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50-24-8 分子结构
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(1S,2R,10S,11S,14R,15S,17S)-14,17-dihydroxy-14-(2-hydroxyacetyl)-2,15-dimethyltetracyclo[8.7.0.02,7.011,15]heptadeca-3,6-dien-5-one

ChemBase编号:738
分子式:C21H28O5
平均质量:360.44402
单一同位素质量:360.193674
SMILES和InChIs

SMILES:
O[C@]1([C@@]2([C@H]([C@H]3[C@H]([C@@H](O)C2)[C@@]2(C(=CC(=O)C=C2)CC3)C)CC1)C)C(=O)CO
Canonical SMILES:
OCC(=O)[C@@]1(O)CC[C@@H]2[C@]1(C)C[C@H](O)[C@H]1[C@H]2CCC2=CC(=O)C=C[C@]12C
InChI:
InChI=1S/C21H28O5/c1-19-7-5-13(23)9-12(19)3-4-14-15-6-8-21(26,17(25)11-22)20(15,2)10-16(24)18(14)19/h5,7,9,14-16,18,22,24,26H,3-4,6,8,10-11H2,1-2H3/t14-,15-,16-,18+,19-,20-,21-/m0/s1
InChIKey:
OIGNJSKKLXVSLS-VWUMJDOOSA-N

引用这个纪录

CBID:738 http://www.chembase.cn/molecule-738.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
(1S,2R,10S,11S,14R,15S,17S)-14,17-dihydroxy-14-(2-hydroxyacetyl)-2,15-dimethyltetracyclo[8.7.0.02,7.011,15]heptadeca-3,6-dien-5-one
(1S,2R,10S,11S,14R,15S,17S)-14,17-dihydroxy-14-(2-hydroxyacetyl)-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-3,6-dien-5-one
IUPAC传统名
prednisolone
(1S,2R,10S,11S,14R,15S,17S)-14,17-dihydroxy-14-(2-hydroxyacetyl)-2,15-dimethyltetracyclo[8.7.0.02,7.011,15]heptadeca-3,6-dien-5-one
商标名
Ak-Pred
Ak-Tate
Alphadrol
Articulose-50
Co-Hydeltra
Codelcortone
Cordrol
Cortalone
Cotogesic
Cotolone
Decaprednil
Decortin H
Delcortol
Delta F
Delta-Cortef
Delta-Stab
Deltacortenol
Deltacortril
Deltacortril Enteric
Deltasolone
Deltisilone
Depo-Medrol
Derpo Pd
Dexa-Cortidelt Hostacortin H
Di-Adreson F
Dicortol
Donisolone
Dydeltrone
Eazolin D
Econopred
Econopred Plus
Erbacort
Erbasona
Estilsona
Fernisolone
Fernisolone P
Fernisolone-P
Flamasone
Hostacortin H
Hydeltra
Hydeltra-Tba
Hydeltrasol
Hydeltrone
Hydrodeltalone
Hydrodeltisone
Hydroretrocortin
Hydroretrocortine
I-Pred
Inflamase Forte
Inflamase Mild
Key-Pred
Klismacort
Lentosone
Lite Pred
M-Predrol
Medrol
Medrol Acetate
Metacortandralone
Meti-Derm
Meticortelone
Metreton
Nisolone
Nor-Pred T.B.A.
Ocu-Pred
Ocu-Pred Forte
Ophtho-Tate
Orapred
Panafcortelone
Paracortol
Paracotol
Pediapred
Precortalon
Precortancyl
Precortilon
Precortisyl
Pred Forte
Pred Mild
Predair
Predair A
Predair Forte
Predalone 50
Predalone T.B.A.
Predate Tba
Predate-50
Predcor-25
Predcor-50
Predcor-Tba
Predne-Dome
Prednelan
Predni-Dome
Prednicen
Predniliderm
Predniretard
Prednis
Predonin
Predonine
Prelone
Prenolone
Rolisone
Scherisolon
Solone
Steran
Sterane
Sterolone
Supercortisol
Ulacort
Ultra Pred
Ultracorten H
Ultracortene H
Ultracortene-H
Ultracortene-Hydrogen
别名
1,4-孕甾二烯-11β,17α,21-三醇-3,20-二酮
1-去氢氢化可的松
1-去氢皮质醇
11β,17α,21-三羟基-1,4-孕甾二烯-3,20-二酮
泼尼松龙
11β, 17α, 21-Trihydroxypregna-1,4-diene-3,20-dione
1-Dehydrocortisol
1-Dehydrohydrocortisone
1,4-Pregnadiene-11β,17α,21-triol-3,20-dione
Prednisolone
(8S,9S,10R,11S,13S,14S,17R)-11,17-dihydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthren-3-one
1,4-Pregnadiene-11β,17α,21-triol-3,20-dione
11β,17α,21-Trihydroxy-1,4-pregnadiene-3,20-dione
PRDL
Deltahydrocortisone
Methylprednisolone Acetate
Predisolone Sodium Phosphate
Prednisolona [INN-Spanish]
Prednisolone Acetate
Prednisolone Sodium Phosphate
Prednisolone Tebutate
Prednisolonum [INN-Latin]
Prednisolone
Hydroretrocortine
Decaprednil
Predonine
Delta-Cortef
Hydeltra
(1S,2R,10S,11S,14R,15S,17S)-14,17-dihydroxy-14-(2-hydroxyacetyl)-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-3,6-dien-5-one
CAS号
50-24-8
EC号
200-021-7
MDL号
MFCD00003649
Beilstein号
1354103
PubChem SID
24898079
46504847
24870351
160964201
24898725
PubChem CID
5755

