Home -
Products -
Others -
Other Targets -
H-Phe(4-Cl)-D-Cys-β-(3-pyridyl)-Ala-D-Trp-N-Me-Lys-Thr-Cys-2-Nal-NH2
H-Phe(4-Cl)-D-Cys-β-(3-pyridyl)-Ala-D-Trp-N-Me-Lys-Thr-Cys-2-Nal-NH2
CAS No. 341519-04-8
H-Phe(4-Cl)-D-Cys-β-(3-pyridyl)-Ala-D-Trp-N-Me-Lys-Thr-Cys-2-Nal-NH2( ——— )
Catalog No. M40407 CAS No. 341519-04-8
PRL 3195 is a somatostatin receptor antagonist with Kis of 6, 17, 66, 1000 and 1000 nM for human somatostatin receptors (sst5, sst2, sst3, sst1 and sst4, respectively).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 25MG | Get Quote | Get Quote |
|
| 50MG | Get Quote | Get Quote |
|
| 100MG | Get Quote | Get Quote |
|
| 200MG | Get Quote | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameH-Phe(4-Cl)-D-Cys-β-(3-pyridyl)-Ala-D-Trp-N-Me-Lys-Thr-Cys-2-Nal-NH2
-
NoteResearch use only, not for human use.
-
Brief DescriptionPRL 3195 is a somatostatin receptor antagonist with Kis of 6, 17, 66, 1000 and 1000 nM for human somatostatin receptors (sst5, sst2, sst3, sst1 and sst4, respectively).
-
DescriptionPRL 3195 is a somatostatin receptor antagonist with Kis of 6, 17, 66, 1000 and 1000 nM for human somatostatin receptors (sst5, sst2, sst3, sst1 and sst4, respectively).
-
In Vitro———
-
In Vivo———
-
Synonyms———
-
PathwayOthers
-
TargetOther Targets
-
Recptorhsst5: 6 nM (Ki), hsst2: 17 nM (Ki), hsst3: 66 nM (Ki), hsst1: 1000 nM (Ki), hsst4: 1000 nM (Ki), rat urotensin II receptor: 429 nM (Ki), human urotensin II receptor: 1846 nM (Ki)]
-
Research Area———
-
Indication———
Chemical Information
-
CAS Number341519-04-8
-
Formula Weight1177.83
-
Molecular FormulaC58H69ClN12O9S2
-
Purity>98% (HPLC)
-
Solubility———
-
SMILES———
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Rossowski WJ, et al. Human urotensin II-induced aorta ring contractions are mediated by protein kinase C, tyrosine kinases and Rho-kinase: inhibition by somatostatin receptor antagonists. Eur J Pharmacol. 2002 Mar 8;438(3):159-70.?
molnova catalog
related products
-
Uridine
Uridine, Trisodium Salt is an energy-rich precursor in the enzymatic biosynthesis of RNA, a potent vasodilator, and induces contractile responses in some tissues.
-
Sulbactum Sodium
Sulbactum Sodium is synthesized from cytidine monophosphate (CMP) or uridine monophosphate (UMP) by the transfer of phosphoryl group, catalyzed by the enzyme uridylate kinase (UMPK).
-
Leucoside
Leucoside is a naturally occuring flavonol bioside with many biological activities.
Cart
sales@molnova.com