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193901-90-5 分子结构
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gadolinium(3+) ion trisodium 2-{[1-({2-[bis(carboxylatomethyl)amino]ethyl}(carboxylatomethyl)amino)-3-[(4,4-diphenylcyclohexyl phosphonato)oxy]propan-2-yl](carboxylatomethyl)amino}acetate hydrate

ChemBase编号:4442
分子式:C33H40GdN3Na3O15P
平均质量:975.874871
单一同位素质量:976.11311507
SMILES和InChIs

SMILES:
C1CC(CCC1OP(=O)([O-])OCC(CN(CCN(CC(=O)[O-])CC(=O)[O-])CC(=O)[O-])N(CC(=O)[O-])CC(=O)[O-])(c1ccccc1)c1ccccc1.O.[Na+].[Na+].[Na+].[Gd+3]
Canonical SMILES:
[O-]C(=O)CN(C(CN(CC(=O)[O-])CCN(CC(=O)[O-])CC(=O)[O-])COP(=O)(OC1CCC(CC1)(c1ccccc1)c1ccccc1)[O-])CC(=O)[O-].O.[Na+].[Na+].[Na+].[Gd+3]
InChI:
InChI=1S/C33H44N3O14P.Gd.3Na.H2O/c37-28(38)18-34(15-16-35(19-29(39)40)20-30(41)42)17-26(36(21-31(43)44)22-32(45)46)23-49-51(47,48)50-27-11-13-33(14-12-27,24-7-3-1-4-8-24)25-9-5-2-6-10-25;;;;;/h1-10,26-27H,11-23H2,(H,37,38)(H,39,40)(H,41,42)(H,43,44)(H,45,46)(H,47,48);;;;;1H2/q;+3;3*+1;/p-6
InChIKey:
PIZALBORPSCYJU-UHFFFAOYSA-H

引用这个纪录

CBID:4442 http://www.chembase.cn/molecule-4442.html

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名称和登记号

名称和登记号

名称 登记号
IUPAC标准名
gadolinium(3+) ion trisodium 2-{[1-({2-[bis(carboxylatomethyl)amino]ethyl}(carboxylatomethyl)amino)-3-[(4,4-diphenylcyclohexyl phosphonato)oxy]propan-2-yl](carboxylatomethyl)amino}acetate hydrate
IUPAC传统名
gadolinium(3+) tripotassium 2-{[1-({2-[bis(carboxylatomethyl)amino]ethyl}(carboxylatomethyl)amino)-3-[(4,4-diphenylcyclohexyl phosphonato)oxy]propan-2-yl](carboxylatomethyl)amino}acetate hydrate
商标名
Vasovist
别名
Gadofosveset trisodium
CAS号
193901-90-5
PubChem SID
160967874
PubChem CID
23724913

数据来源

数据来源

所有数据来源 商品来源 非商品来源
数据来源 数据ID
DrugBank DB06705 external link
PubChem 23724913 external link
数据来源 数据ID 价格

理论计算性质

理论计算性质

JChem
Acid pKa 0.7821476  质子受体 15 
质子供体 LogD (pH = 5.5) -9.864648 
LogD (pH = 7.4) -16.179766  Log P -1.1778207 
摩尔折射率 241.5531 cm3 极化性 69.67652 Å3
极化表面积 268.96 Å2 可自由旋转的化学键 23 
里宾斯基五规则 false 

分子性质

分子性质

生物活性(PubChem)

详细说明

详细说明

DrugBank DrugBank
DrugBank -  DB06705 external link
Item Information
Drug Groups approved
Description Gadofosveset trisodium is an intravenous contrast agent used with magnetic resonance angiography(MRA), which is a non-invasive way of imaging blood vessels. The agent allows for the vascular system to be imaged more clearly by the MRA. In this way, gadofosveset trisodium is used to help diagnose certain disorders of the heart and blood vessels.
Indication Gadofosveset trisodium is used as a contrast agent in magnetic resonance angiography (MRA) to evaluate aortoiliac occlusive disease (AIOD) in adults with known or suspected peripheral vascular disease.
Pharmacology In human studies, gadofosveset substantially shortened blood T1 values for up to 4 hours after intravenous bolus injection. Relaxivity in plasma was measured to be 33.4 to 45.7 mM^-1s^-1 (0.47 T) over the dose range of up to 0.05 mmol/kg.
Toxicity Gadolinium-based contrast agents increase the risk for nephrogenic systemic fibrosis (NSF) in patients with acute or chronic severe renal insufficiency (glomerular filtration rate < 30 mL/min/1.73m2).
Affected Organisms
Humans and other mammals
Biotransformation Gadofosveset does not undergo measurable metabolism.
Half Life The mean half-life of the distribution phase is 0.48 ± 0.11 hours and the mean half-life of the elimination phase is 16.3 ± 2.6 hours.
Protein Binding At 0.05, 0.5, 1 and 4 hours after injection of 0.03 mmol/kg the plasma protein binding of gadofosveset ranges from 79.8 to 87.4%.
Elimination Gadofosveset is eliminated primarily in the urine with approximately 83.5% of an injected dose excreted in the urine over 14 days. Ninety-four percent (94%) of urinary excretion occurs in the first 72 hours. A small portion of gadofosveset dose is recovered in feces (approximately 4.7%).
Distribution 48 ± 16 mL/kg
Clearance 6.57 ± 0.97 mL/h/kg following the administration of 0.03 mmol/kg.
External Links
Wikipedia
Drugs.com

参考文献

参考文献

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专利

专利

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