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137071-32-0 分子结构
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(1R,9S,12S,13S,14S,17R,18Z,21S,23S,24R,25S,27R)-12-[(1E)-1-[(1R,3R,4S)-4-chloro-3-methoxycyclohexyl]prop-1-en-2-yl]-17-ethyl-1,14-dihydroxy-23,25-dimethoxy-13,19,21,27-tetramethyl-11,28-dioxa-4-azatricyclo[22.3.1.0^{4,9}]octacos-18-ene-2,3,10,16-tetrone

ChemBase编号:221
分子式:C43H68ClNO11
平均质量:810.45312
单一同位素质量:809.44808968
SMILES和InChIs

SMILES:
Cl[C@@H]1[C@H](OC)C[C@@H](CC1)/C=C(/[C@H]1OC(=O)[C@H]2N(C(=O)C(=O)[C@@]3(O[C@@H]([C@@H](OC)C[C@H]3C)[C@@H](OC)C[C@@H](C/C(=C\[C@@H](C(=O)C[C@@H](O)[C@@H]1C)CC)/C)C)O)CCCC2)\C
Canonical SMILES:
CC[C@H]1/C=C(/C)\C[C@@H](C)C[C@H](OC)[C@H]2O[C@](O)([C@@H](C[C@@H]2OC)C)C(=O)C(=O)N2[C@H](C(=O)O[C@@H]([C@H]([C@@H](CC1=O)O)C)/C(=C/[C@@H]1CC[C@@H]([C@@H](C1)OC)Cl)/C)CCCC2
InChI:
InChI=1S/C43H68ClNO11/c1-10-30-18-24(2)17-25(3)19-36(53-8)39-37(54-9)21-27(5)43(51,56-39)40(48)41(49)45-16-12-11-13-32(45)42(50)55-38(28(6)33(46)23-34(30)47)26(4)20-29-14-15-31(44)35(22-29)52-7/h18,20,25,27-33,35-39,46,51H,10-17,19,21-23H2,1-9H3/b24-18-,26-20+/t25-,27+,28-,29-,30+,31-,32-,33-,35+,36-,37-,38+,39+,43+/m0/s1
InChIKey:
KASDHRXLYQOAKZ-KDCWXYOMSA-N

引用这个纪录

CBID:221 http://www.chembase.cn/molecule-221.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
(1R,9S,12S,13S,14S,17R,18Z,21S,23S,24R,25S,27R)-12-[(1E)-1-[(1R,3R,4S)-4-chloro-3-methoxycyclohexyl]prop-1-en-2-yl]-17-ethyl-1,14-dihydroxy-23,25-dimethoxy-13,19,21,27-tetramethyl-11,28-dioxa-4-azatricyclo[22.3.1.0^{4,9}]octacos-18-ene-2,3,10,16-tetrone
IUPAC传统名
elidel
商标名
Elidel
别名
ASM 981
SDZ ASM 981
pimecrolimus
Pimecrolimus
CAS号
137071-32-0
PubChem SID
160963684
46505748
PubChem CID
17753757

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 DB00337 external link
PubChem 17753757 external link
数据来源 数据ID 价格

理论计算性质

理论计算性质

JChem ALOGPS 2.1
Acid pKa 9.955626  质子受体 10 
质子供体 LogD (pH = 5.5) 6.808116 
LogD (pH = 7.4) 6.806926  Log P 6.808131 
摩尔折射率 214.0262 cm3 极化性 84.57097 Å3
极化表面积 158.13 Å2 可自由旋转的化学键
里宾斯基五规则 false 
Log P 4.36  LOG S -5.73 
溶解度 1.52e-03 g/l 

分子性质

分子性质

理化性质 生物活性(PubChem)
疏水性(logP)
4.4 expand 查看数据来源

详细说明

详细说明

DrugBank DrugBank
DrugBank -  DB00337 external link
Item Information
Drug Groups approved; investigational
Description Pimecrolimus is an immunomodulating agent used in the treatment of atopic dermatitis (eczema). It is currently available as a topical cream, once marketed by Novartis, (however Galderma will be promoting the molecule in Canada in early 2007) under the trade name Elidel. [Wikipedia]
Indication For treatment of mild to moderate atopic dermatitis.
Pharmacology Pimecrolimus is a chemical that is used to treat atopic dermatitis (eczema). Atopic dermatitis is a skin condition characterized by redness, itching, scaling and inflammation of the skin. The cause of atopic dermatitis is not known; however, scientists believe that it may be due to activation of the immune system by various environmental or emotional triggers. Scientists do not know exactly how pimecrolimus reduces the manifestations of atopic dermatitis, but pimecrolimus reduces the action of T-cells and mast cells which are part of the immune system and contribute to responses of the immune system. Pimecrolimus prevents the activation of T-cells by blocking the effects of chemicals (cytokines) released by the body that stimulate T-cells. Pimecrolimus also reduces the ability of mast cells to release chemicals that promote inflammation.
Toxicity Side effects include burning sensation, irritation, pruritus, erythema, and skin infections, at the application site.
Affected Organisms
Humans and other mammals
Biotransformation No drug metabolism was observed in human skin in vitro. Oral administration yielded metabolites produced from O-demethylation and oxygenation reactions.
Absorption Because of the low systemic absorption of pimecrolimus following topical application the calculation of standard pharmacokinetic measures such as AUC, Cmax, half-life, etc. cannot be reliably done.
Protein Binding 74%-87% (in vitro, bound to plasma proteins)
Elimination 80% of the drug is excreted in the feces.
References
Grassberger M, Baumruker T, Enz A, Hiestand P, Hultsch T, Kalthoff F, Schuler W, Schulz M, Werner FJ, Winiski A, Wolff B, Zenke G: A novel anti-inflammatory drug, SDZ ASM 981, for the treatment of skin diseases: in vitro pharmacology. Br J Dermatol. 1999 Aug;141(2):264-73. [Pubmed]
External Links
Wikipedia
RxList
PDRhealth
Drugs.com

参考文献

参考文献

供应商提供 Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • Grassberger M, Baumruker T, Enz A, Hiestand P, Hultsch T, Kalthoff F, Schuler W, Schulz M, Werner FJ, Winiski A, Wolff B, Zenke G: A novel anti-inflammatory drug, SDZ ASM 981, for the treatment of skin diseases: in vitro pharmacology. Br J Dermatol. 1999 Aug;141(2):264-73. Pubmed
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专利

专利

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