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词条 7,12-Dimethylbenz(a)anthracene
释义

  1. References

{{Correct title|7,12-Dimethylbenz[a]anthracene|reason=bracket}}{{chembox
| Watchedfields = changed
| Name=7,12-Dimethylbenz[a]anthracene
| verifiedrevid = 477226290
| Reference=[1]
| ImageFile1=DMBA.png
| ImageFile2=7,12-Dimethylbenz(a)anthracene_ballstick.png
| PIN = 7,12-Dimethyltetraphene
| OtherNames = 7,12-Dimethylbenzo[a]phenanthrene
7,12-Dimethylbenzanthracene
7,12-Dimethyltetraphene
1,4-Dimethyl-2,3-benzophenanthrene
|Section1={{Chembox Identifiers
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 5779
| InChI = 1/C20H16/c1-13-16-8-5-6-9-17(16)14(2)20-18(13)12-11-15-7-3-4-10-19(15)20/h3-12H,1-2H3
| InChIKey = ARSRBNBHOADGJU-UHFFFAOYAX
| ChEMBL_Ref = {{ebicite|correct|EBI}}
| ChEMBL = 329673
| StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChI = 1S/C20H16/c1-13-16-8-5-6-9-17(16)14(2)20-18(13)12-11-15-7-3-4-10-19(15)20/h3-12H,1-2H3
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = ARSRBNBHOADGJU-UHFFFAOYSA-N
| CASNo=57-97-6
| CASNo_Ref = {{cascite|correct|CAS}}
| PubChem=6001
| ChEBI_Ref = {{ebicite|correct|EBI}}
| ChEBI = 254496
| SMILES = c32c(c1ccccc1c(c2ccc4c3cccc4)C)C
}}
|Section2={{Chembox Properties
| C=20 | H=16
| Appearance=
| Density=
| MeltingPtC=122 to 123
| BoilingPt=
| Solubility=
|Section3={{Chembox Hazards
| MainHazards=T (Toxic)
| FlashPt=
| AutoignitionPt =
| RPhrases={{R45}} {{R22}}
| SPhrases={{S53}} {{S36/37}} {{S45}}
| NFPA-H = 2
| NFPA-R = 0
| NFPA-F = 0
| NFPA-S =
}}

7,12-Dimethylbenz[a]anthracene (DMBA) is an immunosuppressor and a powerful organ-specific laboratory carcinogen.[2] DMBA is widely used in many research laboratories studying cancer. DMBA serves as a tumor initiator. Tumor promotion can be induced with treatments of 12-O-tetradecanoylphorbol-13-acetate (TPA) in some models of two-stage carcinogenesis.[3] This allows for a greatly accelerated rate of tumor growth, making many cancer studies possible.

References

1. ^7,12-Dimethylbenz(a)anthracene at Sigma-Aldrich
2. ^{{cite journal |author=Miyata M |author2=Furukawa M |author3=Takahashi K |author4=Gonzalez FJ |author5=Yamazoe Y |title=Mechanism of 7, 12-Dimethylbenz[a]anthracene-Induced Immunotoxicity: Role of Metabolic Activation at the Target Organ |journal=Jpn J Pharmacol |date=2001 |volume=86 |pages=302–309 |url=http://sciencelinks.jp/j-east/article/200201/000020020101A0826695.php |doi=10.1254/jjp.86.302 |deadurl=yes |archiveurl=https://web.archive.org/web/20100117042118/http://sciencelinks.jp/j-east/article/200201/000020020101A0826695.php |archivedate=2010-01-17 |df= }}
3. ^{{cite journal | author = Sung YM | author2 = He G | author3 = Fischer, SM | date = 2005 | title = Lack of Expression of the EP2 but not EP3 Receptor for Prostaglandin E2 Results in Suppression of Skin Tumor Development | journal = Cancer Res | volume = 65 | pages = 9304–9311 | doi=10.1158/0008-5472.can-05-1015}}

4 : Polycyclic aromatic hydrocarbons|Carcinogens|Anthracenes|Immunosuppressants

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