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Synthesis and photochemical properties of psoralen derivatives = 소랄렌 유도체의 합성과 광화학적 특성
서명 / 저자 Synthesis and photochemical properties of psoralen derivatives = 소랄렌 유도체의 합성과 광화학적 특성 / Sung-Ki Kim.
발행사항 [대전 : 한국과학기술원, 2001].
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8012216

소장위치/청구기호

학술문화관(문화관) 보존서고

DCH 01008

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초록정보

A few psoralen derivatives $(Ps-O-C_3NH_2$, Ps-O-Glu, $Bis(C_4Ps)PIP$, $Bis(C_6Ps)PIP$, $Bis(C_8Ps)PIP)$ were synthesized and measured the photochemical and photobiological properties. The 5-substituent-8-methoxypsoralens $(-NO_2,-NH_2, -CH_2OH,-CHO,-CH_2OCH_3,-N(CH_3)_2,-Br)$ were synthesized to check the photophysical properties. All the experimental results were compared with those of 8-MOP which is widely used in clinics. The limiting factors in clinical use of photochemotherapeutic psoralens, 8-MOP, 5-MOP and TMP, are the poor water solubility and low intercalating efficiency with pyrimidine base pairs in DNA. Several psoralen derivatives $(Ps-O-C_3NH_2$, Ps-O-Glu, $Bis(C_4Ps)PIP$, $Bis(C_6Ps)PIP$, $Bis(C_8Ps)PIP)$, which are expected to have high reactivity and water solubility, were synthesized and investigated the solubility and photochemical inactivation of PCR by these compounds. $Ps-O-C_3NH_2$ and Ps-O-Glu have high water solubility than the widely used 8-MOP, however, these compounds did not prevent effectively the replication of DNA from PCR. The solubility of bispsoralen derivatives possessing two psoralens and one piperazine a molecule, 1,4-bis[n'-(8-psoralenoxy) alkyl] piperazine $(Bis(PsC_n)PIP n = 4,6,8)$ were comparable to that of 8-MOP but the piperazine-HCl salt formation of bispsoralens increased the solubility drastically. The relative binding constants of Bis(PsC_n)PIP (n = 4, 6, 8) to DNA were determined by the method of Hansen et al. The photo-crosslinking capacity of bispsoralens can be determined by using the non-renatured fraction (NRF). $Bis(PsC_n)$ PIP(n=4,6,8) shows the efficient intercalation into DNA, and good photo-crosslinking efficiency of DNA. $Bis(PsC_4)$PIP shows high lethality on bacteriophage T7 and can effectively inhibit the amplification of DNA by stopping the polymerase chain reactions in a short period of irradiation time. The order of hypochromism effect (% H) is in the order of Bis$(C_6Ps)PIP$ ≥ $Bis(C_4Ps PIP > Bis(C_8Ps)PIP$. %H decreased according to the increase of alkyl chain length connecting psoralens. $Bis(C_4Ps)PIP$ and $Bis(C_6Ps)PIP$ were intercalated more effectively than 8-MOP between pyrimidine base pairs in DNA. Some psoralen derivatives synthesized showed better inactivation of PCR reaction than 8-methoxypsoralen.

서지기타정보

서지기타정보
청구기호 {DCH 01008
형태사항 ix, 76 p. : 삽화 ; 26 cm
언어 영어
일반주기 저자명의 한글표기 : 김성기
지도교수의 영문표기 : Sang-Chul Shim
지도교수의 한글표기 : 심상철
수록잡지명 : "Photochemical and photobiological properties of new bispsoralen derivatives(Bis[PsCn]PIP, n=4,6,8)". Photochemistry and photobiology, v.72 no.4, pp.472-476 (2000)
학위논문 학위논문(박사) - 한국과학기술원 : 화학과,
서지주기 Reference : p. 69-76
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