InChI key
KBAUFVUYFNWQFM-UHFFFAOYSA-N
InChI
1S/C17H22N2O.C4H6O4/c1-17(20-14-13-19(2)3,15-9-5-4-6-10-15)16-11-7-8-12-18-16;5-3(6)1-2-4(7)8/h4-12H,13-14H2,1-3H3;1-2H2,(H,5,6)(H,7,8)
SMILES string
OC(=O)CCC(O)=O.CN(C)CCOC(C)(c1ccccc1)c2ccccn2
form
powder
originator
Sanofi Aventis
Quality Level
Gene Information
human ... HRH1(3269)
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Application
琥珀酸多西拉敏已被用于研究在CS培养基低视黄酸浓度的情况下，非致畸性暴露（non-teratogenic exposures ）对人胚胎干细胞聚集体（HESCA）-CSR的形态和基因表达的影响。
琥珀酸多西拉敏盐已被用作检查发育毒性的治疗药物。
Biochem/physiol Actions
H 1 组胺受体拮抗剂；催眠药。
多西拉敏抑制组胺 H1 受体。它与失眠的短期管理和普通感冒症状的暂时缓解有关。另一方面，多西拉敏中毒与横纹肌溶解和继发性急性肾功能衰竭有关。
对小鼠的研究显示，多西拉敏诱导肝微粒体细胞色素 P450 和其它与甲状腺素 (T4) 代谢有关的酶。本药与盐酸吡哆醇合用，可治疗晨吐。
多西拉敏抑制组胺 H1 受体。它与失眠的短期管理和普通感冒症状的暂时缓解有关。另一方面，多西拉敏中毒与横纹肌溶解和继发性急性肾功能衰竭有关。
对小鼠的研究显示，多西拉敏诱导肝微粒体细胞色素 P450 和其它与甲状腺素 (T4) 代谢有关的酶。本药与盐酸吡哆醇合用，可治疗晨吐。
General description
多西拉敏属于乙醇胺类抗组胺药，经肝脏代谢为 N -去甲基多西拉敏和 N , N -二去甲基多西拉敏。 它通常是一种非处方药 (OTC)，用于治疗过敏和感冒症状。
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 2
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
D V Gauvin et al.
European journal of pharmacology, 294(1), 281-288 (1995-12-27)
Rats were trained to discriminate between 10 mg/kg cocaine and saline injections under a fixed ratio 10 schedule of food-motivated lever press responding. Once stimulus control was achieved, reinforced test sessions were conducted to assess the degree of generalization of
L J Brandes et al.
Journal of the National Cancer Institute, 86(10), 770-775 (1994-05-18)
Present studies of drug-induced tumor growth promotion have evolved from earlier investigations into the mechanism of action of N,N-diethyl-2-[4-(phenylmethyl)phenoxy[ethanamine.HCl, a tamoxifen derivative which potently inhibits lymphocyte mitogenesis in vitro and stimulates tumor growth in vivo. It is thought that potency
Development and validation of method for simultaneous estimation of pyridoxine hydrochloride and doxylamine succinate in tablet dosage form by first order derivative spectroscopy.
Nataraj KS
International Journal of Pharmacy and Pharmaceutical Sciences, 5 (2013)
Irena Nulman et al.
The Canadian journal of clinical pharmacology = Journal canadien de pharmacologie clinique, 16(3), e400-e406 (2009-11-20)
The delayed-release combination of doxylamine succinate and pyridoxine hydrochloride was the most commonly used antiemetic (Bendectin) approved by FDA for nausea and vomiting of pregnancy (NVP) until its removal of the market in 1983. The drug is widely used today
H Mizoguchi et al.
International journal of clinical pharmacology and therapeutics, 45(4), 230-236 (2007-05-04)
The aim of this study was to evaluate the efficacy of a single night-time dose of a syrup containing paracetamol, dextromethorphan hydrobromide, doxylamine succinate and ephedrine sulfate in subjects with multiple cold symptoms. A syrup containing 15 mg dextromethorphan hydrobromide
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