ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
化工社オープンプロジェクト:[email protected]AIアクセス:llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.7.8
  1. ホーム
  2. /化合物

CID 6918992

HCID 6918992
ノート反応
基本情報概要名称と識別子物性化学と産業関連反応化合物ノート
部分構造検索類似構造を探す

基本情報

CAS
148-82-3
標準SMILES
[NH3+][C@@H](Cc1ccc(N(CCCl)CCCl)cc1)C(=O)[O-]
InChIKey
SGDBTWWWUNNDEQ-LBPRGKRZSA-N
分子式
C13H18Cl2N2O2
平均分子量
305.2 g/mol
単同位体質量
304.0745332

概要

Melphalan is a nitrogen mustard or bischloroethylamine type alkylating agent. It was first synthesized in the early 1950s by substituting L-phenylalanine for the methyl group on nitrogen mustard. Melphalan is used in the treatment of multiple myeloma and ovarian carcinoma. It is also used for high-conditioning before hematopoietic stem cell transplant. It is also used to treat uveal melanoma with unresectable hepatic metastases.

名称と識別子

優先名称
CID 6918992
IUPAC
(2S)-2-azaniumyl-3-[4-[bis(2-chloroethyl)amino]phenyl]propanoate

データベース識別子

CAS
148-82-3
PubChem CID
6918992

物性

構造計算による物性

XLogP
0.1
極性表面積
71 Ų
水素結合供与体数
1
水素結合受容体数
3
回転可能結合数
7
重原子数
19
形式電荷
0
複雑度
260

実験および物理化学的性質

LogP0.4
Solubility3.58e-01 g/L
Melting Point182.5 °C
Physical DescriptionSolid

化学と産業

薬理情報

Protein Binding · 1 件

Protein binding of melphalan ranges from 50% to 90%. Serum albumin is the major binding protein, accounting for approximately 40% to 60% of the plasma protein binding, while α1-acid glycoprotein accounts for about 20% of the plasma protein binding. Approximately 30% of melphalan is covalently and irreversibly bound to plasma proteins.

Pharmacodynamics · 1 件

Melphalan possesses cytotoxic, immunosuppressive, and myeloablative activities. Melphalan produces chromosomal aberrations _in vitro_ and _in vivo_; thus, it is considered to be potentially leukemogenic in humans. It also causes dose-limiting bone marrow suppression. The peak mean heart rate increased by 20 bpm from baseline following melphalan 100 mg/m<sup>2</sup> for two consecutive days in multiple myeloma patients undergoing autologous stem cell transplantation.

Mechanism of Action · 1 件

Melphalan is an alkylating agent of the bischloroethylamine type. It is believed to be taken up by tumour cells via a neutral amino acid active pathway shared by leucine. Melphalan binds at the N7 position of guanine and induces inter-strand cross-links in DNA, disrupting DNA synthesis or transcription. It can also cause DNA-protein cross-linking and induce lesions in RNA, proteins, and lipids. Melphalan is cytotoxic in resting and rapidly dividing tumour cells.

Biological Half-LifeIn patients given a single oral dose of 0.6 mg/kg of melphalan, the terminal elimination plasma half-life (± SD) was 1.5 ± 0.83 hours. Following intravenous administration, the terminal elimination half-life is approximately 75 minutes.
Metabolism/MetabolitesMelphalan primarily undergoes chemical hydrolysis to inactive metabolites, monohydroxymelphalan and dihydroxymelphalan. No other melphalan metabolites have been observed in humans.
Absorption, Distribution and Excretion · 4 件

The absorption of oral melphalan is highly variable concerning both the time to the first appearance of the drug in plasma (range: 0 to 6 hours) and peak plasma concentration (Cmax). The average absolute bioavailability of melphalan ranges from 56% to 93%. High variability in bioavailability may be due to incomplete intestinal absorption, variable first-pass hepatic metabolism, or rapid hydrolysis. Tmax was one hour in patients who received single oral doses of 0.2 mg/kg to 0.25 mg/kg of melphalan. Oral administration of melphalan with a high-fat meal may reduce melphalan exposure (AUC) by 36% to 54%. Mean (± SD) Cmax and AUC0-inf were 5.8 ± 1.5 mcg/mL and 451 ± 109 mcg x min/mL, respectively, following intravenous administration of 100 mg/m2 in multiple myeloma patients.

関連反応

0 件
反応記録を作成

現在のフィルター条件では反応記録がありません。

化合物ノート

読み込み中…

このページの内容基本情報概要名称と識別子物性化学と産業関連反応化合物ノート

About 5.8% to 21.3% of melphalan is excreted in urine.

The volume of distribution of melphalan ranges from approximately 35.5 to 185.7 L/m<sup>2</sup>. Penetration into cerebrospinal fluid is low.

Average total body clearance (CL) ranges from approximately 250 to 325 mL/min/m<sup>2</sup>.

Cellular LocationsCytoplasm