PeptideDB

CD 3159 180713-37-5

CD 3159 180713-37-5

CAS No.: 180713-37-5

LG-100754 (CD-3159; UVI-2112) is a novel and potent retinoic acid receptors antagonistagonistor RXR dimers modulater. Sp
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This product is for research use only, not for human use. We do not sell to patients.

LG-100754 (CD-3159; UVI-2112) is a novel and potent retinoic acid receptors antagonist & agonist or RXR dimers modulater. Specifically, it acts as a RXR:RXR homodimer antagonist, but functions as a agonist towards RXR:PPARα and RXR:PPARγ heterodimers. LG100754 is an insulin sensitizer that functions through RXR.



Physicochemical Properties


Molecular Formula C26H36O3
Molecular Weight 396.57
Exact Mass 396.266
CAS # 180713-37-5
PubChem CID 6442223
Appearance White to off-white solid powder
Density 1.003g/cm3
Boiling Point 549.4ºC at 760 mmHg
Flash Point 178.5ºC
Vapour Pressure 6.63E-13mmHg at 25°C
Index of Refraction 1.526
LogP 6.814
Hydrogen Bond Donor Count 1
Hydrogen Bond Acceptor Count 3
Rotatable Bond Count 7
Heavy Atom Count 29
Complexity 665
Defined Atom Stereocenter Count 0
SMILES

CCCOC1=CC2=C(C=C1/C(=C\C=C\C(=C\C(=O)O)\C)/C)C(CCC2(C)C)(C)C

InChi Key HNODNXQAYXJFMQ-LQUSFLDPSA-N
InChi Code

InChI=1S/C26H36O3/c1-8-14-29-23-17-22-21(25(4,5)12-13-26(22,6)7)16-20(23)19(3)11-9-10-18(2)15-24(27)28/h9-11,15-17H,8,12-14H2,1-7H3,(H,27,28)/b10-9+,18-15+,19-11-
Chemical Name

(2E,4E,6Z)-3-methyl-7-(5,5,8,8-tetramethyl-3-propoxy-6,7-dihydronaphthalen-2-yl)octa-2,4,6-trienoic acid
Synonyms

LG100754 UVI2112 CD3159 LG-100754 CD-3159 UVI-2112 CD-3159 CD 3159
HS Tariff Code 2934.99.9001
Storage

Powder-20°C 3 years

4°C 2 years

In solvent -80°C 6 months

-20°C 1 month

Shipping Condition Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs)

Biological Activity


ln Vitro One specific activator of endogenous RXR heterodimers is LG100754 [1]. In mature adipocytes, TNFα-mediated insulin resistance can also be ameliorated by LG100754 [1]. Genuine activation of the endogenous RXR:PPARγ heterodimer and modulation of insulin-dependent signaling pathways are exhibited by LG100754 [1].
ln Vivo The fact that LG100754 (100 mg/kg) totally prevents the rise in glucose levels suggests that LG100754 can help the body become more insulin resistant [1].
References

[1]. The rexinoid LG100754 is a novel RXR:PPARgamma agonist and decreases glucose levels in vivo. Mol Endocrinol. 2001 Aug;15(8):1360-9.


Solubility Data


Solubility (In Vitro) DMSO : ~100 mg/mL (~252.17 mM)
Solubility (In Vivo) Solubility in Formulation 1: 2.5 mg/mL (6.30 mM) in 10% DMSO + 90% Corn Oil (add these co-solvents sequentially from left to right, and one by one), clear solution; with sonication.
For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 25.0 mg/mL clear DMSO stock solution to 900 μL of corn oil and mix evenly.

 (Please use freshly prepared in vivo formulations for optimal results.)
Preparing Stock Solutions 1 mg 5 mg 10 mg
1 mM 2.5216 mL 12.6081 mL 25.2162 mL
5 mM 0.5043 mL 2.5216 mL 5.0432 mL
10 mM 0.2522 mL 1.2608 mL 2.5216 mL
*Note: Please select an appropriate solvent for the preparation of stock solution based on your experiment needs. For most products, DMSO can be used for preparing stock solutions (e.g. 5 mM, 10 mM, or 20 mM concentration); some products with high aqueous solubility may be dissolved in water directly. Solubility information is available at the above Solubility Data section. Once the stock solution is prepared, aliquot it to routine usage volumes and store at -20°C or -80°C. Avoid repeated freeze and thaw cycles.