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インカドロン酸二ナトリウム

Incadronic Acid

HCID 3699
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
124351-85-5
標準SMILES
O=P(O)(O)C(NC1CCCCCC1)P(=O)(O)O
InChIKey
LWRDQHOZTAOILO-UHFFFAOYSA-N
分子式
C8H19NO6P2
平均分子量
287.19 g/mol
単同位体質量
287.06876132

概要

Incadronic acid is a 1,1-bis(phosphonic acid).

名称と識別子

優先名称
Incadronic Acid
IUPAC
[(cycloheptylamino)-phosphonomethyl]phosphonic acid
現地名
インカドロン酸二ナトリウム
英語名
Incadronic
分子式
C8H19NO6P2
分子量
287.19

名称と別名

Incadronic acid124351-85-5((Cycloheptylamino)methylene)diphosphonic acidCimadronic acidIncadronic acid [INN]acido incadronicoacide incadroniqueNSC-723271UNII-G5C4M8847EG5C4M8847EIncadronic acid (INN)INCADRONIC ACID [MI]
名称をさらに表示
インカドロン酸二ナトリウムインカドロン酸Incadronic((cycloheptylamino)methylene)bis(phosphonic acid)[(cycloheptylamino)-phosphonomethyl]phosphonic acidPhosphonic acid, P,P'-[(cycloheptylamino)methylene]bis-
INCADRONIC ACID [MART.]INCADRONIC ACID [WHO-DD]DTXSID90154283[(cycloheptylamino)(phosphono)methyl]phosphonic acidNSC 723271INCADRONIC ACID (MART.)((cycloheptylamino)(phosphono)methyl)phosphonic acidacidum incadronicum

データベース識別子

CAS
124351-85-5
PubChem CID
3699
DTXSID
DTXSID90154283
ChEMBL
CHEMBL53950
ChEBI
CHEBI:135189

物性

構造計算による物性

XLogP
-3.5
極性表面積
127 Ų
水素結合供与体数
5
水素結合受容体数
7
回転可能結合数
4
重原子数
17
形式電荷
0
複雑度
307

実験および物理化学的性質

DrugsPharmaceuticals -> Listed in ZINC15

物理化学的性質

融点
232 · 232-233°
沸点
564.2 · 564.2±60.0 °C(Predicted)
比重(密度)
1.48 · 1.48±0.1 g/cm3(Predicted)
貯蔵温度
2 · 2-8°C
溶解性
Water (Slightly), Methanol (Slightly)
酸解離定数(Pka)
0.61 · 0.61±0.10(Predicted)
外見
Solid
色
White to Off-White

化学と産業

薬理情報

Mechanism of Action · 1 件

Bisphosphonates are taken into the bone where they bind to hydroxyapatite. Bone resorption by osteoclasts causes local acidification, releasing the bisphosphonate, which is taken into the osteoclast by fluid-phase endocytosis. Endocytic vesicles become acidified, releasing bisphosphonates into the cytosol of osteoclasts where they act. Osteoclasts mediate resorption of bone. When osteoclasts bind to bone they form podosomes, ring structures of F-actin. Disruption of the podosomes causes osteoclasts to detach from bones, preventing bone resorption. Nitrogen containing bisphosphonates such as incandronate are known to induce apoptosis of hematopoietic tumor cells by inhibiting the components of the mevalonate pathway farnesyl diphosphate synthase, farnesyl diphosphate, and geranylgeranyl diphosphate. These components are essential for post-translational prenylation of GTP-binding proteins like Rap1. The lack of prenylation of these proteins interferes with their function, and in the case of Rap1, leads to apoptosis. incadronate also activated caspases 3, 4, and 7; further contributing to apoptosis.

Biological Half-LifeIncadronate has a biexponential half life. The T<sub>1/2</sub>α is 0.26-0.40h and the T<sub>1/2</sub>β is 1.58-1.98h.
Metabolism/MetabolitesIncadronate is not metabolized in rats.
Absorption, Distribution and ExcretionIncadronate is 55.1-69.5% eliminated in the urine as the unchanged parent drug.
応用分野 · 2 件

説明Bisphonal, a new third generation drug, was launched in Japan for the treatment of osteoporosis. It can be prepared in two steps by heating cycloheptylamine, triethylorthoformate and diethyl phosphite followed by ester hydrolysis. The mechanism of action is not well understood. Bisphonal has no effect on bone mineralization but tightly binds to calcified bone matrix and inhibits bone resorption. It causes a decrease in the number and activity of osteoclasts (morphology and decrease in H+ secretion). They seem to undergo cell death with an impairment in the process of osteoclast formation. Bisphonal does not induce osteomalacia and its activity is partly mediated through osteoblasts (releases an inhibitor of osteoclast recruitment). It is a potent inhibitor of squalene synthase (50-fold) maybe by Mg2+ chelation or as a pyrophosphate mimic, undergoes practically no metabolism, and stimulates renal production of 1,25-dihydroxyvitamin D.

関連反応

3 件
反応記録を作成
HRID 1073687 の反応式
HRID 1073687生成物としてuspto-grants-1990_11
HRID 2107344 の反応式
HRID 2107344生成物としてuspto-grants-1990_06
HRID 2248551 の反応式
HRID 2248551生成物としてuspto-grants-1991_08

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
UNII
G5C4M8847E
Nikkaji
J615.831E

使用Incandronate is a bisphosphonate derivative. Bisphosphonates are most widely used as agents for treating osteoporosis and have also been used for other purposes such as herbicides, anticancer agents, and antiparasitics.

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