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틱소코르톨

Tixocortol

HCID 162955
노트반응

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기본 정보개요이름 및 식별자물성화학 및 산업관련 반응화합물 노트
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기본 정보

CAS
61951-99-3
표준 SMILES
C[C@]12CCC(=O)C=C1CC[C@@H]1[C@@H]2[C@@H](O)C[C@@]2(C)[C@H]1CC[C@]2(O)C(=O)CS
InChIKey
YWDBSCORAARPPF-VWUMJDOOSA-N
분자식
C21H30O4S
평균 분자량
378.5 g/mol
단동위원소 질량
378.18648044

개요

Tixocortol is a steroid sulfide in which the sulfanyl group is at C-21 of a polyoxygenated derivative of pregn-4-ene. It has a role as a glucocorticoid receptor agonist. It is a tertiary alpha-hydroxy ketone, a 17alpha-hydroxy steroid, an 11beta-hydroxy steroid, a 20-oxo steroid, a 3-oxo-Delta(4) steroid and a steroid sulfide. It derives from a hydride of a pregnane.

이름 및 식별자

우선 이름
Tixocortol
IUPAC
(8S,9S,10R,11S,13S,14S,17R)-11,17-dihydroxy-10,13-dimethyl-17-(2-sulfanylacetyl)-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-3-one
현지명
틱소코르톨
영어명
Tixocortol
분자식
C21H30O4S
분자량
378.53

이름 및 동의어

Tixocortol61951-99-3TixocortolumZX3KEK657Z11beta,17-dihydroxy-21-sulfanylpregn-4-ene-3,20-dioneCHEBI:63560DTXSID30895062Pregn-4-ene-3,20-dione, 11,17-dihydroxy-21-mercapto-, (11beta)-RefChem:190184A07EA05R01AD07DTXCID101324618
이름 더 보기
틱소코르톨Cortisol 21-Thiol11β,17-Dihydroxy-21-Mercaptoprogesterone(11β)-11,17-Dihydroxy-21-Mercaptopregn-4-ene-3,20-dionePregn-4-ene-3,20-dione, 11,17-dihydroxy-21-mercapto-, (11β)-
612-814-9Tixocortol (INN)(1R,3aS,3bS,9aR,9bS,10S,11aS)-1,10-dihydroxy-9a,11a-dimethyl-1-(2-sulfanylacetyl)-1H,2H,3H,3aH,3bH,4H,5H,7H,8H,9H,9aH,9bH,10H,11H,11aH-cyclopenta[a]phenanthren-7-one(8S,9S,10R,11S,13S,14S,17R)-11,17-dihydroxy-10,13-dimethyl-17-(2-sulfanylacetyl)-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-3-one(11beta)-11,17-dihydroxy-21-mercaptopregn-4-ene-3,20-dioneTIXOCORTOL [INN]Tixocortol [INN:BAN]Tixocortolum [INN-Latin]

데이터베이스 식별자

CAS
61951-99-3

물성

구조 계산 물성보충 중

XLogP
2
극성 표면적
75.6 Ų
수소 결합 공여자 수
3
수소 결합 수용자 수
5
회전 가능 결합 수
2
무거운 원자 수
26
형식 전하
0
복잡도
687

실험 및 물리화학적 성질

DrugsPharmaceuticals -> Listed in ZINC15
SolubilityInsoluble
Endocrine DisruptorsPotential endocrine disrupting compound
Boiling Point607ºC at 760 mmHg
Melting Point50-55ºC

물리화학적 성질

녹는점
254 °C · 254 °C (decomp)
끓는 점
559.31 · 559.310±50.00 °C(Press: 760.00 Torr)(predicted)
밀도
1.27 · 1.270±0.10 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted)
산도 계수 (pKa)
7.916 · 7.916±0.10(predicted)

화학 및 산업

약리 정보

ATC Code · 4건

R - Respiratory system

A - Alimentary tract and metabolism

QR - Respiratory system

QA - Alimentary tract and metabolism

Protein BindingThe presence of the C-17 in the corticosteroids is a protein binding site.
Pharmacodynamics · 1건

Tixocortol presents the characteristic of local action which reduces significantly the side effects of systemic glucocorticoids. Reports have demonstrated that gastrointestinal administration of tixocortol generates a decrease in abdominal pain, bleeding, and frequency of stools which resulted in an amelioration in the malabsorption laboratory tests. All the effects were independent of suppression of the pituitary-adrenal axis, which was shown by the absence of significant depression of cortisol. Administration of tixocortol as a nasal spray has been shown to respect nasal drainage by the ciliary beats of the pituitary mucosa. The actions of tixocortol have no effect on leukocyte count, blood glucose level, sodium urinary excretion, and immunosupressive activity on lymphocytes.

Mechanism of Action · 1건

The mechanism of action of tixocortol is similar to other corticosteroids regarding the binding sites and prostaglandin synthesis but the local properties of tixocortol are given by the immediate liver metabolism and transformation withing red blood cells. All the immediate transformations of tixocortol classified it as part of the nonsystemic steroids.

Biological Half-LifeTixocortol presents a shorter half-life than cortisol.
Metabolism/Metabolites · 1건

Tixocortol is rapidly modified within red blood cells and it is immediately metabolized by a first-pass liver metabolism. The metabolites of tixocortol are mainly represented by the formation of sulfo- and glucurono-conjugates which are later hydrolyzed from the conjugate forming neutral steroids. The metabolic transformations are the reduction of the 3-keto and delta 4 system, reduction of the C-20 carbonyl group, oxidation of the C-11 alcohol and cleavage of the side chain at C-17. The specific metabolic pathways of the C-21 thiol ester function were its transformation into methylthio, methylsulfonyl and methylsulfonyl derivatives and reductive cleavage of the C-21-S bond leading to 21-methyl structures. None of the metabolites have affinity for glucocorticoid receptors. This and the extensive metabolism explains the exclusive local activities of tixocortol.

관련 반응

1건
반응 기록 만들기
HRID 1196827 반응식
HRID 1196827반응물로uspto-grants-1992_05

화합물 노트

불러오는 중…

이 페이지에서기본 정보개요이름 및 식별자물성화학 및 산업관련 반응화합물 노트
PubChem CID
162955
DTXSID
DTXSID30895062
ChEBI
CHEBI:63560
UNII
ZX3KEK657Z
EC Number
612-814-9
Nikkaji
J18.528K
Absorption, Distribution and Excretion · 4건

The absorption of tixocortol is the same as in other steroids including hydrocortisone. Oral administration of tixocortol presents a 10-20% bioavailability with a significantly lower plasma Cmax than cortisol. The fast metabolism, larger volume of distribution and low bioavailability donates tixocortol with the absence of systemic activity.

Tixocortol has a rapid elimination after continuous metabolism. Urine analysis of oral administration of tixocortol demonstrate a complete lack of unchanged drug.

Studies have shown that oral or intravenous administration of tixocortol presents a significantly larger volume of distribution compared to cortisol of 21.7 L/kg.

Studies have shown that oral or intravenous administration of tixocortol presents a significantly larger clearance rate compared to cortisol of 33.3 L h/kg.

응용 분야

용도Tixocortol is an anti-inflammatory agent. Tixocortol is used in fluorescent chemoaffinity labeling.

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공급사5 곳

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추가 설명

정의ChEBI: A steroid sulfide in which the sulfanyl group is at C-21 of a polyoxygenated derivative of pregn-4-ene.