Ponesterone A

13408-56-5

CAS-Nr.: 13408-56-5

Englisch Name:: Ponesterone A

Synonyma:: PONASTERONE A;(2S,3R,5R,9R,10R,13R,14S,17S)-17-[(2R,3R)-2,3-dihydroxy-6-methylheptan-2-yl]-2,3,14-trihydroxy-10,13-dimethyl-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one;ponesterone A;25-DEOXYECDYSTERONE;Ponasterone A, >=98%;25-DEOXY-20-HYDROXYECDYSONE;Ponasterone A, Ecdysone analog;2B,3B,14A,20R,22R-PENTAHYDROXY-5B-CHOLEST-7-EN-6-ONE;2β,3β,14α,20r,22r-pentahydroxy-5β-cholest-7-en-6-one;(20R,22R)-2β,3β,14,20,22-Pentahydroxy-5β-cholesta-7-ene-6-one

CBNumber:: CB4155274

Summenformel:: C27H44O6

Molgewicht:: 464.63

MOL-Datei:: 13408-56-5.mol

Request For Quotation

Eigenschaften Sicherheit Verwendungswort Produktionsfirma 100

Ponesterone A Eigenschaften

Schmelzpunkt:: 259-260° (dec)

alpha: D15 +90° (methanol)

Siedepunkt:: 640.5±55.0 °C(Predicted)

Dichte: 1.22±0.1 g/cm3(Predicted)

storage temp.: −20°C

L?slichkeit: Methanol (Slightly, Sonicated), Pyridine (Slightly)

Aggregatzustand: White to off-white powder.

pka: 14.13±0.70(Predicted)

Farbe: White to Off-White

Biologische Quelle: synthetic (organic)

InChIKey: PJYYBCXMCWDUAZ-JJJZTNILSA-N

SMILES: C12=CC([C@]3([H])C[C@@H](O)[C@@H](O)C[C@]3(C)[C@@]1([H])CC[C@]1(C)[C@H](CC[C@@]21O)[C@](O)(C)[C@H](O)CCC(C)C)=O |&1:3,6,8,11,13,17,19,22,24,27,r|

CAS Datenbank: 13408-56-5(CAS DataBase Reference)

Sicherheit

WGK Germany	3
Speicherklasse	11 - Combustible Solids

Ponesterone A Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung

Ponesterone A, a steroidal compound, falls under the category of ecdysone and can be found in various sources throughout nature. It was first isolated from insect plants by Nakanishi and Horm in 1966. Compared to β-ecdysone, Ponesterone proves to be 3-100 times more potent in specific neurosensory systems.

Biochem/physiol Actions

Ponasterone A is an analogue of ecdysone. It induced death of non-adapted insects may be related to PoA regulating different set of genes when compared to 20E.

Ponesterone A Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte

Ponesterone A Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 100)Lieferanten

Firmenname	Telefon	E-Mail	Land	Produktkatalog	Edge Rate
TargetMol Chemicals Inc.	+1-781-999-5354; +17819995354	marketing@targetmol.com	United States	32466	58
Labnetwork lnc.	+86-27-50766799 +8618062016861	contact@labnetwork.com	China	19987	58
Henan Aochuang Chemical Co.,Ltd.	+86-0371-63689365 +8618638391208	sales@aochuangchem.com	China	9333	58
Aladdin Scientific		tp@aladdinsci.com	United States	57505	58
DAYANG CHEM (HANGZHOU) CO.,LTD	+86-88938639 +86-17705817739	info@dycnchem.com	China	53803	58
Mainchem Co., Ltd.	+86-0592-6210733	sale@mainchem.com	China	32343	55
Nanjing Peiwill Biotechnology Co.,Ltd.	025-57027729 15850702895	15850702895@163.com	China	89	55
J & K SCIENTIFIC LTD.	18210857532; 18210857532	jkinfo@jkchemical.com	China	96815	76
Chembest Research Laboratories Limited	021-20908456	sales@BioChemBest.com	China	6002	61
BioBioPha Co., Ltd.	0871-65217109 13211707573;	y.liu@mail.biobiopha.com	China	5645	65

2β,3β,14α,20r,22r-pentahydroxy-5β-cholest-7-en-6-one
2B,3B,14A,20R,22R-PENTAHYDROXY-5B-CHOLEST-7-EN-6-ONE
2BETA, 3BETA, 14ALPHA, 20R,22R-PENTAHYDROXY-5BETA-CHOLEST-7-EN-6-ONE
25-DEOXY-20-HYDROXYECDYSONE
25-DEOXYECDYSTERONE
Ponasterone A, >=98%
25-Deoxy-20-hydroxyecdysone, 25-Deoxyecdysterone, 2β,3β,14α,20R,22R-Pentahydroxy-5β-cholest-7-en-6-one
(20R,22R)-2β,3β,14,20,22-Pentahydroxy-5β-cholesta-7-ene-6-one
(20R,22R)-2β,3β,14α,20β,22α-Pentahydroxy-5β-cholesta-7-ene-6-one
Cholest-7-en-6-one, 2,3,14,20,22-pentahydroxy-, (2β,3β,5β,22R)-
gene,ecdysone,ecdysteroid,25-Deoxyecdysterone,expression,inhibit,Ponasterone A,Inhibitor
ponesterone A
Ponasterone A, Ecdysone analog
(2S,3R,5R,9R,10R,13R,14S,17S)-17-[(2R,3R)-2,3-dihydroxy-6-methylheptan-2-yl]-2,3,14-trihydroxy-10,13-dimethyl-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one
PONASTERONE A
13408-56-5
C27H44O6
Hormones
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Cytokines, Growth Factors and Hormones
Cell Biology
Cell Signaling and Neuroscience
BioChemical
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