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Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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SKU | Size | Availability | Price | Qty |
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M125486-5mg | 5mg | In stock | $58.90 | |
M125486-25mg | 25mg | In stock | $265.90 | |
M125486-100mg | 100mg | Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience! | $616.90 |
Potent and selective CCR5 antagonist with potent anti-HIV activity
Synonyms | UK-427857 |
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Specifications & Purity | Moligand™, ≥98% |
Biochemical and Physiological Mechanisms | Maraviroc (UK-427857; Selzentry; Celsentri) is a Selective CCR5 antagonist; displays potent anti-HIV-1 activity. Maraviroc (UK-427857; Selzentry; Celsentri) prevents the interaction of HIV-1 gp120 and CCR5 (IC50 = 6.4 nM), inhibiting HIV-1 entry. Maraviro |
Legal Information | Sold for only research purposes |
Storage Temp | Store at -20°C |
Shipped In | Ice chest + Ice pads |
Grade | Moligand™ |
Action Type | ANTAGONIST |
Mechanism of action | C-C chemokine receptor type 5 antagonist |
Note | Toxic, refer to SDS for further information. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details. |
Product Description | Maraviroc has been used as a C-C chemokine receptor type 5 (CCR5-specific) inhibitor in murine monocyte/macrophage cell line J774A.1, porcine uterine luminal epithelial cells and human lung CD4+ T cells. |
ALogP | 5.1 |
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Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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IUPAC Name | 4,4-difluoro-N-[(1S)-3-[(1S,5R)-3-(3-methyl-5-propan-2-yl-1,2,4-triazol-4-yl)-8-azabicyclo[3.2.1]octan-8-yl]-1-phenylpropyl]cyclohexane-1-carboxamide |
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INCHI | InChI=1S/C29H41F2N5O/c1-19(2)27-34-33-20(3)36(27)25-17-23-9-10-24(18-25)35(23)16-13-26(21-7-5-4-6-8-21)32-28(37)22-11-14-29(30,31)15-12-22/h4-8,19,22-26H,9-18H2,1-3H3,(H,32,37)/t23-,24+,25?,26-/m0/s1 |
InChi Key | GSNHKUDZZFZSJB-HLMSNRGBSA-N |
Canonical SMILES | CC1=NN=C(N1C2CC3CCC(C2)N3CCC(C4=CC=CC=C4)NC(=O)C5CCC(CC5)(F)F)C(C)C |
Isomeric SMILES | CC1=NN=C(N1C2C[C@H]3CC[C@@H](C2)N3CC[C@@H](C4=CC=CC=C4)NC(=O)C5CCC(CC5)(F)F)C(C)C |
WGK Germany | 1 |
Alternate CAS | 2414315-81-2,376348-65-1 |
PubChem CID | 3002977 |
MeSH Entry Terms | 4,4-difluoro-N-((1S)-3-(exo-3-(3-isopropyl-5-methyl-4H-1,2,4-triazol-4-yl)-8-azabicyclo(3.2.1)oct-8-yl)-1-phenylpropyl)cyclohexanecarboxamide;maraviroc;Selzentry;UK 427,857;UK 427857;UK-427,857;UK-427857;UK427,857;UK427857 |
Molecular Weight | 513.67 |
PubChem CID | 3002977 |
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Wikipedia | Maraviroc |
DrugBank Ligand | DB04835 |
CAS Registry No. | 376348-65-1 |
GPCRdb Ligand | maraviroc |
Enter Lot Number to search for COA:
Find and download the COA for your product by matching the lot number on the packaging.
Lot Number | Certificate Type | Date | Item |
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K2301452 | Certificate of Analysis | Oct 25, 2023 | M125486 |
K2301453 | Certificate of Analysis | Oct 25, 2023 | M125486 |
K2301454 | Certificate of Analysis | Oct 25, 2023 | M125486 |
J2127239 | Certificate of Analysis | Aug 01, 2023 | M125486 |
I2219220 | Certificate of Analysis | Jul 21, 2022 | M125486 |
I2219221 | Certificate of Analysis | Jul 21, 2022 | M125486 |
I2219222 | Certificate of Analysis | Jul 21, 2022 | M125486 |
Solubility | DMSO: >30 mg/ml |
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Pictogram(s) | GHS08 |
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Signal | Warning |
Hazard Statements | H373:Causes damage to organs through prolonged or repeated exposure H412:Harmful to aquatic life with long lasting effects |
Precautionary Statements | P273:Avoid release to the environment. P501:Dispose of contents/container to ... P260:Do not breathe dust/fume/gas/mist/vapors/spray. P319:Get medical help if you feel unwell. |
WGK Germany | 1 |
1. Dorr P, Westby M, Dobbs S, Griffin P, Irvine B, Macartney M, Mori J, Rickett G, Smith-Burchnell C, Napier C et al.. (2005) Maraviroc (UK-427,857), a potent, orally bioavailable, and selective small-molecule inhibitor of chemokine receptor CCR5 with broad-spectrum anti-human immunodeficiency virus type 1 activity.. Antimicrob Agents Chemother, 49 (11): (4721-32). [PMID:16251317] [10.1021/op500134e] |
2. Mencarelli A, Cipriani S, Francisci D, Santucci L, Baldelli F, Distrutti E, Fiorucci S. (2016) Highly specific blockade of CCR5 inhibits leukocyte trafficking and reduces mucosal inflammation in murine colitis.. Sci Rep, 6 (13): (30802). [PMID:27492684] [10.1021/op500134e] |
3. Takeuchi T, Kameda H. (2012) What is the future of CCR5 antagonists in rheumatoid arthritis?. Arthritis Res Ther, 14 (2): (114). [PMID:22494450] [10.1021/op500134e] |
4. Christopoulos A, Changeux JP, Catterall WA, Fabbro D, Burris TP, Cidlowski JA, Olsen RW, Peters JA, Neubig RR, Pin JP et al.. (2014) International union of basic and clinical pharmacology. XC. multisite pharmacology: recommendations for the nomenclature of receptor allosterism and allosteric ligands.. Pharmacol Rev, 66 (4): (918-47). [PMID:25026896] [10.1021/op500134e] |