理论计算性质

理论计算性质

JChem ALOGPS 2.1
Acid pKa 12.584675  质子受体
质子供体 LogD (pH = 5.5) 1.2729899 
LogD (pH = 7.4) 1.2729871  Log P 1.2729899 
摩尔折射率 98.4933 cm3 极化性 38.038647 Å3
极化表面积 94.83 Å2 可自由旋转的化学键
里宾斯基五规则 true 
Log P 1.66  LOG S -3.18 
溶解度 2.39e-01 g/l 

分子性质

分子性质

理化性质 安全信息 药理学性质 产品相关信息 生物活性(PubChem)
溶解度
223 mg/L expand 查看数据来源
熔点
236 - 238°C expand 查看数据来源
240 °C (dec.)(lit.) expand 查看数据来源
decomposes 237-239 °C expand 查看数据来源
疏水性(logP)
1 expand 查看数据来源
1.423 expand 查看数据来源
保存条件
-20°C expand 查看数据来源
Room Temperature (15-30°C) expand 查看数据来源
RTECS编号
TU4152000 expand 查看数据来源
欧盟危险性物质标志
有害性(Harmful) 有害性(Harmful) (Xn) expand 查看数据来源
MSDS下载
下载链接 expand 查看数据来源
下载链接 expand 查看数据来源
下载链接 expand 查看数据来源
德国WGK号
3 expand 查看数据来源
危险公开号
22 expand 查看数据来源
GHS危险品标识
GHS07 expand 查看数据来源
GHS警示词
Warning expand 查看数据来源
GHS危险声明
H302 expand 查看数据来源
个人保护装置
dust mask type N95 (US), Eyeshields, Gloves expand 查看数据来源
相关基因信息
human ... AR(367), ESR1(2099), NR3C1(2908), NR3C2(4306), PGR(5241), SERPINA6(866)mouse ... Nr3c1(14815)rat ... Ar(24208) expand 查看数据来源
生物活性机理
Glucocorticoid receptor agonist. expand 查看数据来源
On binding, the corticoreceptor-ligand complex translocates itself into the cell nucleus, where it binds to many glucocorticoid response elements (GRE) in the promoter region of the target genes. expand 查看数据来源
The DNA bound receptor then interacts with basic transcription factors, causing an increase or decrease in expression of specific target genes, including suppression of IL2 (interleukin 2) expression. expand 查看数据来源
纯度
≥99% expand 查看数据来源
95% expand 查看数据来源
级别
analytical standard expand 查看数据来源
VETRANAL™, analytical standard expand 查看数据来源
成盐信息
Free Base expand 查看数据来源
质检报告
下载链接 expand 查看数据来源
包装
vial of 250 mg expand 查看数据来源
杂质
≤1.5 mol/mol water expand 查看数据来源
应用领域
Adrenergic agent expand 查看数据来源
Antiinflammatory agent expand 查看数据来源
Antineoplastic agent expand 查看数据来源
Pharmacopeia Traceability
traceable to BP 464 expand 查看数据来源
traceable to PhEur P2700000 expand 查看数据来源
traceable to USP 1555005 expand 查看数据来源
Empirical Formula (Hill Notation)
C21H28O5 expand 查看数据来源

