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About This Item
Empirical Formula (Hill Notation):
C22H34O5
CAS Number:
Molecular Weight:
378.50
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
41106305
MDL number:
Assay:
≥97%
Form:
solid
Quality Segment
assay
≥97%
form
solid
optical activity
[α]26/D +93.6°, c = 6.12 in chloroform(lit.)
color
white to off-white
solubility
methanol: 28 mg/mL(lit.), DMSO: 3 mg/mL(lit.), chloroform: 50 mg/mL, ethanol: 6.6 mg/mL(lit.), dilute aqueous acid and base: insoluble(lit.)
storage temp.
−20°C
SMILES string
[H][C@@]12[C@H](O)[C@H](OC(C)=O)[C@@]3(C)O[C@](C)(CC(=O)C3[C@@]1(C)CCCC2(C)C)C=C
InChI
1S/C22H34O5/c1-8-20(5)12-14(24)16-21(6)11-9-10-19(3,4)17(21)15(25)18(26-13(2)23)22(16,7)27-20/h8,15-18,25H,1,9-12H2,2-7H3/t15-,16?,17-,18-,20-,21+,22-/m0/s1
InChI key
ZKZMDXUDDJYAIB-OJPJTMFRSA-N
Application
Useful as a negative control for forskolin.
Biochem/physiol Actions
Biologically inactive forskolin analog. Does not stimulate adenylyl cyclase.
Features and Benefits
This compound is a featured product for Cyclic Nucleotide research. Click here to discover more featured Cyclic Nucleotide products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.
This compound is featured on the Adenylyl cyclases page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Global Trade Item Number
| SKU | GTIN |
|---|---|
| D3658-1MG | 04061826674444 |
| D3658-5MG | 04061832897806 |