TEI-9648

SKU:BHB21900596
Research Validated
Overview
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TEI-9648 (CAS 173388-21-1) is an antagonist supplied as a solid. Relevant to Vitamin D Related/Nuclear Receptor research. Molecular formula C27H38O4, molecular weight 426.59 g/mol.
Purity 99.24%
CAS Number 173388-21-1
Molecular Weight 426.59 g/mol
Form Solid
Storage 4°C as supplied; in solvent -80°C
Options selector
Catalog no. Size
HY-12398A-1MG 1 mg
HY-12398A-5MG 5 mg
HY-12398A-10MG 10 mg
HY-12398A-50MG 50 mg
HY-12398A-100MG 100 mg
Available Options

Select the variant that best fits your experiment. Availability and lead time may vary by option.

  • Options: Size: 1 mg, 5 mg, 10 mg, 50 mg, 100 mg
  • Lead time: varies by selected option.
  • Storage: 4°C, protect from light, stored under nitrogen. In solvent: -80°C, 6 months; -20°C, 1 month (protect from light, stored under nitrogen).
  • Shipping: Room temperature in continental US; may vary elsewhere.
  • Upon receipt: refrigerate at 4°C as soon as possible.
Field Specification
CAS no. 173388-21-1
Applications
  • Functional Assay (In Vitro)
Molecular weight 426.59
Molecular formula C27H38O4
Purity 99.24%
SMILES O=C1O[C@H](C[C@H]([C@H]2CC[C@@]3([H])/C(CCC[C@]23C)=C/C=C4C([C@@H](O)C[C@H](O)C\4)=C)C)CC1=C
Form Solid
Storage 4°C, protect from light, stored under nitrogen. In solvent: -80°C, 6 months; -20°C, 1 month (protect from light, stored under nitrogen).
Shipping Room temperature in continental US; may vary elsewhere.
Catalog no. (Mfr.) HY-12398A
Main SKU BHB21900596
Antagonists

Compound Overview

TEI-9648, a vitamin D3 lactone analogue, is a potent and specific vitamin D receptor (VDR) antagonist. It inhibits VDR/VDRE-mediated genomic actions of 1α,25(OH)2D3 and also inhibits HL-60 cell differentiation induced by 1α,25(OH)2D3, and it has potential relevance to bone metabolism research[1][2]. It is supplied as an off-white to yellow solid (C27H38O4, MW 426.59) at 99.24% purity.

Physical & Chemical Properties

CAS Number 173388-21-1
Molecular Formula C27H38O4
Molecular Weight 426.59 g/mol
Purity 99.24%
Appearance Solid
Color Off-white to yellow
SMILES O=C1O[C@H](C[C@H]([C@H]2CC[C@@]3([H])/C(CCC[C@]23C)=C/C=C4C([C@@H](O)C[C@H](O)C\4)=C)C)CC1=C
Signaling Pathway Vitamin D Related/Nuclear Receptor
Solubility In Vitro: DMSO: 50 mg/mL (117.21 mM; Requires sonication and warming and heat to 60°C; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
Storage 4°C, protect from light, stored under nitrogen. In solvent: -80°C, 6 months; -20°C, 1 month (protect from light, stored under nitrogen).
Shipping Room temperature in continental US; may vary elsewhere.

Literature Cited

Sources cited in this description and in the In Vitro & In Vivo Data tab. Peer-reviewed publications that used this product are listed under References.

[1]. Miura D, et al. Antagonistic action of novel 1α,25-dihydroxyvitamin D3-26, 23-lactone analogs on differentiation of human leukemia cells (HL-60) induced by 1α,25-dihydroxyvitamin D3. J Biol Chem. 1999 Jun 4;274(23):16392-9.

[2]. Kazuya Takenouchi, et al. Synthesis and structure-activity relationships of TEI-9647 derivatives as Vitamin D3 antagonists. J Steroid Biochem Mol Biol. 2004 May;89-90(1-5):31-4.

Safety

For Research Use Only. Not for use in diagnostic or therapeutic procedures, and not for human or veterinary use. Handle in accordance with the Safety Data Sheet and your institution's chemical hygiene plan.

In Vitro

SolventSolubilityNotes
DMSO50 mg/mL (117.21 mM)requires sonication and warming and heat to 60°C; use freshly opened DMSO (absorbed moisture lowers solubility)

Aliquot the stock solution and store it at -80°C (up to 6 months) or -20°C (up to 1 month); protect from light, stored under nitrogen; avoid repeated freeze-thaw cycles.

Data provided by the manufacturer.

In Vitro

TEI-9648 (10-1000 nM) blocks, in a dose-dependent manner, the reciprocal changes of CD11b and CD71 expression that accompany HL-60 cell differentiation induced by 1α,25(OH)2D3[1]. TEI-9648 shows a consistently weaker suppressive effect than TEI-9647[1]. TEI-9648 cannot induce cell differentiation in HL-60 cells, even after treatment at 1 μM[1]. TEI-9648 alone cannot activate NBT-reducing activity or α-NB esterase activity. By contrast, in HL-60 cells, TEI-9648 markedly suppresses the up-regulation that 1α,25(OH)2D3 (0.1 nM) induces[1].

Data provided by the manufacturer. Numbered citations refer to the Literature Cited list in the product description.

Q.Why is there no price on some sizes?
A.Availability and lead time for those sizes are confirmed on inquiry. Send us the size you need and we will come back with price and lead time.
Q.Can this be used in humans or for diagnostics?
A.No. This product is supplied For Research Use Only. It is not for diagnostic or therapeutic procedures and not for human or veterinary use.

Need this compound in a format that drops straight into your assay? We can tailor formulation, chemistry, and documentation so your results stay consistent across runs and re-orders.

  • Format options: solid or pre-dissolved solution (choose solvent), target concentration, aliquots, light/moisture-protected packaging
  • Chemistry options: free base/acid vs salt forms, hydrate/solvate preference, stereoisomer control (single enantiomer or racemate), close analogs
  • Add-on labels & handles: D/¹³C/¹⁵N isotopes (LC-MS/internal standards), azide/alkyne or other functional handles for conjugation
  • QC & documentation: standard COA or enhanced analytical pack (HPLC/LC-MS/NMR), chiral purity, residual solvents, water content (KF), method-specific specs
  • Scale & continuity: mg to gram scale, bulk pricing, lot reservation, repeat-order continuity

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Antiviral activity of vitamin D derivatives against severe fever with thrombocytopenia syndrome virus in vitro and in vivo. Virol Sin 2024 Oct;39(5):802-811. PMID: 39168248

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