82-08-6
中文名稱
粗糠柴苦素
英文名稱
ROTTLERIN
CAS
82-08-6
EINECS 編號
201-395-4
分子式
C30H28O8
MDL 編號
MFCD00017361
分子量
516.54
MOL 文件
82-08-6.mol
更新日期
2026/02/25 13:56:15
82-08-6 結(jié)構(gòu)式
基本信息
中文別名
粗糠柴苦素咖馬林/粗糠柴苦素
咖馬林
英文別名
3'-[(8-CINNAMOYL-5,7-DIHYDROXY-2,2-DIMETHYL-2H-1-BENZOPYRAN-6-YL)METHYL]-2',4',6'-TRIHYDROXY-5'-METHYLACETOPHENONEMALLOTOXIN
ROTTLERIN
4’,6’-trihydroxy-5’-methyl-methyl)-2
acetophenone,3’-((8-cinnamoyl-5,7-dihydroxy-2,2-dimethyl-2h-1-benzopyran-6-yl)
kamalin
(E)-1-[6-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-5,7-dihydroxy-2,2-dimethyl-2H-1-benzopyran-8-yl]-3-phenyl-2-propen-1-one
2-Propen-1-one, 1-[6-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-5,7-dihydroxy-2,2-dimethyl-2H-1-benzopyran-8-yl]-3-phenyl-, (2E)-
1-[6-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-5,7-dihydroxy-2,2-dimethyl-2h-1-benzopyran-8-yl]-3-phenyl-2-propen-1-one
3'-[(8-Cinnamoyl-5,7-dihydroxy-2,2-dimethyl-2H-1-benzopyran-6-yl)methyl]-2',4',6'-trihydroxy-5'-methylacetophenone
所屬類別
生物化工：提取物物理化學(xué)性質(zhì)
熔點200 °C
熔點200 °C
沸點521.39°C (rough estimate)
密度1.2051 (rough estimate)
折射率1.4900 (estimate)
儲存條件2-8°C
儲存條件2-8°C
溶解度溶于DMSO（高達(dá)50mg/ml）。
酸度系數(shù)(pKa)6.92±0.40(Predicted)
形態(tài)粉末
顏色橙色到棕色
生物來源plant (Mallotus philippinensis)
穩(wěn)定性DMSO中的溶液可在-20°下穩(wěn)定儲存1個月。
InChIKeyDEZFNHCVIZBHBI-ZHACJKMWSA-N
SMILESO1C(C=Cc2c1c(c(c(c2O)Cc4c(c(c(c(c4O)C(=O)C)O)C)O)O)C(=O)\C=C\c3ccccc3)(C)C
LogP8.660 (est)
CAS 數(shù)據(jù)庫82-08-6(CAS DataBase Reference)
安全數(shù)據(jù)
危險品標(biāo)志Xn
危險類別碼20/21/22-22
危險類別碼R20/21/22
安全說明36/37-24/25
安全說明S36/37
WGK Germany3
WGK Germany3
RTECS號AM6913800
海關(guān)編碼29329990
存儲類別11 - Combustible Solids
粗糠柴苦素價格(試劑級)
| 報價日期 | 產(chǎn)品編號 | 產(chǎn)品名稱 | CAS號 | 包裝 | 價格 |
| 2026/07/06 | 32849 | 粗糠柴毒素 Rottlerin, 95+%, Thermo Scientific Chemicals | 82-08-6 | 10mg | 1309元 |
| 2026/07/06 | S7862 | 粗糠柴苦素 Rottlerin | 82-08-6 | 5mg | 970.17元 |
| 2026/07/06 | S7862 | 粗糠柴苦素 Rottlerin | 82-08-6 | 25mg | 2970.13元 |
常見問題列表
生物活性
Rottlerin (Mallotoxin, NSC 56346, NSC 94525)是一種從 Mallotus Philippinensis 純化出來的天然化合物，一種特效的 Protein kinase 的抑制劑，對PKCδ(來自桿狀病毒感染的Sf9昆蟲細(xì)胞)、PKCδ(來自豬脾)和CaM kinase III的IC50值分別為3 μM、6 μM和5.3 μM。Rottlerin 還可以抑制PKCα、PKCγ、PKCβ、PKCη、CKII和PKA，其IC50值分別為30 μM、40 μM、42 μM、82 μM、30 μM和78 μM。靶點
| Target | Value |
|
PKCδ
(Cell-free assay) | 3 μM |
|
CKIII
(Cell-free assay) | 5.3 μM |
|
PKCα
(Cell-free assay) | 30 μM |
|
CKII
(Cell-free assay) | 30 μM |
|
PKCγ
(Cell-free assay) | 40 μM |
體外研究
Rottlerin (20 μM, 2/6/24 hours) dramatically decreases the cyclin D-1 mRNA levels in a time-dependent manner in primary HMVEC.
Rottlerin (20 μM) exhibits cell proliferation in HMVEC.
Western Blot Analysis
| Cell Line: | Primary HMVEC (Human Microvascular Endothelial Cell). |
| Concentration: | 20 μM. |
| Incubation Time: | 2, 6, 24 hours. |
| Result: | Dramatically decreased the cyclin D-1 mRNA levels in a time-dependent manner. After 2 h of treatment, the mRNA level was reduced to 50% of the control, to circa 40% after 6 h, and to 20% after 24 h. Consistently, a similar trend was observed in the protein levels, where the decrease was circa 50% after 2 h, 80% after 6 h, and to almost undetectable levels after 24 h. |
Cell Proliferation Assay
| Cell Line: | Primary HMVEC (Human Microvascular Endothelial Cell). |
| Concentration: | 20 μM. |
| Incubation Time: | 24/48 hours. |
| Result: | Exhibited a strong growth inhibition, with a reduction in thymidine incorporation respect to the control cells (DMSO 0.1%) of circa 75% and 80%, respectively. |
體內(nèi)研究
Rottlerin (20 mg/kg, gavage 5 days per week, once daily, for 6 weeks) inhibits AsPC-1 pancreatic tumor growth in Balb C nude mice with no toxicity.
Rottlerin inhibits tumor cell proliferation, and induces apoptosis through activation of caspase-3 and cleavage of poly(ADP-ribose) polymerase (PARP).
| Animal Model: | Balb C nude mice (4-6 weeks old) with AsPC-1 cells (2×10 6 cells mixed with Matrigel, 50:50 ratio) injection. |
| Dosage: | 0 or 20 mg/kg. |
| Administration: | Gavage 5 days per week, once daily, for 6 weeks. |
| Result: | Inhibited AsPC-1 pancreatic tumor growth in Balb C nude mice and had no effect on the body weight of AsPC-1 tumor-bearing mice. |