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Home CSCS03549788088

Methyl (1S,2R,18R,19R,22R,34S,37R,40R,52S)-22-amino-2-{[(2S,4R,5R,6S)-4-amino-5-hydroxy-6-methyloxan-2-yl]oxy}-64-{[(2S,3R,4S,5S,6R)-3-{[(2S,3R,4R,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-{[(2S,3S,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxy}oxan-2-yl]oxy}-4,5-dihydroxy-6-({[(3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}methyl)oxan-2-yl]oxy}-18,26,31,44,49-pentahydroxy-30-methyl-21,35,38,54,56,59-hexaoxo-47-{[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-7,13,28-trioxa-20,36,39,53,55,58-hexaazaundecacyclo[38.14.2.2³,⁶.2¹⁴,¹⁷.2¹⁹,³⁴.1⁸,¹².1²³,²⁷.1²⁹,³³.1⁴¹,⁴⁵.0¹⁰,³⁷.0⁴⁶,⁵¹]hexahexaconta-3,5,8(64),9,11,14,16,23,25,27(61),29(60),30,32,41,43,45(57),46,48,50,62,65-henicosaene-52-carboxylate


Structure Info


Chemspace ID
CSCS03549788088 (Synthesis)
IUPAC Name
methyl (1S,2R,18R,19R,22R,34S,37R,40R,52S)-22-amino-2-{[(2S,4R,5R,6S)-4-amino-5-hydroxy-6-methyloxan-2-yl]oxy}-64-{[(2S,3R,4S,5S,6R)-3-{[(2S,3R,4R,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-{[(2S,3S,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxy}oxan-2-yl]oxy}-4,5-dihydroxy-6-({[(3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}methyl)oxan-2-yl]oxy}-18,26,31,44,49-pentahydroxy-30-methyl-21,35,38,54,56,59-hexaoxo-47-{[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-7,13,28-trioxa-20,36,39,53,55,58-hexaazaundecacyclo[38.14.2.2³,⁶.2¹⁴,¹⁷.2¹⁹,³⁴.1⁸,¹².1²³,²⁷.1²⁹,³³.1⁴¹,⁴⁵.0¹⁰,³⁷.0⁴⁶,⁵¹]hexahexaconta-3,5,8(64),9,11,14,16,23,25,27(61),29(60),30,32,41,43,45(57),46,48,50,62,65-henicosaene-52-carboxylate
Mol formula
C95H110N8O44
Mol weight
2068 Da
Catalog Number(s)
AKOS040747397, FR29315, T26093

Properties

LogP
-7.77
Heavy atoms count
147
Rotatable bond count
17
Number of rings
17
Carbon bond saturation, Fsp3
0.48421052631579
Polar surface area (Å)
816
Hydrogen bond acceptors count
42
Hydrogen bond donors count
29

SDS

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Items Overall 1 item from 1 supplier

SupplierLead timeShips fromPurityPackPrice, $Qty
Targetmol Chemicals IncTBDUnited States
To:
901 mgPOA
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Description: Ristocetin is a glycopeptide antibiotic that functions as a potent activator of von Willebrand factor, specifically by promoting its interaction with platelet glycoprotein Ib/IX/V to trigger platelet aggregation. The compound synergistically induces platelet activation when combined with CXCL12 at subthreshold doses, a process mediated through Rac signaling and negatively regulated by the Rho/Rho-kinase pathway. In research applications, ristocetin is widely used as a tool to investigate platelet function, integrin signaling, and the molecular mechanisms underlying hemostasis and thrombosis.; CAS: 1404-55-3
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