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词条 Dopastin
释义

  1. References

{{Chembox
| ImageFile = Dopastin.svg
| ImageSize =
| SystematicName = (2E)-N(2S)-2-[Hydroxy(nitroso)amino]-3-methylbutyl2-butenamide
| OtherNames =
|Section1={{Chembox Identifiers
| CASNo = 37134-80-8
| PubChem = 6434226
| ChemSpiderID = 4939169
| SMILES = O=C(NC[C@@H](N(O)N=O)C(C)C)/C=C/C
| InChI = 1/C9H17N3O3/c1-4-5-9(13)10-6-8(7(2)3)12(15)11-14/h4-5,7-8,15H,6H2,1-3H3,(H,10,13)/b5-4+/t8-/m1/s1
| InChIKey = FJUBKTNNXRFHFD-WTSVBCDHBR
| StdInChI = 1S/C9H17N3O3/c1-4-5-9(13)10-6-8(7(2)3)12(15)11-14/h4-5,7-8,15H,6H2,1-3H3,(H,10,13)/b5-4+/t8-/m1/s1
| StdInChIKey = FJUBKTNNXRFHFD-WTSVBCDHSA-N
|Section2={{Chembox Properties
| C=9 | H=17 | N=3 | O=3
| Appearance =
| Density =
| MeltingPtC = 116 to 119
| MeltingPt_ref = [1]
| BoilingPt =
| Solubility =
| pKa = 5.1[1]
|Section3={{Chembox Hazards
| MainHazards =
| FlashPt =
| AutoignitionPt =
}}Dopastin is a chemical compound produced by the bacteria Pseudomonas No. BAC-125.[2] It was first isolated and characterized in 1972. It is an inhibitor of the enzyme dopamine β-hydroxylase.[3]

Dopastin can be prepared synthetically from L-valinol.[4]

References

1. ^Merck Index, 11th Edition, 3417
2. ^{{cite journal | pmid = 4648494 | year = 1972 | last1 = Iimura | first1 = H | last2 = Takeuchi | first2 = T | last3 = Kondo | first3 = S | last4 = Matsuzaki | first4 = M | last5 = Umezawa | first5 = H | title = Dopastin, an inhibitor of dopamine -hydroxylase | volume = 25 | issue = 8 | pages = 497–500 | journal = The Journal of Antibiotics | doi=10.7164/antibiotics.25.497}}
3. ^{{cite journal | title = Biochemical and biological studies on dopastin, an inhibitor of dopamine β-hydroxylase |author1=H. Iinuma |author2=M. Matsuzaki |author3=T. Nagatsu |author4=T. Takeuchi |author5=H. Umezawa | journal = Agric. Biol. Chem. | year = 1974 | volume = 38 | pages = 2107–2111 | doi = 10.1271/bbb1961.38.2107 | issue = 11}}
4. ^{{cite journal | doi = 10.1039/C39730000147 | title = Synthesis of dopastin, a dopamine ?-hydroxylase inhibitor of microbial origin | year = 1973 | last1 = Ohno | first1 = M. | last2 = Iinuma | first2 = H. | last3 = Yagisawa | first3 = N. | last4 = Shibahara | first4 = S. | last5 = Suhara | first5 = Y. | last6 = Kondo | first6 = S. | last7 = Maeda | first7 = K. | last8 = Umezawa | first8 = H. | journal = Journal of the Chemical Society, Chemical Communications | issue = 4 | pages = 147 }}
{{Monoamine metabolism modulators}}

2 : Nitrosamines|Dopamine beta hydroxylase inhibitors

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