ML 604086
CAS No. 850330-18-6
ML 604086( ML604086 )
Catalog No. M16173 CAS No. 850330-18-6
ML 604086 (ML604086) is a potent, selective CCR8 inhibitor that inhibits CCL1 mediated chemotaxis and increases in intracellular Ca2+ concentrations with IC50 of 1.3 uM and 1.0 uM respectively in cellular assays.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 97 | Get Quote |
|
| 5MG | 147 | Get Quote |
|
| 10MG | 259 | Get Quote |
|
| 25MG | 437 | Get Quote |
|
| 50MG | 624 | 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 NameML 604086
-
NoteResearch use only, not for human use.
-
Brief DescriptionML 604086 (ML604086) is a potent, selective CCR8 inhibitor that inhibits CCL1 mediated chemotaxis and increases in intracellular Ca2+ concentrations with IC50 of 1.3 uM and 1.0 uM respectively in cellular assays.
-
DescriptionML 604086 (ML604086) is a potent, selective CCR8 inhibitor that inhibits CCL1 mediated chemotaxis and increases in intracellular Ca2+ concentrations with IC50 of 1.3 uM and 1.0 uM respectively in cellular assays; displays high selectvity against a panel of 40 GPCRs, only moderately inhibits 5HT1a (30% at 10 uM).
-
In Vitro——
-
In VivoAnimal Model:3.0-5.0 kg male and female adult Macaca fascicularis (primate model of asthma)Dosage:1.038 mg/kg Administration:Intravenous infusion Result:Did not effected the Changes in airway resistance and compliance induced by allergen provocation and increasing concentrations of methacholine.
-
SynonymsML604086
-
PathwayGPCR/G Protein
-
TargetChemokine Receptor
-
RecptorChemokine Receptor
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number850330-18-6
-
Formula Weight508.637
-
Molecular FormulaC27H32N4O4S
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 120 mg/mL (235.93 mM)
-
SMILESO=C(NC1=C2C=CC=CC2=C(S(=O)(N[C@H]3[C@H](C)CN(C([C@@H](N)C)=O)CC3)=O)C=C1)C4=CC=CC=C4C
-
Chemical NameN-[4-[[[(3R,4R)-1-[(2S)-2-Amino-1-oxopropyl]-3-methyl-4-piperidinyl]amino]sulfonyl]-1-naphthalenyl]-2-methylbenzamide
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Jenkins TJ, et al. J Med Chem. 2007 Feb 8;50(3):566-84.
2. Wang L, et al. Thorax. 2013 Jun;68(6):506-12.
molnova catalog
related products
-
CXCR2-IN-68
CXCR2-IN-68 is a potent, selective, brain penetrant, and orally bioavailable CXCR2 antagonist with pIC50 of 9.0.
-
AZD 1678
AZD 1678 is a potent, selective orally bioavailable CCR4 receptor antagonist with pIC50 of 8.6 for hCCR4, pIC50 of 9.0 for rCCR4.
-
BX471
BX471 is a potent, selective, non-peptide CCR1 antagonist with Ki of 1 nM for hCCR1, displays 100 times less affinity for rat CCR1.
Cart
sales@molnova.com