Home - Products - Endocrinology/Hormones - Opioid Receptor - Propiram fumarate HCl

Propiram fumarate HCl

CAS No. 945013-73-0

Propiram fumarate HCl( —— )

Catalog No. M34385 CAS No. 945013-73-0

Propiram fumarate HClis an orally available Opioid receptors agonist with analgesic activity for the study of musculoskeletal pain.

Purity : >98% (HPLC)

COA

Datasheet

HNMR

HPLC

MSDS

Handing Instructions

Size	Price / USD	Stock	Quantity
2MG	296	Get Quote
5MG	409	Get Quote
10MG	604	Get Quote
25MG	908	Get Quote
50MG	1251	Get Quote
100MG	1647	Get Quote
200MG	Get Quote	Get Quote
500MG	3312	Get Quote
1G	Get Quote	Get Quote

Get Quotation Bulk Inquiry Add to Cart

Biological Information

Product Name

Propiram fumarate HCl
Note

Research use only, not for human use.
Brief Description

Propiram fumarate HClis an orally available Opioid receptors agonist with analgesic activity for the study of musculoskeletal pain.
Description

Propiram fumarate HClis an orally available Opioid receptors agonist with analgesic activity for the study of musculoskeletal pain.
In Vitro

——
In Vivo

——
Synonyms

——
Pathway

Endocrinology/Hormones
Target

Opioid Receptor
Recptor

Opioid Receptor
Research Area

——
Indication

——

Chemical Information

CAS Number

945013-73-0
Formula Weight
Molecular Formula

C16H25N3O.xClH
Purity

>98% (HPLC)
Solubility

——
SMILES

Cl.CCC(=O)N(C(C)CN1CCCCC1)c1ccccn1
Chemical Name

——

Shipping & Storage Information

Storage

(-20℃)
Shipping

With Ice Pack
Stability

≥ 2 years

Reference

Calculator

Molecular Weight Calculator

Dilution Calculator

Molarity Calculator

molnova catalog

related products

(20R)-Protopanaxdiol

Protopanaxdiol has the effect of anti-tumor through increasing the activity of body immunity, inhibiting tumor interstitial microvascular density and its proliferation activity.
Deltorphin

Deltorphin (Dermenkephalin) is Isolated from the skin of Phyllomedusa Sauvage. It also has an affinity to the opioid receptor.
Ac-RYYRIK-NH2

High affinity ligand for the NOP site (Ki = 1.5 nM). Antagonizes nociceptin-stimulated GTP binding in rat brain and the chronotropic effect of nociceptin on rat cardiomyocytes. However, displays potent agonist properties in vivo, inhibiting locomotor activity in mice.

Sign In Join Free