ライフサイエンスコーパス: phenanthridine

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1 iplatin, cis-[Pt(NH3)2(Am)Cl](+) where Am is phenanthridine.

2 useful alternative for preparing substituted phenanthridines.

3 ly known phenanthro[9',10':4,5]imidazo[1,2-f]phenanthridines.

4 enant hridium chloride (NK314) is a benzo[c] phenanthridine alkaloid that inhibits topoisomerase IIal

5 Bioactive indolo[3,2-j]phenanthridine alkaloids Calothrixin A and B have been s

6 with the total synthesis of four oxybenzo[c]phenanthridine alkaloids, oxychelerythrine, oxysanguinar

7 lorine (2d), trispheridine (2b), and benzo[c]phenanthridines alkaloids dihydronitidine (3b), dihydroc

8 n, thus offering an expeditious route to the phenanthridine and benzo[c]phenanthridine skeletons.

9 intermediates in the biosynthesis of benzo[c]phenanthridine and rhoeadine derivatives.

10 A novel and efficient synthesis of phenanthridines and aza analogues is reported.

11 ymes in the metabolism of protopine, benzo[c]phenanthridine, and rhoeadine alkaloids.

12 Phenanthro[9',10':4,5]imidazo[1,2-f]phenanthridines are blue-emitters, and they exhibit stro

13 The arylation products can be converted to phenanthridines by the reaction with trifluoroacetic anh

14 ated was phenanthriplatin, cis-[Pt(NH(3))(2)(phenanthridine)Cl]NO(3), which exhibits significantly gr

15 Starting from the nonsubstituted phenanthridine compound 4a, exhibiting a K(i) value of 5

16 Here we report on a phenanthridine derivative which has a covalently linked

17 the probe being over 5x brighter than other phenanthridine derivatives when bound to RNA.

18 nsfer efficiency from the fluorescein to the phenanthridine fluorophore is approximately 77%, which r

19 ee approach for the synthesis of substituted phenanthridines from the coupling reaction of aryldiazon

20 iplatin, where Am is the N-heterocyclic base phenanthridine, has promising anticancer activity.

21 hriplatin, a cisplatin derivative containing phenanthridine in place of one of the chloride ligands,

22 cular arylation to provide the corresponding phenanthridines in moderate to excellent yields.

23 Rotation about the Pt-N bond of the phenanthridine ligand racemizes the complex, and the que

24 iplatin because of the hydrophobicity of the phenanthridine ligand.

25 yliminyl radicals that proved convenient for phenanthridine preparations.

26 reaction, such as isoquinolines, quinoline, phenanthridine, quinazoline, phthalazine, and beta-carbo

27 n the formation of the antimicrobial benzo[c]phenanthridine sanguinarine and certain rhoeadine alkalo

28 ious route to the phenanthridine and benzo[c]phenanthridine skeletons.

29 Syntheses of phenanthridines starting from 2-formylbiphenyls were par

30 1-dihydroxy-5,6,6a,7,8,12b-hexahydrobenzo[a] phenanthridine], the first high-affinity full D1 agonist

31 ized and shown to generate the corresponding phenanthridines upon irradiation in the presence of 9,10

32 alideisoquinolines and antimicrobial benzo[c]phenanthridines were previously characterized.

33 r benzo-fused heterocycles (9H-carbazole and phenanthridine) when an aromatic amide anion is competit

34 xacyclic parnafungin C model decomposes to a phenanthridine with a half-life of 2 d in CDCl(3).

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