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Dexamethasone sodium succinate

CAT: 0931-T69323-01Size: 100 mgDry Ice: NoHazardous: No
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CAT#:0931-T69323-01Size:100 mg
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CAS Number
3800-84-8
Target
Others
Related Pathways
Others
Bioactivity
Dexamethasone sodium succinate is the acetate salt form of dexamethasone, which is a synthetic glucocorticoid; it combines high anti-inflammatory effects with low mineralocorticoid activity. At high doses (e.g. 40 mg), it reduces the immune response. Dexamethasone acetate (NEOFORDEX®) is indicated in adults for the treatment of symptomatic multiple myeloma in combination with other medicinal products. Dexamethasone has been shown to induce multiple myeloma cell death (apoptosis) via a down-regulation of nuclear factor-κB activity and an activation of caspase-9 through second mitochondria-derived activator of caspase (Smac; an apoptosis promoting factor) release. Prolonged exposure was required to achieve maximum levels of apoptotic markers along with increased caspase-3 activation and DNA fragmentation. Dexamethasone also down-regulated anti apoptotic genes and increased IκB-alpha protein levels. Dexamethasone apoptotic activity is enhanced by the combination with thalidomide......
Smiles
C[C@@]12[C@](C[C@H]([C@]2(O)C(COC(CCC([O-])=O)=O)=O)C)([H])[C@@]3([H])[C@]([C@H](C1)O)([C@@]4(C(CC3)=CC(C=C4)=O)C)F.[Na+]
Molecular Formula
C26H32FNaO8
Molecular Weight
514.52
Shipping Conditions
Ice Packs
Storage Temperature
-20°C

Chemical Information

Dexamethasone sodium succinate

Dexamethasone Sodium Succinate is the sodium succinate salt form of dexamethasone, a synthetic adrenal corticosteroid and derivative of hydrocortisone, with potent anti-inflammatory properties. In addition to binding to specific nuclear steroid receptors, dexamethasone also interferes with NF-kB activation and apoptotic pathways. This agent lacks the salt-retaining properties of other related adrenal hormones.

CAS Number3800-84-8
PubChem CID90479300
IUPAC Namesodium 4-[2-[(8S,9R,10S,11S,13S,14S,16R,17R)-9-fluoro-11,17-dihydroxy-10,13,16-trimethyl-3-oxo-6,7,8,11,12,14,15,16-octahydrocyclopenta[a]phenanthren-17-yl]-2-oxoethoxy]-4-oxobutanoate
Molecular FormulaC26H32FNaO8
Molecular Weight514.5
Topological Polar Surface Area141
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count9
Rotatable Bond Count7
Heavy Atom Count36
Formal Charge0
Complexity1040
SMILES
C[C@@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@@]4([C@]3([C@H](C[C@@]2([C@]1(C(=O)COC(=O)CCC(=O)[O-])O)C)O)F)C.[Na+]
InChI
InChI=1S/C26H33FO8.Na/c1-14-10-18-17-5-4-15-11-16(28)8-9-23(15,2)25(17,27)19(29)12-24(18,3)26(14,34)20(30)13-35-22(33)7-6-21(31)32;/h8-9,11,14,17-19,29,34H,4-7,10,12-13H2,1-3H3,(H,31,32);/q;+1/p-1/t14-,17+,18+,19+,23+,24+,25+,26+;/m1./s1
InChIKey
VEMKNVZPCCPUIL-NJVDTJLMSA-M
Chemical Structure
2D Structure
2D structure of Dexamethasone sodium succinate
CAS: 3800-84-8
CID: 90479300
Formula: C26H32FNaO8
MW: 514.5
Interactive 3D Structure
Loading 3D structure...
Computed Properties
PropertyValue
Molecular Weight514.5
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count9
Rotatable Bond Count7
Exact Mass514.19789042
Monoisotopic Mass514.19789042
Topological Polar Surface Area141 Ų
Heavy Atom Count36
Formal Charge0
Complexity1040
Isotope Atom Count0
Defined Atom Stereocenter Count8
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently-Bonded Unit Count2
Compound Is CanonicalizedYes