HomeProductsBuilding BlocksOrganic Building BlocksBenzene CompoundsOlvanil
Chemical structure of CAS 58493-49-5

Olvanil

In Stock•Starting at $36 for 1 mg•Purity ≥ 98%
CAS No.58493-49-5
MDL No.MFCD00673962
MFC26H43NO3
MW417.60
InChI KeyOPZKBPQVWDSATI-KHPPLWFESA-N

Pricing & Availability

Pack SizePurityPriceAvailabilityAction
1 mg98%$36In Stock
5 mg98%$96In Stock
10 mg98%$166In Stock
25 mg98%$329In Stock
50 mg98%$525In Stock
100 mg98%$837In Stock
Custom synthesis and bulk supply options are available upon request.

Product Information

N-Vanillyloleamide is a methoxybenzene and a phenol.

CAS No.58493-49-5
Product NameOlvanil
Heavy Atom Count30Rotatable Bond Count18
Atom Stereo Count0Bond Stereo Count1
HBA3HBD2
TPSA58.560 ŲCharge0
Exact Mass417.32429Complexity597.94
pKa8.400XLogP7.055

Related Articles

Studies related to this compound and its mechanism of action

Olvanil, a non-pungent vanilloid enhances the gastrointestinal toxicity of cisplatin in the ferret.

Toxicology letters • Vol. 192, Issue 3 • 2010
PMID: 19931602DOI: 10.1016/j.toxlet.2009.11.015

N-oleoyldopamine enhances glucose homeostasis through the activation of GPR119.

Molecular endocrinology (Baltimore, Md.) • Vol. 24, Issue 1 • 2010
PMID: 19901198PMC: PMC5428146DOI: 10.1210/me.2009-0239

TRPV1-mediated itch in seasonal allergic rhinitis.

Allergy • Vol. 64, Issue 5 • 2009
PMID: 19220220DOI: 10.1111/j.1398-9995.2009.01937.x

Signaling mechanisms of down-regulation of voltage-activated Ca2+ channels by transient receptor potential vanilloid type 1 stimulation with olvanil in primary sensory neurons.

Neuroscience • Vol. 141, Issue 1 • 2006
PMID: 16678970DOI: 10.1016/j.neuroscience.2006.03.023

Documentation

Similar Products