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Stigmastadienone is a naturally occurring plant steroid, specifically a diterpenoid, which has been found to possess various biological activities. It is derived from the Croton tonkinensis plant and has been the subject of research for its potential applications in the field of medicine.

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  • (8S,9S,10R,13R,14S,17R)-17-[(E,2S,5S)-5-ethyl-6-methyl-hept-3-en-2-yl]-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one

    Cas No: 20817-72-5

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  • 20817-72-5 Structure
  • Basic information

    1. Product Name: STIGMASTADIENONE
    2. Synonyms: (22E)-Stigmasta-4,22-dien-3-one;4,22-Stigmastadiene-3-one;crytalline;Stigmasta-4,22-dien-3-one;4,22-Cholestadien-24-ethyl-3-one;24-Ethyl-4,22E-cholestadien-3-one;(8S,9S,10R,13R,14S,17R)-17-[(E,2R,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one
    3. CAS NO:20817-72-5
    4. Molecular Formula: C29H46O
    5. Molecular Weight: 410.67494
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 20817-72-5.mol
  • Chemical Properties

    1. Melting Point: 123-127 °C
    2. Boiling Point: 503.2°Cat760mmHg
    3. Flash Point: 262.3°C
    4. Appearance: /
    5. Density: 0.98g/cm3
    6. Vapor Pressure: 2.97E-10mmHg at 25°C
    7. Refractive Index: 1.525
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: STIGMASTADIENONE(CAS DataBase Reference)
    11. NIST Chemistry Reference: STIGMASTADIENONE(20817-72-5)
    12. EPA Substance Registry System: STIGMASTADIENONE(20817-72-5)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 20817-72-5(Hazardous Substances Data)

20817-72-5 Usage

Uses

Used in Pharmaceutical Industry:
Stigmastadienone is used as a starting material for the synthesis of various pharmaceutical compounds, particularly those with anti-inflammatory properties. Its ability to modulate biological processes makes it a valuable asset in the development of new drugs.
Used in Biological Studies:
Stigmastadienone is used as a key compound in the isolation and characterization of anti-inflammatory diterpenoids from Croton tonkinensis. This application aids in the discovery and understanding of novel bioactive compounds with potential therapeutic benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 20817-72-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,8,1 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 20817-72:
(7*2)+(6*0)+(5*8)+(4*1)+(3*7)+(2*7)+(1*2)=95
95 % 10 = 5
So 20817-72-5 is a valid CAS Registry Number.
InChI:InChI=1/C29H46O/c1-7-21(19(2)3)9-8-20(4)25-12-13-26-24-11-10-22-18-23(30)14-16-28(22,5)27(24)15-17-29(25,26)6/h8-9,18-21,24-27H,7,10-17H2,1-6H3/b9-8+/t20?,21-,24?,25?,26?,27?,28+,29-/m1/s1

20817-72-5Relevant articles and documents

Ruthenium-catalyzed Oppenauer-type oxidation of 3β-hydroxy steroids. A highly efficient entry into the steroidal hormones with 4-en-3-one functionality

Almeida, Maria L. S.,Kocǒvsky, Pavel,Báckvall, Jan-E?.

, p. 6587 - 6590 (1996)

Oxidation of 5-unsaturated 3β-hydroxy steroids 1 to the corresponding 4-en-3-one derivatives 2 can be performed efficiently by acetone at reflux in the presence of a catalytic system consisting of either (PPh3)3RuCl2 (3) and K2CO3 or [(C4Ph4COHOCC4Ph4)(μ-H)][(CO)4Ru2] (4). The reaction proceeds via a ruthenium-catalyzed dehydrogenation of 1 and subsequent hydrogen transfer to acetone with concomitant double bond migration.

Cytotoxic effect of some pentacyclic triterpenes and hemisynthetic derivatives of stigmasterol

Sandjo, Louis P.,Rincheval, Vincent,Ngadjui, Bonaventure T.,Kirsch, Gilbert

, p. 731 - 734 (2011)

Two different oxidation reactions (PCC and KMnO4) of stigmasterol gave three products, stigmasta-4,22-dien-3-one (1a), stigmasta-4,22-diene-3,6-dione (1b), and 3-O-acetyl-5β,6β- epoxystigmast-22-ene-3-ol (1c). The cytotoxic activities of hemisynthetic compounds, stigmasterol, and four pentacyclic triterpens 2-5 previously isolated from cultivated and wild Triumfetta cordifolia and identified were investigated against human fibrosarcoma cell line (HT1080). Most of the drugs showed moderate cytotoxic activity. It was also notice that the triterpene skeleton had a range of number of OH functions in which activity was observed. Spectroscopic analyses (1H and 13C NMR) and mass were used to elucidate the structure of hemisynthetic compounds.

