右旋安非他命

右旋安非他命
INN： Dexamfetamine
临床资料
AHFS/Drugs.com	Monograph
MedlinePlus	a605027
核准状况	美 FDA: Dextroamphetamine;
怀孕分级	澳: B3 ; ;
依赖性	生理依赖：无; 精神依赖：中
成瘾性	中
给药途径	口服
ATC码	N06BA02 (WHO) ;
法律规范状态
法律规范	澳：受管控（S8）; 加：Schedule I; 德：Anlage III; 英：Class B; 美：附表II;
药物动力学数据
生物利用度	Oral 75–100%
血浆蛋白结合率	15–40%
药物代谢	CYP2D6，多巴胺β羟化酶， FMO3（英语：Flavin-containing monooxygenase）
药效起始时间（英语：Onset of action）	IR服用：0.5至1.5小时; XR服用：1.5至2小时
生物半衰期	9至11小时; 不同的PH值：8至31小时
作用时间	IR服用：3至7小时; XR服用：12小时
排泄途径	肾（45%）；取决于尿液的pH值
识别信息
	IUPAC命名法 (2S)-1-phenylpropan-2-amine; ;
CAS号	51-64-9
PubChem CID	5826;
IUPHAR/BPS	2147;
DrugBank	DB01576 ;
ChemSpider	5621 ;
UNII	TZ47U051FI;
KEGG	D03740 ;
ChEBI	CHEBI:4469 ;
ChEMBL	ChEMBL612 ;
CompTox Dashboard（英语：CompTox Chemicals Dashboard） (EPA)	DTXSID8022907 ;
ECHA InfoCard	100.000.103
化学信息
化学式	C9H13N
摩尔质量	135.20622
3D模型（JSmol（英语：JSmol））	交互式图像;
密度	0.913 g/cm3
沸点	201.5 °C（394.7 °F）
水溶性	20 mg/mL (20 °C)
	SMILES C[C@@H](Cc1ccccc1)N;
	InChI InChI=InChI=1S/C9H13N/c1-8(10)7-9-5-3-2-4-6-9/h2-6,8H,7,10H2,1H3/t8-/m0/s1 ; Key:KWTSXDURSIMDCE-QMMMGPOBSA-N ;

右旋安非他命（英语：Dextroamphetamine）^{[注 1]}是强力中枢神经兴奋剂，也是苯丙胺（“安非他命”）的对映异构体，是注意力不足过动症（ADHD）和发作性嗜睡病的处方药。^[10]此外，它也被用作提升运动员能力的兴奋剂，也是一种益智药，同时人们在享乐时也将其用作春药和产生欣快感的药。此外，空军也将右旋安非他命广泛用作“抗睡丸”，在诸如夜间轰炸之类的容易疲倦的任务中使用。第二次世界大战期间，该药物也被用来治疗疲倦。

Quick Facts 临床资料, AHFS/Drugs.com ...

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[注 1]
其他英文名称：dexamphetamine （AAN（英语：Australian Approved Name））、dexamfetamine （国际非专利药品名称和BAN（英语：British Approved Name））、(S)-amphetamine、(+)-amphetamine、D-amphetamine。

[1]
Dextromphetamine. DrugBank. [2013-11-05]. （原始内容存档于2019-08-06）. |section=被忽略 (帮助)
[2]
Green-Hernandez, Carol; Singleton, Joanne K.; Aronzon, Daniel Z. Primary Care Pediatrics. Lippincott Williams & Wilkins. 2001-01-01: 243 [2017-05-07]. ISBN 9780781720083. （原始内容存档于2016-05-23）.|quote = Table 21.2 Medications for ADHD ... D-amphetamine ... Onset: 30 min.
[3]
Dexedrine, ProCentra(dextroamphetamine) dosing, indications, interactions, adverse effects, and more. reference.medscape.com. [2015-10-04]. （原始内容存档于2018-11-06）. Onset of action: 1–1.5 hr
[4]
Millichap JG. Chapter 9: Medications for ADHD. Millichap JG (编). Attention Deficit Hyperactivity Disorder Handbook: A Physician's Guide to ADHD 2nd. New York, USA: Springer. 2010: 112. ISBN 9781441913968.
Table 9.2 Dextroamphetamine formulations of stimulant medication
Dexedrine [Peak:2–3 h] [Duration:5–6 h] ...
Adderall [Peak:2–3 h] [Duration:5–7 h]
Dexedrine spansules [Peak:7–8 h] [Duration:12 h] ...
Adderall XR [Peak:7–8 h] [Duration:12 h]
Vyvanse [Peak:3–4 h] [Duration:12 h]
[5]
Brams M, Mao AR, Doyle RL. Onset of efficacy of long-acting psychostimulants in pediatric attention-deficit/hyperactivity disorder. Postgrad. Med. September 2008, 120 (3): 69–88. PMID 18824827. doi:10.3810/pgm.2008.09.1909. Onset of efficacy was earliest for d-MPH-ER at 0.5 hours, followed by d, l-MPH-LA at 1 to 2 hours, MCD at 1.5 hours, d, l-MPH-OR at 1 to 2 hours, MAS-XR at 1.5 to 2 hours, MTS at 2 hours, and LDX at approximately 2 hours. ... MAS-XR, and LDX have a long duration of action at 12 hours postdose
[6]
Adderall IR Prescribing Information (PDF). United States Food and Drug Administration. Teva Pharmaceuticals USA, Inc.: 1–6. October 2015 [2016-05-18]. （原始内容存档 (PDF)于2018-09-15）.
[7]
Mignot EJ. A practical guide to the therapy of narcolepsy and hypersomnia syndromes. Neurotherapeutics. October 2012, 9 (4): 739–752. PMC 3480574 . PMID 23065655. doi:10.1007/s13311-012-0150-9.
[8]
dextrostat (dextroamphetamine sulfate) tablet [Shire US Inc.]. DailyMed. Wayne, PA: Shire US Inc. August 2006 [2013-11-08]. （原始内容存档于2012-01-13）.
[9]
Lemke TL, Williams DA, Roche VF, Zito W. Foye's Principles of Medicinal Chemistry 7th. Philadelphia: Wolters Kluwer Health/Lippincott Williams & Wilkins. 2013: 648. ISBN 1609133455. Alternatively, direct oxidation of amphetamine by DA β-hydroxylase can afford norephedrine.
[10]
Dexedrine Prescribing Information (PDF). United States Food and Drug Administration. Amedra Pharmaceuticals LLC: 1–7. February 2015 [2015-09-04]. （原始内容存档 (PDF)于2017-02-17）.

