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아크리바스틴

(E)-3-[6-[(E)-1-(4-methylphenyl)-3-pyrrolidin-1-ium-1-ylprop-1-enyl]-2-pyridinyl]prop-2-enoate

HCID 40466858
노트반응
기본 정보개요이름 및 식별자물성안전 및 규제화학 및 산업관련 반응화합물 노트
부분 구조 검색유사 구조 찾기

기본 정보

CAS
87848-99-5
표준 SMILES
Cc1ccc(/C(=C\C[NH+]2CCCC2)c2cccc(/C=C/C(=O)[O-])n2)cc1
InChIKey
PWACSDKDOHSSQD-IUTFFREVSA-N
분자식
C22H24N2O2
평균 분자량
348.4 g/mol
단동위원소 질량
348.18377801

개요

Acrivastine is a triprolidine analog antihistamine indicated for the treatment of allergies and hay fever. As an H1 receptor antagonist, it functions by blocking the action of histamine at this receptor thereby preventing the symptoms associated with histamine release such as pruritis, vasodilation, hypotension, edema, bronchoconstriction, and tachycardia. Acrivastine is currently available in combination with pseudoephedrine as the FDA-approved product Semprex-D.

이름 및 식별자

우선 이름
(E)-3-[6-[(E)-1-(4-methylphenyl)-3-pyrrolidin-1-ium-1-ylprop-1-enyl]-2-pyridinyl]prop-2-enoate
IUPAC
(E)-3-[6-[(E)-1-(4-methylphenyl)-3-pyrrolidin-1-ium-1-ylprop-1-enyl]-2-pyridinyl]prop-2-enoate
현지명
아크리바스틴
영어명
Acrivastine
분자식
C22H24N2O2
분자량
348.44

이름 및 동의어

아크리바스틴(E)-3-(6-((E)-3-(Pyrrolidin-1-yl)-1-(p-tolyl)prop-1-en-1-yl)pyridin-2-yl)acrylic acidSemprexBW-825CBW-270CBW-A825CAcrivastinACRIVASTINEAcrivastine>Acrivastine/BW825CAcrivastine USP/EP/BP

데이터베이스 식별자

CAS
87848-99-5
PubChem CID
40466858

물성

구조 계산 물성

XLogP
2.3
극성 표면적
57.5 Ų
수소 결합 공여자 수
1
수소 결합 수용자 수
3
회전 가능 결합 수
5
무거운 원자 수
26
형식 전하
0
복잡도
509

물리화학적 성질

녹는점
222 ° · 222° (dec)
끓는 점
555.1 · 555.1±50.0 °C(Predicted)
밀도
1.17 · 1.170±0.06 g/cm3(Predicted)
저장 조건
2 · 2-8°C
용해도
2 mg/mL · DMSO: >2mg/mL(가온)
물리적 상태
가루
산도 계수 (pKa)
1.99 · 1.99±0.10(Predicted)
색상
흰색에서 베이지색
안정성
감광성
InChI
InChI=1S/C22H24N2O2/c1-17-7-9-18(10-8-17)20(13-16-24-14-2-3-15-24)21-6-4-5-19(23-21)11-12-22(25)26/h4-13H,2-3,14-16H2,1H3,(H,25,26)/b12-11+,20-13+
InChIKey
PWACSDKDOHSSQD-IUTFFREVSA-N
SMILES
C(O)(=O)/C=C/C1=NC(/C(/C2=CC=C(C)C=C2)=C/CN2CCCC2)=CC=C1

안전 및 규제

안전 정보는 참고용이며, 공급업체의 물질안전보건자료(SDS), 관련 법규 및 전문가 평가를 대체하지 않습니다.

안전 데이터

wgk
3
rtecs
UD3474000
스토리지 클래스
11 - Combustible Solids

화학 및 산업

약리 정보

Protein BindingAcrivastine binding to human plasma proteins was 50 ± 2.0%.
Biological Half-LifeThe mean terminal half-life for acrivastine was 1.9 ± 0.3 hours following single oral doses and increased to 3.5 ± 1.9 hours at steady state. The terminal half-life for the propionic acid metabolite was 3.8 ± 1.4 hours.
Absorption, Distribution and Excretion · 4건

Acrivastine was absorbed rapidly from the combination capsule following oral administration and was as bioavailable as a solution of acrivastine. After administration of SEMPREX-D Capsules, maximum plasma acrivastine concentrations were achieved at 1.14 ± 0.23 hour.

A mass balance study in 7 healthy volunteers showed that acrivastine is primarily eliminated by the kidneys. Over a 72-hour collection period, about 84% of the administered total radioactivity was recovered in urine and about 13% in feces, for a combined recovery of about 97%.

0.46 ± 0.05 L/kg

2.9 ± 0.7 mL/min/kg

Metabolite PathwaysAcrivastine H1-Antihistamine Action
응용 분야 · 3건

개요Acrivastine is an orally-active HI .receptor antagonist reportedly useful in the treatment of allergic rhinitis. The main advantages of acrivastine in comparison to older antihistamines are its low sedative potential and the absence of anticholinergic side-effects.

용도Acrivastine has been used as an antihistamine to investigate the relation between the increased residence time of antihistamine at the histamine H1 receptor (H1R) and the duration of effective target-inhibition by this antagonist.

일반 설명Acrivastine, (E, E)-3-[6-[1-(4-methylphenyl)-3-(1-pyrrolidinyl)-1-propenyl-2-pyridinyl]-2-propenoic acid(Semprex), is a fixed-combination product of the antihistamineacrivastine (8 mg) with the decongestant pseudoephedrine(60 mg). Acrivastine is an odorless, white to pale cream crystallinepowder that is soluble in chloroform and alcohol andslightly soluble in water.Acrivastine is an analog of triprolidine containing acarboxyethenyl moiety at the 6-position of the pyridylring. Acrivastine shows antihistaminic potency and durationof action comparable to those of triprolidine (Table23.2). Unlike triprolidine, acrivastine does not display significantanticholinergic activity at therapeutic concentrations.Also, the enhanced polarity of this compound resultingfrom carboxyethenyl substitution limits BBBaccumulation, and thus, this compound produces less sedationthan triprolidine.Limited pharmacokinetic data are available for this compound.Orally administered drug has a half-life of about 1.7hours and a total body clearance of 4.4 mL/min per kilogram.The mean peak plasma concentrations are reported tovary widely, and the drug appears to penetrate the CNSpoorly. The metabolic fate of acrivastine has not beenreported.

상·하류 제품 정보

상류 원료

2,6-Dibromopyridine피롤Bromidep-Tolunitrile트리페닐포스핀암모니아(가스)탄산나트륨(경회)부틸리튬황산수산화나트륨염산디에틸포스포노아세트산에틸에스테르2,6-Dibromopyridin-3-amineP-톨루엔설폰 산수소화나트륨

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추가 설명 · 1건

정의ChEBI: A member of the class of pyridines that is (pyridin-2-yl)acrylic acid substituted at position 6 by a [(1E)-1-(4-methylphenyl)-3-(pyrrolidin-1-yl)prop-1-en-1-yl group. It is a non-sedating antihistamine used for treatment of hayfever, urtic ria, and rhinitis.

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