Ajugasteron B

    WARNING: This product is for research use only, not for human or veterinary use.

Hodoodo CAT#: H592332

CAS#: 21490-21-1

Description: Ajugasteron B is a biochemical.


Chemical Structure

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Ajugasteron B
CAS# 21490-21-1

Theoretical Analysis

Hodoodo Cat#: H592332
Name: Ajugasteron B
CAS#: 21490-21-1
Chemical Formula: C29H46O7
Exact Mass: 506.32
Molecular Weight: 506.680
Elemental Analysis: C, 68.75; H, 9.15; O, 22.10

Price and Availability

This product is not in stock, which may be available by custom synthesis. For cost-effective reason, minimum order is 1g (price is usually high, lead time is 2~3 months, depending on the technical challenge). Quote less than 1g will not be provided. To request quote, please email to sales @hodoodo.com or click below button.
Note: Price will be listed if it is available in the future.

Request quote for custom synthesis

Synonym: Ajugasteron B

IUPAC/Chemical Name: 5beta,20xi,24xi-Stigmasta-7,25-dien-6-one, 2beta,3beta,14,20,22,27-hexahydroxy- Stigmasta-7,25-dien-6-one, 2,3,14,20,22,27-hexahydroxy-,

InChi Key: ODENAQIZHMFEAO-BQBPTSSQSA-N

InChi Code: InChI=1S/C29H46O7/c1-6-17(16(2)15-30)11-25(34)28(5,35)24-8-10-29(36)19-12-21(31)20-13-22(32)23(33)14-26(20,3)18(19)7-9-27(24,29)4/h12,17-18,20,22-25,30,32-36H,2,6-11,13-15H2,1,3-5H3/t17-,18+,20+,22-,23+,24+,25-,26-,27-,28-,29-/m1/s1

SMILES Code: CC[C@@H](C(CO)=C)C[C@@H](O)[C@@]([C@H]1CC[C@]2(O)[C@]1(C)CC[C@H]3C2=CC([C@H]4[C@]3(C)C[C@H](O)[C@H](O)C4)=O)(O)C

Appearance: Solid powder

Purity: >98% (or refer to the Certificate of Analysis)

Shipping Condition: Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.

Storage Condition: Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).

Solubility: Soluble in DMSO

Shelf Life: >3 years if stored properly

Drug Formulation: This drug may be formulated in DMSO

Stock Solution Storage: 0 - 4 C for short term (days to weeks), or -20 C for long term (months).

HS Tariff Code: 2934.99.03.00

More Info:

Biological target:
In vitro activity:
In vivo activity:

Preparing Stock Solutions

The following data is based on the product molecular weight 506.68 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
Formulation protocol:
In vitro protocol:
In vivo protocol:

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1: Xu H, Shi X, Ji X, Du Y, Zhu H, Zhang L. Qualitative and quantitative determination of nine main active constituents in Pulsatilla cernua by high-performance liquid chromatography coupled to electrospray ionization tandem mass spectrometry. J Sep Sci. 2011 Feb;34(3):308-16. doi: 10.1002/jssc.201000660. Epub 2011 Jan 3. PubMed PMID: 21268254.

2: Crouzet S, Maria A, Dinan L, Lafont R, Girault JP. Ecdysteroids from Cyanotis longifolia Benth. (Commelinaceae). Arch Insect Biochem Physiol. 2009 Dec;72(4):194-209. doi: 10.1002/arch.20329. PubMed PMID: 19760659.

3: Harmatha J, Vokác K, Kmonícková E, Zídek Z. Lack of interference of common phytoecdysteroids with production of nitric oxide by immune-activated mammalian macrophages. Steroids. 2008 Apr;73(4):466-71. doi: 10.1016/j.steroids.2007.12.014. Epub 2008 Feb 19. PubMed PMID: 18243265.

4: Budesínský M, Vokác K, Harmatha J, Cvacka J. Additional minor ecdysteroid components of Leuzea carthamoides. Steroids. 2008 May;73(5):502-14. doi: 10.1016/j.steroids.2007.12.021. Epub 2007 Dec 28. Erratum in: Steroids. 2009 Nov;74(12):1003-4. PubMed PMID: 18243263.

5: Coll J, Tandrón YA, Zeng X. New phytoecdysteroids from cultured plants of Ajuga nipponensis Makino. Steroids. 2007 Mar;72(3):270-7. Epub 2007 Jan 8. PubMed PMID: 17210166.

6: Santagati NA, Tropea S, Ronsisvalle G. Analysis of ecdysteroids by micellar electrokinetic chromatography with on-line preconcentration. J Chromatogr A. 2005 Jul 15;1081(1):77-86. PubMed PMID: 16013602.

7: Bourne PC, Whiting P, Dhadialla TS, Hormann RE, Girault JP, Harmatha J, Lafont R, Dinan L. Ecdysteroid 7,9(11)-dien-6-ones as potential photoaffinity labels for ecdysteroid binding proteins. J Insect Sci. 2002;2:11. PubMed PMID: 15455045; PubMed Central PMCID: PMC355911.

8: Suksamrarn A, Kumpun S, Yingyongnarongkul BE. Ecdysteroids of Vitex scabra stem bark. J Nat Prod. 2002 Nov;65(11):1690-2. PubMed PMID: 12444704.

9: Kholodova Y. Phytoecdysteroids: biological effects, application in agriculture and complementary medicine (as presented at the 14-th Ecdysone Workshop, July, 2000, Rapperswil, Switzerland). Ukr Biokhim Zh (1999). 2001 May-Jun;73(3):21-9. PubMed PMID: 12035548.

10: Tan CY, Wang JH, Zhang H, Li X. A new phytosterone from Cyanotis arachnoidea. J Asian Nat Prod Res. 2002 Mar;4(1):7-10. PubMed PMID: 11991195.

11: Odinokov VN, Galyautdinov IV, Nedopekin DV, Khalilov LM, Shashkov AS, Kachala VV, Dinan L, Lafont R. Phytoecdysteroids from the juice of Serratula coronata L. (Asteraceae). Insect Biochem Mol Biol. 2002 Feb;32(2):161-5. PubMed PMID: 11755058.

12: Cafieri F, Fattorusso E, Taglialatela-Scafati O. Novel bromopyrrole alkaloids from the sponge Agelas dispar. J Nat Prod. 1998 Jan;61(1):122-5. PubMed PMID: 9461661.