AMD 3465 hexahydrobromide - ≥97%, high purity , CAS No.185991-07-5

  • ≥97%
Item Number
A274943
Grouped product items
SKUSizeAvailabilityPrice Qty
A274943-2mg
2mg
In stock
$28.90
A274943-5mg
5mg
In stock
$59.90
A274943-10mg
10mg
In stock
$86.90
A274943-25mg
25mg
In stock
$195.90
A274943-50mg
50mg
In stock
$282.90
A274943-100mg
100mg
In stock
$521.90

Potent and selective CXCR4 antagonist

Basic Description

Specifications & Purity≥97%
Biochemical and Physiological MechanismsPotent and selective CXCR4 antagonist. Shows 8-fold greater affinity than AMD 3100 . Potent HIV entry inhibitor (IC 50 = ~10 nM). Additionally mobilizes stem cells in vivo .
Storage TempStore at -20°C,Desiccated
Shipped InIce chest + Ice pads
NoteWherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Product Description

Store at -20°C. Store under desiccating conditions. The product can be stored for up to 12 months.

Names and Identifiers

IUPAC Name N-(pyridin-2-ylmethyl)-1-[4-(1,4,8,11-tetrazacyclotetradec-1-ylmethyl)phenyl]methanamine;hexahydrobromide
INCHI InChI=1S/C24H38N6.6BrH/c1-2-13-29-24(5-1)20-28-19-22-6-8-23(9-7-22)21-30-17-4-12-26-15-14-25-10-3-11-27-16-18-30;;;;;;/h1-2,5-9,13,25-28H,3-4,10-12,14-21H2;6*1H
InChi Key ARHBIBDGWDRBJH-UHFFFAOYSA-N
Canonical SMILES C1CNCCNCCCN(CCNC1)CC2=CC=C(C=C2)CNCC3=CC=CC=N3.Br.Br.Br.Br.Br.Br
Isomeric SMILES C1CNCCNCCCN(CCNC1)CC2=CC=C(C=C2)CNCC3=CC=CC=N3.Br.Br.Br.Br.Br.Br
Alternate CAS 185991-24-6
PubChem CID 9897616
Molecular Weight 896.07

Certificates

Certificate of Analysis(COA)

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6 results found

Lot NumberCertificate TypeDateItem
B2307090Certificate of AnalysisNov 14, 2023 A274943
B2307085Certificate of AnalysisNov 14, 2023 A274943
B2307084Certificate of AnalysisNov 14, 2023 A274943
B2307097Certificate of AnalysisNov 14, 2023 A274943
B2307081Certificate of AnalysisNov 14, 2023 A274943
B2307020Certificate of AnalysisNov 14, 2023 A274943

Chemical and Physical Properties

SolubilitySoluble in water to 50 mM and in DMSO to 25 mM
SensitivityMoisture sensitive

Safety and Hazards(GHS)

RIDADR NONHforallmodesoftransport

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References

1. Hatse S et al..  (2005)  AMD3465, a monomacrocyclic CXCR4 antagonist and potent HIV entry inhibitor..  Biochem Pharmacol,  70  (5): (752-61).  [PMID:16011832]
2. Hu JS et al..  (2006)  AMD3465, a novel CXCR4 receptor antagonist, abrogates schistosomal antigen-elicited (type-2) pulmonary granuloma formation..  Am J Pathol,  169  (2): (424-32).  [PMID:16877345]
3. Bodart V et al..  (2009)  Pharmacology of AMD3465: a small molecule antagonist of the chemokine receptor CXCR4..  Biochem Pharmacol,  78  (8): (993-1000).  [PMID:19540208]
4. Forte D et al..  (2017)  The tissue inhibitor of metalloproteinases-1 (TIMP-1) promotes survival and migration of acute myeloid leukemia cells through CD63/PI3K/Akt/p21 signaling..  Oncotarget,  (2): (2261-2274).  [PMID:27903985]

Solution Calculators