Structure and synthesis of a progesterone homologue from the skin of the dorid nudibranch Aldisa smaragdina

Gavagnin, Margherita,Ungur, Nicon,Mollo, Ernesto,Templado, Jose,Cimino, Guido

, p. 1500 - 1504 (2002)

The short-side-chain steroid 24-norchol-4-ene-3,22-done (6) has been found to be the main metabolite of both skin and mucus of the mollusc Aldisa smaragdina. This compound, previously reported as a microbial degradation product of cholesterol, has never previously been isolated from natural sources. The absolute stereochemistry was determined by synthesis from commercial stigmasterol, and a full NMR characterisation is also reported. Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002.

Microbial transformation of β-sitosterol and stigmasterol into 26-oxygenated derivatives

Ambrus, Gabor

, p. 621 - 625 (1995)

The genetically modified Mycobacterium sp. BCS 396 strain has been used to transform sterols with stigmastane side chain in order to obtain 26-oxidized metabolites. β-Sitosterol (I) was transformed to 4-stigmasten-3-one (II), 26-hydroxy-4-stigmasten-3-one (III), and 3-oxo-4-stigmasten-26-oic acid (IV), while stigmasterol (V) was converted to 4,22-stigmastadien-3-one (VI), 6β-hydroxy-4,22-stigmastadien-3-one (VII), 26-hydroxy-4,22-stigmastadien-3-one (VIII), 3-oxo-4,22-stigmastadien-26-oic acid methyl ester (IX), and 3-oxo-1,4,22-stigmastatrien-26-oic acid methyl ester (X) with that strain. In both β-sitosterol and stigmasterol, 26-oxidation generates the R-configuration on C-25.

Synthesis and search for 3β,3′β-disteryl ethers after high-temperature treatment of sterol-rich samples

Bus, Katarzyna,Ofiara, Karol,Sitkowski, Jerzy,Szterk, Arkadiusz,Zmys?owski, Adam

, (2020/06/08)

It has been proven that at increased temperature, sterols can undergo various chemical reactions e.g., oxidation, dehydrogenation, dehydration and polymerisation. The objectives of this study are to prove the existence of dimers and to quantitatively analyse the dimers (3β,3′β-disteryl ethers). Sterol-rich samples were heated at 180 °C, 200 °C and 220 °C for 1 to 5 h. Quantitative analyses of the 3β,3′β-disteryl ethers were conducted using liquid extraction, solid-phase extraction and gas chromatography coupled with mass spectrometry. Additionally, for the analyses, suitable standards were synthetized from native sterols. To identify the mechanism of 3β,3′β-disteryl ether formation at high temperatures, an attempt was made to use the proposed synthesis method. Additionally, due to the association of sterols and sterol derivatives with atherosclerosis, preliminary studies with synthetized 3β,3′β-disteryl ethers on endothelial cells were conducted.

Base-free oxidation of alcohols enabled by nickel(ii)-catalyzed transfer dehydrogenation

Ye, Danfeng,Liu, Zhiyuan,Sessler, Jonathan L.,Lei, Chuanhu

supporting information, p. 11811 - 11814 (2020/10/13)

An efficient nickel(ii)-catalyzed transfer dehydrogenation oxidation of alcohols is reported that relies on cyclohexanone as the formal oxidant and does not require the use of an external base. The synthetic utility of this protocol is demonstratedviathe facile oxidation of structurally complicated natural products.

Antiangiogenic brassinosteroid compounds

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Page/Page column 7, (2015/12/04)

A method of treating a solid tumor in a mammal by inhibiting angiogenesis, including administering to the mammal which has a solid tumor selected from the group consisting of breast carcinoma, lung carcinoma, prostate carcinoma, colon carcinoma, ovarian carcinoma, neuroblastoma, central nervous system tumor, multiform glioblastoma and melanoma; a composition including brassinosteroids of general formula (I) wherein can be a single or double bond and the configurations of carbon atoms C22 and C23 respectively linked to the substituents HO are S for both carbon atoms and a pharmaceutically acceptable additive.

Pincer and diamine Ru and Os diphosphane complexes as efficient catalysts for the dehydrogenation of alcohols to ketones

Baratta, Walter,Bossi, Gianluca,Putignano, Elisabetta,Rigo, Pierluigi

experimental part, p. 3474 - 3481 (2011/05/02)

