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3,4-ジクロロ-1H-2-ベンゾピラン-1-オン

3,4-Dichloroisocoumarin

HCID 1609
ノート反応
基本情報概要名称と識別子物性安全と法規制化学と産業関連反応化合物ノート
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基本情報

CAS
51050-59-0
標準SMILES
O=c1oc(Cl)c(Cl)c2ccccc12
InChIKey
SUGXUUGGLDCZKB-UHFFFAOYSA-N
分子式
C9H4Cl2O2
平均分子量
215.03 g/mol
単同位体質量
213.9588348

概要

3,4-dichloroisocoumarin is a member of the class of isocoumarins that is isocoumarin substituted by chloro groups at positions 3 and 4. It is a serine protease inhibitor. It has a role as a geroprotector and a serine protease inhibitor. It is an organochlorine compound and a member of isocoumarins.

名称と識別子

優先名称
3,4-Dichloroisocoumarin
IUPAC
3,4-dichloroisochromen-1-one
現地名
3,4-ジクロロ-1H-2-ベンゾピラン-1-オン
英語名
3,4-Dichloroisocoumarin
分子式
C9H4Cl2O2
分子量
215.03

名称と別名

3,4-dichloroisocoumarin51050-59-03,4-Dichloro-1H-isochromen-1-one3,4-Dcl3,4-Dichloro-1H-2-benzopyran-1-one1H-2-Benzopyran-1-one, 3,4-dichloro-SD08W1HH6EDTXSID70199056NSC-727363CHEBI:109540RefChem:91034DTXCID00121547
名称をさらに表示
3,4-ジクロロ-1H-2-ベンゾピラン-1-オン3,4-ジクロロイソクマリン3,4-ジクロロ-1H-2-ベンゾピラン1-オン3,4-ジクロロ-1H-イソクロメン-1-オン3,4-DICHLORO-2-BENZOPYRAN-1-ONE3,4 Dichloroisocoumarin, 10 mM in DMSO3,4-DCI, 3,4-Dichloro-2-benzopyran-1-one3,4-Dichloroisocoumarin - CAS 51050-59-0 - Calbiochem
637-085-43,4-dichloroisochromen-1-one3,4 dichloroisocoumarinMFCD000369603,4dichloroisocoumarinCHEMBL249833,4-DCISUGXUUGGLDCZKB-UHFFFAOYSA-N

データベース識別子

CAS
51050-59-0
PubChem CID
1609
DTXSID
DTXSID70199056

物性

構造計算による物性

XLogP
3.1
極性表面積
26.3 Ų
水素結合供与体数
0
水素結合受容体数
2
回転可能結合数
0
重原子数
13
形式電荷
0
複雑度
273

実験および物理化学的性質

DrugsPharmaceuticals -> Listed in ZINC15

物理化学的性質

沸点
304.7 · 304.7±42.0 °C(Predicted)
比重(密度)
1.53 · 1.53±0.1 g/cm3(Predicted)
貯蔵温度
2 · 2-8°C
溶解性
10 mMの濃度で可溶 · DMFまたはDMSOに10mMの濃度で可溶
外見
白色の凍結乾燥固体
色
White to off-white
BRN
6802625 · 6802625
InChI
1S/C9H4Cl2O2/c10-7-5-3-1-2-4-6(5)9(12)13-8(7)11/h1-4H
InChIKey
SUGXUUGGLDCZKB-UHFFFAOYSA-N
SMILES
ClC1=C(Cl)c2ccccc2C(=O)O1

安全と法規制

安全情報は参考情報です。供給元の安全データシート(SDS)、適用法令、専門家による評価に代わるものではありません。

GHS分類

GHS Classification · 4 件

Danger

H301 (100%): Toxic if swallowed [Danger Acute toxicity, oral]

P261, P264, P264+P265, P270, P271, P280, P301+P316, P302+P352, P304+P340, P305+P351+P338, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 38 reports by companies from 1 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

危険有害性情報

Hazard Classes and CategoriesAcute Tox. 3 (100%)

安全データ

wgk
3
ridadr
UN 2811 6.1/PG 3
risk_code
25-36/37/38
hazard_code
T
safety_code
26-36
hazard_class
6.1
Hazard Classifications
Acute Tox. 3 OralEye Irrit. 2Skin Irrit. 2STOT SE 3
ストレージクラス
6.1C - Combustible acute toxic Cat.3toxic compounds or compounds which causing chronic effects

化学と産業

薬理情報

MeSH Pharmacological ClassificationExogenous or endogenous compounds which inhibit SERINE ENDOPEPTIDASES.
応用分野 · 3 件

説明3,4-Dichloroisocoumarin (3,4-DCI) is a serine protease inhibitor. It completely inhibits enzyme activity of 24 serine proteases including human leukocyte elastase, thrombin, plasmin, Factor Xa, and Factor XIIa in vitro. 3,4-DCI stimulates caseinolytic activity of bovine pituitary multicatalytic proteinase complex (MPC) by inducing a conformational change in the MPC that exposes the caseinolytic active site. It has been used to functionally characterize the catalytic activities of multiple proteases including rat liver MPC and extracellular lipase.

使用Useful in a rapid staining method for identification of macrophages; counts by this method were confirmed by the more complex morphological criteria, by phagocytosis, and by the presence of Fc receptors. It is an inhibitor of Chymotrypsin and Trypsin. ,4 Dichloroisocoumarin also inhibits granzymes A, B, and H, cathepsin G, neutrophil elastase, proteinase and blocks apoptotic internucleosomal DNA cleavage in thymocytes without the involvement of endonucleases.

一般的な説明A potent irreversible inhibitor of serine proteases. Blocks apoptotic internucleosomal DNA cleavage in thymocytes without the involvement of endonucleases. Reacts with serine proteases to release an acylchloride moiety that can acylate another active site residue. Does not affect thiol proteases and metalloproteases. Also has no activity towards β-lactamases. Effective at concentrations ranging from 5-100 μM.

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関連反応

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化合物ノート

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CHEMBL24983
ChEBI
CHEBI:109540
UNII
SD08W1HH6E
EC Number
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