CAS 153559-49-0|Bexarotene

Introduction:Basic information about CAS 153559-49-0|Bexarotene, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common NameBexarotene
CAS Number153559-49-0Molecular Weight348.478
Density1.0±0.1 g/cm3Boiling Point489.7±44.0 °C at 760 mmHg
Molecular FormulaC24H28O2Melting Point230-231ºC
MSDSChineseUSAFlash Point229.5±23.1 °C

Names

Namebexarotene
SynonymMore Synonyms

Bexarotene BiologicalActivity

DescriptionBexarotene is a selective retinoid X receptors (RXR) agonist for the treatment of cutaneous T-cell lymphoma.
Related CatalogSignaling Pathways >>Autophagy >>AutophagySignaling Pathways >>Metabolic Enzyme/Protease >>RAR/RXRResearch Areas >>Cancer
References

[1]. Vakeva L, Ranki A, Hahtola S.Ten-year experience of bexarotene therapy for cutaneous T-cell lymphoma in Finland.Acta Derm Venereol. 2012 May;92(3):258-63. doi: 10.2340/00015555-1359.

[2]. Zhang X, Schlaak M, Fabri M, Mauch C, Kurschat P.Successful Treatment of a Panniculitis-Like Primary Cutaneous T-Cell Lymphoma of the α/β Type with Bexarotene.Case Rep Dermatol. 2012 Jan;4(1):56-60.

[3]. Orendas P, Kubatka P, Kajo K, Stollarova N, Kassayova M, Bojkova B, Pec M, Nosal V, Kiskova T, Zihlavnikova K, Karsnakova R.Melatonin enhanced bexarotene efficacy in experimental mammary carcinogenesis.Neoplasma. 2012;59(4):469-74.

[4]. Cras A, Politis B, Balitrand N, Darsin-Bettinger D, Boelle PY, Cassinat B, Toubert ME, Chomienne C.Bexarotene via CBP/p300 induces suppression of NF-κB-dependent cell growth and invasion in thyroid cancer.Clin Cancer Res. 2012 Jan 15;18(2):442-53.

[5]. Gui Y, et al. Bexarotent attenuated CCI-induced spinal neuroinflammation and neuropathic pain by targeting MKP-1. J Pain. 2019 Jan 17. pii: S1526-5900(18)30607-2.

Chemical & Physical Properties

Density1.0±0.1 g/cm3
Boiling Point489.7±44.0 °C at 760 mmHg
Melting Point230-231ºC
Molecular FormulaC24H28O2
Molecular Weight348.478
Flash Point229.5±23.1 °C
Exact Mass348.208923
PSA37.30000
LogP8.55
Vapour Pressure0.0±1.3 mmHg at 25°C
Index of Refraction1.556
InChIKeyNAVMQTYZDKMPEU-UHFFFAOYSA-N
SMILESC=C(c1ccc(C(=O)O)cc1)c1cc2c(cc1C)C(C)(C)CCC2(C)C

Safety Information

Hazard CodesXn
RIDADRNONH for all modes of transport

Articles18

More Articles
Retinoids Bias Integrin Expression and Function in Cutaneous T-Cell Lymphoma.

J. Invest. Dermatol. 135 , 2102-8, (2015)

Cutaneous T-cell lymphoma (CTCL) is a heterogeneous group of malignancies characterized by accumulation of malignant T-cells within the skin. Retinoids, metabolic derivatives, and synthetic analogs of...

RNA-sequencing reveals transcriptional up-regulation of Trem2 in response to bexarotene treatment.

Neurobiol. Dis. 82 , 132-40, (2015)

We have recently demonstrated that short term bexarotene treatment of APP/PS1 mice significantly improves their cognitive performance. While there were no changes in plaque load, or insoluble Aβ level...

Retinoid X receptors orchestrate osteoclast differentiation and postnatal bone remodeling.

J. Clin. Invest. 125(2) , 809-23, (2015)

Osteoclasts are bone-resorbing cells that are important for maintenance of bone remodeling and mineral homeostasis. Regulation of osteoclast differentiation and activity is important for the pathogene...

Synonyms

Targretin
Bexarotene
4-[1-(3,5,5,8,8-Pentamethyl-5,6,7,8-tetrahydronaphthalen-2-yl)vinyl]benzoic acid
LG 69
4-[1-(3,5,5,8,8-Pentamethyl-5,6,7,8-tetrahydro-2-naphthalenyl)vinyl]benzoic acid
Lg 1069
4-[1-(3,5,5,8,8-Pentamethyl-5,6,7,8-tetrahydro-naphthalen-2-yl)-vinyl]-benzoic acid
Targretyn
Bexaroten
Targret
Benzoic acid, 4-[1-(5,6,7,8-tetrahydro-3,5,5,8,8-pentamethyl-2-naphthalenyl)ethenyl]-
4-[1-(3,5,5,8,8-Pentamethyl-2-5,8-dihydronaphthyl)vinyl]benzoic acid
4-[1-(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydronaphthalen-2-yl)ethenyl]benzoic acid
LGD1069
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