基本情報
- CAS
85650-56-2- 標準SMILES
CN1C[C@@H]2c3ccccc3Oc3ccc(Cl)cc3[C@H]2C1.O=C(O)/C=C\C(=O)O- InChIKey
GMDCDXMAFMEDAG-CHHFXETESA-N- 分子式
- C21H20ClNO5
- 平均分子量
- 401.8 g/mol
- 単同位体質量
- 401.10300042
概要
(S,S)-asenapine maleate is a maleate salt obtained by combining equimolar amounts of (S,S)-asenapine and maleic acid. It contains a (S,S)-asenapine(1+). It is an enantiomer of a (R,R)-asenapine maleate.
名称と識別子
- 優先名称
- Asenapine Maleate
- IUPAC
- (Z)-but-2-enedioic acid;(2S,6S)-9-chloro-4-methyl-13-oxa-4-azatetracyclo[12.4.0.02,6.07,12]octadeca-1(18),7(12),8,10,14,16-hexaene
- 現地名
- アセナピンマレイン酸塩
- 英語名
- Asenapine Maleate
- 分子式
- C17H16ClNO.C4H4O4
- 分子量
- 401.84
名称と別名
名称をさらに表示
データベース識別子
- CAS
85650-56-2- PubChem CID
- 6917875
- DTXSID
DTXSID301017360- ChEMBL
CHEMBL3544974- ChEBI
CHEBI:71248- UNII
- CU9463U2E2
- EC Number
- 288-064-8
物性
構造計算による物性
- 極性表面積
- 87.1 Ų
- 水素結合供与体数
- 2
- 水素結合受容体数
- 6
- 回転可能結合数
- 2
- 重原子数
- 28
- 形式電荷
- 0
- 複雑度
- 482
実験および物理化学的性質
Human Drugs
Breast Feeding; Lactation; Milk, Human; Antipsychotic Agents
FDA approved drugs -> Active ingredient
EMA approved medicines: Human medicine
FDA approved drugs -> Active ingredient
物理化学的性質
- 融点
- 141 · 141-145°
- 闪点
- 9 ℃ · 9℃
- 貯蔵温度
- 2 · 2-8°C
- 溶解性
- 2 O: · H2O: ≥10mg/mL
- 酸解離定数(Pka)
- 1 · pK1 <3, pK2 7.52, pK3 8.51(at 25℃)
- 外見
- 粉
- 色
- ホワイトからオフホワイト
- 水溶解度
- 6.25 mg/mL · Water : 6.25 mg/mL (15.55 mM; Need ultrasonic and warming)
- InChIKey
- GMDCDXMAFMEDAG-CHHFXETESA-N
- SMILES
- C(/C(=O)O)=C/C(=O)O.CN1C[C@]2([H])C3C=CC=CC=3OC3C=CC(Cl)=CC=3[C@@]2([H])C1 |&1:11,27,r|
化学的性質
化学的特性White Solid
安全と法規制
GHS分類
GHS Classification
Danger
H301 (98.4%): Toxic if swallowed [Danger Acute toxicity, oral]
P203, P260, P261, P264, P264+P265, P270, P271, P273, P280, P284, P301+P316, P302+P352, P304+P340, P305+P351+P338, P316, P318, P319, P320, P321, P330, P332+P317, P337+P317, P362+P364, P391, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 63 reports by companies from 9 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
危険有害性情報
毒性情報
安全データ
- wgk
- 3
- ridadr
- UN1230 - class 3 - PG 2 - Methanol, solution
- hs_code
- 29339900
- risk_code
- 22-36/37/38-50/53-39/23/24/25-23/24/25-11
- hazard_code
- Xn,N,T,F
- safety_code
- 26-60-61-45-36/37-16
- Hazard Classifications
- Acute Tox. 3 OralAquatic Acute 1Eye 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
FDA Pharmacological Classification
ASENAPINE MALEATE
Atypical Antipsychotic [EPC]
MeSH Pharmacological Classification
Agents that control agitated psychotic behavior, alleviate acute psychotic states, reduce psychotic symptoms, and exert a quieting effect. They are used in SCHIZOPHRENIA; senile dementia; transient psychosis following surgery; or MYOCARDIAL INFARCTION; etc. These drugs are often referred to as neuroleptics alluding to the tendency to produce neurological side effects, but not all antipsychotics are likely to produce such effects. Many of these drugs may also be effective against nausea, emesis, and pruritus.
応用分野
説明Asenapine, a dual antagonist of dopamine D2and serotonin 5-HT2receptors, was launched for the acute treatment of schizophreniaand manic or mixed episodes associated with bipolar I disorder in adults. Asenapine exhibits high affinity for serotonin 5-HT1A, 5-HT1B, 5-HT2A, 5-HT2B, 5-HT2C, 5-HT5, 5-HT6, and 5-HT7 receptors (Ki = 2.5, 4.0, 0.06, 0.16, 0.03, 1.6, 0.25, and 0.13 nM, respectively); dopamine D1, D2, D3, and D4 receptors (Ki = 1.4, 0.42, 1.1, and 1.3 nM, respectively); a1- and a2-adrenergic receptors (Ki = 1.2 and 1.2 nM, respectively); and histamine H1 receptors (Ki = 1.0 nM), and moderate affinity for H2 receptors (Ki = 6.2 nM). In in vitro assays, asenapine acts as an antagonist at these receptors. Asenapine has no appreciable affinity for muscarinic cholinergic receptors (e.g., Ki = 8128 nM for M1). Despite its potent binding affinity for multiple receptors, the efficacy of asenapine in schizophrenia is thought to be primarily mediated through a combination of antagonist activity at D2 and 5-HT2A receptors.
使用Asenapine Maleate is a 5-HT receptor antagonist developed for the treatment of acute schizophrenia and bipolar mania.
一般的な説明Asenapine is a new atypical antipsychotic developed for the treatment of schizophrenia and acute mania associated with bipolar disorder. The drug is marketed under the trade names Saphris and Sycrest. This certified solution standard is suitable for LC/MS or GC/MS applications in clinical toxicology, forensic testing, or pharmaceutical research.
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