详细说明

详细说明

MP Biomedicals MP Biomedicals DrugBank DrugBank Selleck Chemicals Selleck Chemicals Sigma Aldrich Sigma Aldrich
MP Biomedicals -  02102717 external link
Crystalline
DrugBank -  DB00860 external link
Item Information
Drug Groups approved
Description A glucocorticoid with the general properties of the corticosteroids. It is the drug of choice for all conditions in which routine systemic corticosteroid therapy is indicated, except adrenal deficiency states. [PubChem]
Indication For the treatment of primary or secondary adrenocortical insufficiency, such as congenital adrenal hyperplasia, thyroiditis. Also used to treat psoriatic arthritis, rheumatoid arthritis, ankylosing spondylitis, bursitis, acute gouty arthritis and epicondylitis. Also indicated for treatment of systemic lupus erythematosus, pemphigus and acute rhematic carditis. Can be used in the treatment of leukemias, lymphomas, thrombocytopenia purpura and autoimmune hemolytic anemia. Can be used to treat celiac disease, insulin resistance, ulcerative colitis and liver disorders.
Pharmacology Prednisolone is a synthetic glucocorticoid used as antiinflammatory or immunosuppressive agent. Prednisolone is indicated in the treatment of various conditions, including congenital adrenal hyperplasia, psoriatic arthritis, systemic lupus erythematosus, bullous dermatitis herpetiformis, seasonal or perennial allergic rhinitis, allergic corneal marginal ulcers, symptomatic sarcoidosis, idiopathic thrombocytopenic purpura in adults, leukemias and lymphomas in adults, and ulcerative colitis. Glucocorticoids are adrenocortical steroids and cause profound and varied metabolic effects. In addition, they modify the body's immune responses to diverse stimuli.
Toxicity LD50=500 mg/kg (oral, rat), short-term side effects include high blood glucose levels and fluid retention. Long term side effects include Cushing's syndrome, weight gain, osteoporosis, glaucoma, type II diabetes and adrenal suppression.
Affected Organisms
Humans and other mammals
Biotransformation Excreted in the urine as either free or glucoconjugate.
Absorption Readily absorbed by gastrointestinal tract, peak plasma concentration is reached 1-2 hours after administration.
Half Life 2-3 hours
Protein Binding Very high (>90%)
External Links
Wikipedia
RxList
Drugs.com
Selleck Chemicals -  S1737 external link
Research Area: Inflammation
Biological Activity:
Prednisolone(Hydroretrocortine) is a synthetic glucocorticoid with anti-inflammatory and immunomodulating properties. After cell surface receptor attachment and cell entry, prednisolone enters the nucleus where it binds to and activates specific nuclear receptors, resulting in an altered gene expression and inhibition of proinflammatory cytokine production. This agent also decreases the number of circulating lymphocytes, induces cell differentiation, and stimulates apoptosis in sensitive tumor cells populations. [1,2]
Sigma Aldrich -  P0152 external link
包装
Supplied in amber screw-cap vials
Sigma Aldrich -  P6004 external link
Analysis Note
Actual content given on label
Biochem/physiol Actions
Prednisolone is a glucocorticoid with anti-inflammatory and immunosuppressive activity.
包装
1, 5, 10, 25 g in poly bottle
100 mg in poly bottle
Sigma Aldrich -  46656 external link
法律信息
VETRANAL 商标 Sigma-Aldrich Co. LLC

参考文献

参考文献

供应商提供 Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • http://en.wikipedia.org/wiki/Prednisolone
  • Aldrich Library of 13C and 1H FT NMR Spectra, 1992, 3, 585B, (nmr)
  • Nobile, A. et al., J.A.C.S., 1955, 77, 4184, (biosynth)
  • Herzog, H.L. et al., Science (Washington, D.C.), 1955, 121, 176, (struct)
  • Zicha, L. et al., Arzneim.-Forsch., 1960, 10, 728; 831, (pharmacol, derivs)
  • Herzog, H.L. et al., Tetrahedron, 1962, 18, 581, (synth)
  • Hirschmann, R. et al., J.A.C.S., 1964, 86, 3903, (synth)
  • Toft, P. et al., Can. J. Spectrosc., 1970, 15, 137, (ms)
  • Gambertoglis, J.G. et al., J. Pharmacokinet. Biopharm., 1980, 8, 1, (rev, pharmacol)
  • Jusko, W.J. et al., Ther. Drug Monit., 1980, 2, 169, (rev, pharmacol)
  • Gonzalez, M.D. et al., Org. Magn. Reson., 1984, 22, 586, (cmr)
  • Negwer, M., Organic-Chemical Drugs and their Synonyms, 6th edn., Akademie-Verlag, 1987, 6297; 6321; 6941
  • Kirk, D.N. et al., J.C.S. Perkin 2, 1990, 1567, (pmr)
  • Ali, S.L., Anal. Profiles Drug Subst., 1992, 21, 415, (rev)
  • Martindale, The Extra Pharmacopoeia, 30th edn., Pharmaceutical Press, 1993, 737
  • Lewis, R.J., Sax's Dangerous Properties of Industrial Materials, 8th edn., Van Nostrand Reinhold, 1992, AAF625; PMA000; PMA100; SOV100; PLY300
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专利

专利

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