홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /화합물

P-113D

HCID 71587612
새 노트새 반응견적 요청하기
인쇄 미리보기
기본 정보개요이름 및 식별자물성화학 및 산업관련 반응화합물 노트
부분 구조 검색유사 구조 찾기

기본 정보

CAS
190673-60-0
표준 SMILES
C[C@@H](N)C(=O)N[C@H](CCCCN)C(=O)N[C@H](CCCNC(=N)N)C(=O)N[C@H](Cc1cnc[nH]1)C(=O)N[C@H](Cc1cnc[nH]1)C(=O)NCC(=O)N[C@H](Cc1ccc(O)cc1)C(=O)N[C@H](CCCCN)C(=O)N[C@H](CCCNC(=N)N)C(=O)N[C@H](CCCCN)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@H](Cc1cnc[nH]1)C(N)=O
InChIKey
UIBPZXXSPHGPDS-UXLZJAPBSA-N
분자식
C71H110N28O13
평균 분자량
1,563.8 g/mol
단동위원소 질량
1,562.88071568

개요

P-113D is a novel 12 amino-acid antimicrobial peptide drug derived from histatins, which are compounds found naturally in human saliva. It is being pursued as a potential treatment for cystic fibrosis by Demegen, Inc.

이름 및 식별자

우선 이름
P-113D
IUPAC
(2R)-6-amino-N-[(2R)-1-[[(2R)-1-[[(2R)-1-[[2-[[(2R)-1-[[(2R)-6-amino-1-[[(2R)-1-[[(2R)-6-amino-1-[[(2R)-1-[[(2R)-1-amino-3-(1H-imidazol-5-yl)-1-oxopropan-2-yl]amino]-1-oxo-3-phenylpropan-2-yl]amino]-1-oxohexan-2-yl]amino]-5-carbamimidamido-1-oxopentan-2-yl]amino]-1-oxohexan-2-yl]amino]-3-(4-hydroxyphenyl)-1-oxopropan-2-yl]amino]-2-oxoethyl]amino]-3-(1H-imidazol-5-yl)-1-oxopropan-2-yl]amino]-3-(1H-imidazol-5-yl)-1-oxopropan-2-yl]amino]-5-carbamimidamido-1-oxopentan-2-yl]-2-[[(2R)-2-aminopropanoyl]amino]hexanamide
영어명
P-113D
분자식
C71H110N28O13
분자량
1563.8129

이름 및 동의어

PulmadexP-113D513P3772TA190673-60-0DTXSID90172563RefChem:169272DTXCID9095054D-PEPTIDE OF THE SEQUENCE AKRHHGYKRKFH-NH2UNII-513P3772TAD-Peptide of the sequence akrhhgykrkfh - NH2348641-28-1orb2802021
이름 더 보기
SCHEMBL29366809EX-A15934TP2935CS-1181815Q27260856D-Alanyl-D-lysyl-D-arginyl-D-histidyl-D-histidylglycyl-D-tyrosyl-D-lysyl-D-arginyl-D-lysyl-D-phenylalanyl-D-histidinamide

데이터베이스 식별자

CAS
190673-60-0
PubChem CID
71587612
DTXSID
DTXSID90172563
UNII
513P3772TA

물성

구조 계산 물성

XLogP
-4.8
극성 표면적
697 Ų
수소 결합 공여자 수
26
수소 결합 수용자 수
22
회전 가능 결합 수
55
무거운 원자 수
112
형식 전하
0
복잡도
3,000

화학 및 산업

약리 정보

Pharmacodynamics · 1건

P-113D has demonstrated activity against CF patient clinical isolates of bacteria that are resistant to traditional antibiotics. The compound is stable and maintains activity in sputum of CF patients. P-113D was determined to be the smallest histatin fragment which retained antimicrobial activity equivalent to that of the parent compound. Interestingly, synthesizing P113 with D-amino acids gave rise P-113D, a compound that was impervious to enzymatic degradation and maintained the antimicrobial activity of the parent compound. P-113D also has very potent in vitro activity against a variety of Gram negative and positive bacteria including <i>P. aeruginosa</i>, <i>S. aureus</i>, <i>H. influenzae</i>, <i>S. typhimurium</i>, <i>E. coli</i>, <i>S. epidermidis</i>, <i>S. mutans</i> and <i>S. sobrinus</i>. In the case of <i>P. aeruginosa</i> and <i>S. aureus</i>, antibacterial activity has been demonstrated against a variety of CF patient clinical isolates which are resistant to traditional antibiotics. <i>P. aeruginosa</i> isolates that produce thick alginate secretions (mucoid phenotype) are also susceptible to killing by P-113D.

Mechanism of Action · 1건

For both bacteria and fungi such as <i>Candida albicans</i>, P-113D has been shown to kill cells as opposed to simply inhibiting their growth. It has been demonstrated that P-113D acts by binding to the cell surface and increasing the permeability of both the outer and inner membranes of the cells of Gram negative bacteria, killing them within seconds.

관련 반응

0건
반응 기록 만들기

현재 필터 조건에 해당하는 반응 기록이 없습니다.

화합물 노트

불러오는 중…

이 페이지에서기본 정보개요이름 및 식별자물성화학 및 산업관련 반응화합물 노트
더보기
새 노트새 반응견적 요청하기