D3658
1,9-Dideoxyforskolin from Coleus forskohlii
≥97%, solid
Synonym(s):
7β-Acetoxy-6β-hydroxy-8,13-epoxy-labd-14-en-11-one
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About This Item
Empirical Formula (Hill Notation):
C22H34O5
CAS Number:
Molecular Weight:
378.50
MDL number:
UNSPSC Code:
41106305
PubChem Substance ID:
NACRES:
NA.77
Quality Level
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 Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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