Cart
sales@molnova.com
Olvanil
CAS No. 58493-49-5
Olvanil ( N-Vanillyloleamide; N-Vannilyloleoylamide )
Catalog No. M27675 CAS No. 58493-49-5
Olvanil is a vanilloid receptor agonist with EC50 of 0.7nM.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 102 | Get Quote |
|
| 5MG | 170 | Get Quote |
|
| 10MG | 250 | Get Quote |
|
| 25MG | 428 | Get Quote |
|
| 50MG | 614 | Get Quote |
|
| 100MG | 853 | Get Quote |
|
| 500MG | 1692 | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameOlvanil
-
NoteResearch use only, not for human use.
-
Brief DescriptionOlvanil is a vanilloid receptor agonist with EC50 of 0.7nM.
-
DescriptionOlvanil is a vanilloid receptor agonist with EC50 of 0.7nM.(In Vitro):Olvanil affects C6 glioma cell proliferation with IC50 of 5.5 μM.(In Vivo):Olvanil is one capsaicin analog. Olvanil acts as an agonist at the vanilloid receptor. Olvanil may have causes an anxiogenic-like effect. Doses of 0, 0.2, 1.0 and 5.0 mg/kg Olvanil, respectively, yielded percent open arm entries at 5 min of 25±10.1, 19.3±7.1, 14.9±5.9 and 0±0.
-
SynonymsN-Vanillyloleamide; N-Vannilyloleoylamide
-
PathwayMembrane Transporter/Ion Channel
-
TargetTRP/TRPV Channel
-
RecptorHDAC
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number58493-49-5
-
Formula Weight417.6
-
Molecular FormulaC26H43NO3
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESCCCCCCCC\C=C/CCCCCCCC(=O)NCc1ccc(O)c(OC)c1
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Han-Li Huang, et al. TIMP3 expression associates with prognosis in colorectal cancer and its novel arylsulfonamide inducer, MPT0B390, inhibits tumor growth, metastasis and angiogenesis. Theranostics. 2019 Sep 18;9(22):6676-6689.
molnova catalog
related products
-
AMG-517
AMG 517 is a potent and selective TRPV1 antagonist, antagonizes capsaicin, proton, and heat activation of TRPV1 with IC50 of 0.76 nM, 0.62 nM and 1.3 nM.
-
Asivatrep
Asivatrep (PAC-14028) is a potent, selective TRPV1 antagonist with IC50 of 55 nM against capsaicin-induced Ca2+ influx in rat DRG neurons.
-
EIPA
EIPA (L593754, MH 12-43) is a TRPP3 channel inhibitor (IC50: 10.5 μM). It also inhibits Na+/H+-exchanger (NHE) and macropinocytosis.It is found that EIPA, benzamil, and phenamil rapidly and reversibly block Ca2+-activated TRPP3 channel activation at -50 mV, with IC50s of 143, 10.5, 1.1, and 0.14 μM, respectively.
