1223 (rough estimate)
折射率1.5300 (estimate)
儲(chǔ)存條件−20°C
溶解度acetone: 20 mg/mL, clear, colorless to yellow
酸度系數(shù)(pKa)15.19±0.40(Predicted)
形態(tài)白色至灰白色固體
顏色米白色
Merck13,2014
BRN4140423
穩(wěn)定性可在-20°下的DMSO或乙醇溶液保存長(zhǎng)達(dá)1個(gè)月。
InChI1S/C13H18O3/c1-3-4-5-6-7-8-9-11(15)13-12(16-13)10(2)14/h3-4,6-7,12-13H,5,8-9H2,1-2H3/b4-3+,7-6+/t12-,13+/m0/s1
InChIKeyPTNNGEBMCNMENY-JIVMHGEESA-N
SMILESC/C=C/C/C=C/CCC([C@@H]1[C@H](C(N)=O)O1)=O

安全數(shù)據(jù)

危險(xiǎn)性符號(hào)(GHS)有害 (GHS07)
GHS07
警示詞警告
危險(xiǎn)性描述H302
防范說(shuō)明P264-P270-P301+P312-P501
危險(xiǎn)品標(biāo)志Xn
危險(xiǎn)類別碼22
安全說(shuō)明24/25
WGK Germany3
RTECS號(hào)JR1670000
海關(guān)編碼29419090
存儲(chǔ)類別11 - Combustible Solids
危險(xiǎn)性類別Acute Tox. 4 Oral
毒性LD50 in mice (mg/kg): 154 i.v.; 211 i.p.; 547 orally (Matsumae 1964)
淺藍(lán)菌素價(jià)格(試劑級(jí))
報(bào)價(jià)日期產(chǎn)品編號(hào)產(chǎn)品名稱CAS號(hào)包裝價(jià)格
2026/06/05HY-A0210淺藍(lán)菌素
Cerulenin
17397-89-61 mg906元
2026/06/05HY-A0210淺藍(lán)菌素
Cerulenin
17397-89-65mg2380元
2026/06/05HY-A0210淺藍(lán)菌素
Cerulenin
17397-89-610mM * 1mLin DMSO2618元

常見問(wèn)題列表

生物活性
Cerulenin 是一種廣泛使用的天然脂肪酸合成酶 (FASN) 抑制劑。Cerulenin 是由真菌 Cephalosporium caeruleus 產(chǎn)生的。
靶點(diǎn)

Fatty acid synthase (FASN)

體外研究

Cerulenin covalently binds to the catalytic site of FAS and disrupts the condensation reaction of acetyl-COA and malonyl-COA, inhibiting the biosynthesis of fatty acids and sterols in yeast. The Flavonoids quercetin and trans-Chalcone are effective against T. rubrum , with MICs of 125 and 7.5 μg/mL for the wild-type strain (MYA3108) and of 63 and 1.9 μg/mL for the ABC transporter mutant strain (Δ TruMDR2 ), respectively. The MICs of the Fluconazole and Cerulenin controls are 63 and 125 μg/mL for the wild-type strain and 30 and 15 μg/mL for the mutant strain, respectively. To explore the underlying mechanism of Steroidogenic acute regulatory protein (StAR)’s protective effect on endothelial dysfunction model, the inhibitor of fatty acid synthase and HMG-CoA reductase, Cerulenin ( 5 μg/mL) and Lovastatin, are used before palmitic acid (PA) added. The mRNA expression of IL-1β, TNFα, VCAM-1 and IL-6 are reduced while NO production is recovered with inhibitor treatment.

體內(nèi)研究

Cerulenin treatment of ob/ob mice has obvious effects on body weight. With 2 days of treatment, body weight in treated mice is decreased compared to a 5.7% weight gain in the controls. With prolonged (7 days) treatment, no body weight loss is observed, but body weight gain is slowed. In all groups, 60 mg/kg of Cerulenin is more effective than 30 mg/kg in inhibiting weight gain. If given daily or every other day, ATP content are increased 58.1% and 61.5% respectively by 7-day treatment of 60 mg/kg Cerulenin. Significant ATP elevation is also observed with only 2 days of treatment with 60 mg/kg Cerulenin. In contrast, 30 mg/kg Cerulenin, given either 2 or 7 days, does not show any significant effect on cellular ATP content.

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