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Home CSCS06595020978

Structure Info

Chemspace ID
CSCS06595020978 (Synthesis)
IUPAC Name
(1S,3S,4S,5R,6R,7R)-1-[(4R,5R)-4-(acetyloxy)-5-methyl-6-phenylhexyl]-4,7-dihydroxy-6-{[(4E,6R)-6-methyl-9-phenylnon-4-enoyl]oxy}-2,8-dioxabicyclo[3.2.1]octane-3,4,5-tricarboxylic acid
Mol formula
C40H50O14
Mol weight
755 Da
Catalog Number(s)
HY-125400, T24710

Properties

LogP
6.3
Heavy atoms count
54
Rotatable bond count
22
Number of rings
4
Carbon bond saturation, Fsp3
0.525
Polar surface area (Å)
223
Hydrogen bond acceptors count
12
Hydrogen bond donors count
5

SDS

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C40H50O14
Zoom the structure
CSCS06595020978
 

Items Overall 5 items from 3 suppliers

SupplierLead timeShips fromPurityPackPrice, $Qty
Targetmol Chemicals Inc30 daysUnited States
To:
9025 mg6,770
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Targetmol Chemicals Inc30 daysUnited States
To:
9050 mg8,980
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Targetmol Chemicals Inc30 daysUnited States
To:
90100 mg13,000
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Description: Zaragozic acid C is an effective inhibitor of squalene synthase.; CAS: 146389-62-0
MedChemExpressTBDUnited States
To:
901 mgPOA
Go to cartEnquire
Description: Names: Zaragozic acid C; L-697350; Product Description: Zaragozic acid C (L-697350) is a potent sterol synthase inhibitor with potential antitumor activity. Zaragozic acid C contains multiple hydroxyl and alkyl substituents in its chemical structure, demonstrating complex functionalization capabilities. The synthesis of zaragozic acid C involves a photochemical C(sp3)-H acylation reaction, which resolves the challenging carbon substitution problem in the synthesis .; Target: Endogenous Metabolite; CAS: 146389-62-0
MedChemExpress EUTBDSweden
To:
901 mgPOA
Go to cartEnquire
Description: Names: Zaragozic acid C; L-697350; Product Description: Zaragozic acid C (L-697350) is a potent sterol synthase inhibitor with potential antitumor activity. Zaragozic acid C contains multiple hydroxyl and alkyl substituents in its chemical structure, demonstrating complex functionalization capabilities. The synthesis of zaragozic acid C involves a photochemical C(sp3)-H acylation reaction, which resolves the challenging carbon substitution problem in the synthesis; Target: Endogenous Metabolite; CAS: 146389-62-0
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