Skip to Content
MilliporeSigma

Skip To

SML2395

Sigma-Aldrich

Elocalcitol

≥98% (HPLC)

Synonym(s):

(1R,3Z,5S)-3-[(2E)-2-[(3aS,7aS)-1-[(1S,3E)-5-ethyl-5-hydroxy-1-methyl-3-hepten-1-yl]-3,3a,5,6,7,7a-hexahydro-7a-methyl-4H-inden-4-ylidene]ethylidene]-5-fluoro-4-methylenecyclohexanol, BXL 628, BXL-628, Ro 26-9228

Sign Into View Organizational & Contract Pricing

Select a Size

Change View
5 G
MYR 395.00

About This Item

Empirical Formula (Hill Notation):
C29H43FO2
CAS Number:
Molecular Weight:
442.65
MDL number:
UNSPSC Code:
12352200

MYR 395.00


Check Cart for Availability

Request a Bulk Order
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Assay

≥98% (HPLC)

form

powder

optical activity

[α]/D +97 to +107°, c = c=1 in methanol

color

white to beige

solubility

DMSO: 2 mg/mL, clear

storage temp.

−20°C

SMILES string

F[C@H]1C[C@@H](C\C(=C\C=C2\[C@H]3[C@](CCC\2)(C(=CC3)[C@H](C\C=C\C(O)(CC)CC)C)C)\C1=C)O

InChI

1S/C29H43FO2/c1-6-29(32,7-2)17-8-10-20(3)25-14-15-26-22(11-9-16-28(25,26)5)12-13-23-18-24(31)19-27(30)21(23)4/h8,12-14,17,20,24,26-27,31-32H,4,6-7,9-11,15-16,18-19H2,1-3,5H3/b17-8+,22-12+,23-13-/t20-,24+,26-,27-,28+/m0/s1

InChI key

LRLWXBHFPGSUOX-GJQYOBCGSA-N

Compare Similar Items

View Full Comparison

Show Differences

1 of 4

This Item
L4385L5385L6010
biological source

bovine milk

biological source

bovine milk

biological source

bovine milk

biological source

bovine milk

technique(s)

electrophoresis: suitable

technique(s)

microbiological culture: suitable

technique(s)

cell culture | mammalian: suitable, electrophoresis: suitable

technique(s)

indirect ELISA: suitable

Quality Level

200

Quality Level

200

Quality Level

300

Quality Level

300

form

powder

form

lyophilized powder

form

lyophilized powder

form

lyophilized powder

Gene Information

cow ... LALBA(281894)

Gene Information

cow ... LALBA(281894)

Gene Information

cow ... LALBA(281894)

Gene Information

cow ... LALBA(281894)

storage temp.

2-8°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

Biochem/physiol Actions

Elocalcitol (BX-L628) is an analog of Vitamin D3 that acts as an agonist at vitamin D VDR receptors. It has been shown to inhibit prostate cell growth and RhoA/Rho-kinase signaling. Elocalcitol (BXL-628) downregulated the expression of active RhoA and ROCK activity induced by high glucose and was shown to have renal protective effects.
Elocalcitol is a Vitamin D receptor (VDR) agonist and is an analog of calcitriol.[1][2] Elocalcitol possesses anti-inflammatory and anti- proliferative properties.[1] It regulates cell apoptosis and cell proliferation by binding to Vitamin D receptors (VDR).[3] It shows a therapeutic effect on people suffering from Benign prostatic hyperplasia (BPH) and lower urinary tract symptoms (LUTS).[2]
Vitamin D3 analog

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our Documents section.

If you need assistance, please contact Customer Support

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Yee Voan Teo et al.
Cell reports, 27(4), 997-1007 (2019-04-25)
Oncogene-induced senescence (OIS) is a tumor suppressive response to oncogene activation that can be transmitted to neighboring cells through secreted factors of the senescence-associated secretory phenotype (SASP). Currently, primary and secondary senescent cells are not considered functionally distinct endpoints. Using
Chiral mono and diamide derivatives of calix [4] arene for enantiomeric recognition of chiral amines
Kocabas, Erdal, et al.
Chirality, 20.1, 26-34 (2008)
Isoindolinones via a room temperature palladium nanoparticle-catalysed 3-component cyclative carbonylation?amination cascade
Grigg, Ronald, et al.
Tetrahedron, 44.37, 6979-6982 (2003)
Expedient synthesis and design strategies for new peptoid construction
Gorske, Benjamin C., et al.
Organic Letters, 7.8, 1521-1524 (2005)
Synthesis of optically-active planar chiral derivatives of ferrocene. Crystal structures of alkyne insertion products.
Zhao G, et al.
Tetrahedron Asymmetry, 9(13), 2253-2257 (1998)

Articles

Chiral amines play an important role in stereoselective organic synthesis. They are used directly as resolving agents, building blocks, or chiral auxiliaries.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service