| 词条 | Carbapenam |
| 释义 |
| ImageFile = Carbapenam structure.svg | ImageSize = 150px | IUPACName = 1-Azabicyclo[3.2.0]heptan-7-one | OtherNames = |Section1={{Chembox Identifiers | CASNo = 23806-36-2 | CASNo_Ref = {{cascite|correct|}} | CASNo1 = 73429-58-0 | CASNo1_Ref = {{cascite|correct|}} | CASNo1_Comment = (R) | CASNo2 = 67506-08-5 | CASNo2_Ref = {{cascite|correct|}} | CASNo2_Comment = (S) | PubChem = 549337 | ChemSpiderID = 477976 | SMILES = O=C1N2C(C1)CCC2 | InChI = 1/C6H9NO/c8-6-4-5-2-1-3-7(5)6/h5H,1-4H2 | InChIKey = INAHHIFQCVEWPW-UHFFFAOYAR | StdInChI = 1S/C6H9NO/c8-6-4-5-2-1-3-7(5)6/h5H,1-4H2 | StdInChIKey = INAHHIFQCVEWPW-UHFFFAOYSA-N |Section2={{Chembox Properties | C=6 | H=9 | N=1 | O=1 | Appearance = | Density = | MeltingPt = | BoilingPt = | Solubility = |Section3={{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }} A carbapenam is a β-lactam compound that is a saturated carbapenem.[1] They exist primarily as biosynthetic intermediates on the way to the carbapenem antibiotics. {{clear-left}}References1. ^{{Cite journal | last1 = Dalhoff | first1 = A. | last2 = Janjic | first2 = N. | last3 = Echols | first3 = R. | title = Redefining penems | doi = 10.1016/j.bcp.2005.12.003 | journal = Biochemical Pharmacology | volume = 71 | issue = 7 | pages = 1085–1095 | year = 2006 | pmid = 16413506}} {{heterocyclic-stub}} 1 : Carbapenem antibiotics |
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