The ruthenium and osmium complexes [MCl2(diphosphane)(L)] (M=Ru, Os; L=bidentate amino ligand) and [MCl(CNN)(dppb)] (CNN=pincer ligand; dppb=1,4-bis- (diphenylphosphino)butane), containing the N-H moiety, have been found to catalyze the acceptorless dehydrogenation of alcohols in tBuOH and in the presence of KOtBu. The compounds trans-[MCl2(dppf)(en)] (M=Ru 7, Os 13; dppf=1,1′-bis(diphenylphosphino)ferrocene; en=ethylenediamine) display very high activity and different substrates, including cyclic and linear alcohols, are efficiently oxidized to ketones by using 0.8-0.04mol% of catalyst. The effect of the base and the comparison of the catalytic activity of the Ru versus Os complexes are reported. The ruthenium complex 7 generally leads to a faster conversion into ketones with respect to the osmium complex 13, which displays better activity in the dehydrogenation of 5-en-3β-hydroxy steroids. The synthesis of new Ru and Os complexes [MCl2(PP)(L)] (PP=dppb, dppf; L=(±)-trans-1,2-diaminocyclohexane, 2-(aminomethyl) pyridine, and 2-aminoethanol) of trans and cis configuration is also reported. Alcohol breakdown: Ruthenium and osmium phosphane complexes containing nitrogen ligands with the N-H functionality efficiently catalyze the acceptorless dehydrogenation of alcohols. With [MCl2(dppf)(en)] (M=Ru, Os; dppf=1,1′-bis(diphenylphosphino)ferrocene; en=ethylenediamine) in the presence of KOtBu several alcohols have been converted into ketones (see scheme), including sterols for which Os displays a better activity than Ru. Copyright

Quantitative structure inter-activity relationship (QSInAR). Cytotoxicity study of some hemisynthetic and isolated natural steroids and precursors on human fibrosarcoma cells HT1080

Putz, Mihai V.,Lazea, Marius,Sandjo, Louis P.

scheme or table, p. 6603 - 6620 (2011/11/12)

Combined experimental and quantitative structure inter-activity relationship (QSIAR) computation methods were advanced in order to establish the structural and mechanistic influences that steroids and triterpenes, either as newly synthesized or naturally isolated products, have on human HT1080 mammalian cancer cells. The main Hansch structural indicators such as hydrophobicity (LogP), polarizability (POL) and total energy (Etot) were considered and both the structure-projected as well as globally computed correlations were reported; while the inter-activity correlation of the global activity with those projected on structural information was revealed as equal to the direct structural-activity one for the trial sets of compounds, the prediction for the testing set of molecules reported even superior performances respecting those characteristic for the calibration set, validating therefore the present QSInAR models; accordingly, it follows that the LogP carries the most part of the cytotoxic signal, while POL has little influence on inhibiting tumor growth-A complementary behavior with their earlier known influence on genotoxic carcinogenesis. Regarding the newly hemisynthetic compounds it was found that stigmasta-4,22-dien-3-one is not adapted for cell membrane diffusion; it is recommended that aminocinnamyl chlorohydrate be further modified in order to acquire better steric influence, while aminocinnamyl-2,3,4,6-O- tetraacetyl-a-D-glucopyranoside was identified as being inhibited in the tumor cell by other molecular mechanisms-here not revealed-although it has a moderate-high anti-cancer structurally predicted activity.

COMPOUND SHOWING ANTI-INFLAMMATORY ACTIVITY AND ANTIVIRAL ACTIVITY, PHARMACEUTICAL COMPOSITIONS COMPRISING THE SAME, A PROCESS FOR OBTAINING THE SAME AND USE OF THE SAME IN THE TREATMENT OF EPIDEMIC KERATOCONJUNCTIVITES AND HERPETIC STROMAL KERATIS

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Page/Page column 4, (2010/06/11)

The present invention refers to a compound having anti-inflammatory and antiviral activity according to the following structural formula: wherein, R1 and R3 are selected from H, HO—, R5—O—, HCOO—, R5—COO—, —OOC—R6—COO—, p-toluene sulphonate, phosphate, tartrate, maleate, sulphate, fluorine, chlorine, bromine, iodine and methanesulphonate,R2 is selected from H, HO—, R5—O—, HCOO—, R5—COO—, —OOC—R6—COO—, p-toluene sulphonate, phosphate, tartrate, maleate, sulphate, fluorine, chlorine, bromine, and iodine,or —R1 and —R2 can be together —O—, (CH3)2—(CO)2-(ó-(CH3—CH2)2—(CO)2—R4 and R5 are selected from H and linear or branched C1-C4 alkyl,R6 is —(CH2)n equals to 1, 2 ó 3, and, can be a single bond or double bond, to the pharmaceutical compositions comprising the same, to a process for preparing the same and to the use of the same for preparing pharmaceutical compositions. Particularly, the compounds of the invention are particularly useful for preparing ophthalmic pharmaceuticals for the treatment of diseases caused by adenovirus and preferably, epidemic keratoconjunctivitis. Also, the compounds of the invention are particularly useful for preparing ophthalmic pharmaceuticals for the treatment of diseases caused by the herpes simplex type 1 (HSV-1) and preferably, herpetic stromal keratitis (HK).

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