[10] [注 1]
其他英文名称：dexamphetamine （AAN（英语：Australian Approved Name））、dexamfetamine （国际非专利药品名称和BAN（英语：British Approved Name））、(S)-amphetamine、(+)-amphetamine、D-amphetamine。

[1] [1]
Dextromphetamine. DrugBank. [2013-11-05]. （原始内容存档于2019-08-06）. |section=被忽略 (帮助)

[2] [2]
Green-Hernandez, Carol; Singleton, Joanne K.; Aronzon, Daniel Z. Primary Care Pediatrics. Lippincott Williams & Wilkins. 2001-01-01: 243 [2017-05-07]. ISBN 9780781720083. （原始内容存档于2016-05-23）.|quote = Table 21.2 Medications for ADHD ... D-amphetamine ... Onset: 30 min.

[3] [3]
Dexedrine, ProCentra(dextroamphetamine) dosing, indications, interactions, adverse effects, and more. reference.medscape.com. [2015-10-04]. （原始内容存档于2018-11-06）. Onset of action: 1–1.5 hr

[Millichap:_onset,_peak,_and_duration-4] [4]
Millichap JG. Chapter 9: Medications for ADHD. Millichap JG (编). Attention Deficit Hyperactivity Disorder Handbook: A Physician's Guide to ADHD 2nd. New York, USA: Springer. 2010: 112. ISBN 9781441913968.
Table 9.2 Dextroamphetamine formulations of stimulant medication
Dexedrine [Peak:2–3 h] [Duration:5–6 h] ...
Adderall [Peak:2–3 h] [Duration:5–7 h]
Dexedrine spansules [Peak:7–8 h] [Duration:12 h] ...
Adderall XR [Peak:7–8 h] [Duration:12 h]
Vyvanse [Peak:3–4 h] [Duration:12 h]

[XR_onset-duration-5] [5]
Brams M, Mao AR, Doyle RL. Onset of efficacy of long-acting psychostimulants in pediatric attention-deficit/hyperactivity disorder. Postgrad. Med. September 2008, 120 (3): 69–88. PMID 18824827. doi:10.3810/pgm.2008.09.1909. Onset of efficacy was earliest for d-MPH-ER at 0.5 hours, followed by d, l-MPH-LA at 1 to 2 hours, MCD at 1.5 hours, d, l-MPH-OR at 1 to 2 hours, MAS-XR at 1.5 to 2 hours, MTS at 2 hours, and LDX at approximately 2 hours. ... MAS-XR, and LDX have a long duration of action at 12 hours postdose

[Adderall_IR-6] [6]
Adderall IR Prescribing Information (PDF). United States Food and Drug Administration. Teva Pharmaceuticals USA, Inc.: 1–6. October 2015 [2016-05-18]. （原始内容存档 (PDF)于2018-09-15）.

[Narcolepsy_guide-7] [7]
Mignot EJ. A practical guide to the therapy of narcolepsy and hypersomnia syndromes. Neurotherapeutics. October 2012, 9 (4): 739–752. PMC 3480574 . PMID 23065655. doi:10.1007/s13311-012-0150-9.

[8] [8]
dextrostat (dextroamphetamine sulfate) tablet [Shire US Inc.]. DailyMed. Wayne, PA: Shire US Inc. August 2006 [2013-11-08]. （原始内容存档于2012-01-13）.

[DBH_ref-9] [9]
Lemke TL, Williams DA, Roche VF, Zito W. Foye's Principles of Medicinal Chemistry 7th. Philadelphia: Wolters Kluwer Health/Lippincott Williams & Wilkins. 2013: 648. ISBN 1609133455. Alternatively, direct oxidation of amphetamine by DA β-hydroxylase can afford norephedrine.

[Dexedrine-11] [10]
Dexedrine Prescribing Information (PDF). United States Food and Drug Administration. Amedra Pharmaceuticals LLC: 1–7. February 2015 [2015-09-04]. （原始内容存档 (PDF)于2017-02-17）.

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