Cas no 57282-82-3 (b-D-Glucopyranoside, (3b,25R)-spirost-5-en-3-ylO-6-deoxy-a-L-mannopyranosyl-(1®3)-O-[O-b-D-glucopyranosyl-(1®3)-6-deoxy-a-L-mannopyranosyl-(1®4)]-)
![b-D-Glucopyranoside, (3b,25R)-spirost-5-en-3-ylO-6-deoxy-a-L-mannopyranosyl-(1®3)-O-[O-b-D-glucopyranosyl-(1®3)-6-deoxy-a-L-mannopyranosyl-(1®4)]- structure](https://ossimg.kuujia.com/scimg/57500/57282-82-3x500.png)
57282-82-3 structure
Product Name:b-D-Glucopyranoside, (3b,25R)-spirost-5-en-3-ylO-6-deoxy-a-L-mannopyranosyl-(1®3)-O-[O-b-D-glucopyranosyl-(1®3)-6-deoxy-a-L-mannopyranosyl-(1®4)]-
CAS No:57282-82-3
MF:C51H82O21
MW:1031.18419885635
CID:382261
Update Time:2024-03-01
b-D-Glucopyranoside, (3b,25R)-spirost-5-en-3-ylO-6-deoxy-a-L-mannopyranosyl-(1®3)-O-[O-b-D-glucopyranosyl-(1®3)-6-deoxy-a-L-mannopyranosyl-(1®4)]- Chemical and Physical Properties
Names and Identifiers
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- 3)-6-deoxy-a-L-mannopyranosyl-(1®
- b-D-Glucopyranoside, (3b,25R)-spirost-5-en-3-ylO-6-deoxy-a-L-mannopyranosyl-(1®
- Pariphyllin A
- Spiro[8H-naphth[2',1':4,5]indeno[2,1-b]furan-8,2'-[2H]pyran],b-D-glucopyranoside deriv.
- Spirostan, b-D-glucopyranoside deriv.
- β-D-Glucopyranoside, (3β,25R)-spirost-5-en-3-yl O-6-deoxy-α-L-mannopyranosyl-(1→3)-O-[O-β-D-glucopyranosyl-(1→3)-6-deoxy-α-L-mannopyranosyl-(1→4)]-
- b-D-Glucopyranoside, (3b,25R)-spirost-5-en-3-ylO-6-deoxy-a-L-mannopyranosyl-(1®3)-O-[O-b-D-glucopyranosyl-(1®3)-6-deoxy-a-L-mannopyranosyl-(1®4)]-
-
- Inchi： 1S/C51H82O21/c1-20-9-14-51(63-19-20)21(2)32-29(72-51)16-28-26-8-7-24-15-25(10-12-49(24,5)27(26)11-13-50(28,32)6)66-48-41(62)44(71-45-38(59)36(57)33(54)22(3)64-45)42(31(18-53)68-48)69-47-40(61)43(34(55)23(4)65-47)70-46-39(60)37(58)35(56)30(17-52)67-46/h7,20-23,25-48,52-62H,8-19H2,1-6H3
- InChI Key： UCLYDZZDXSUIMC-UHFFFAOYSA-N
- SMILES： CC1C2(OCC(C)CC2)OC2CC3C(C12)(C)CCC1C3CC=C2C1(C)CCC(OC1C(O)C(OC3C(O)C(O)C(O)C(C)O3)C(OC3C(O)C(OC4C(O)C(O)C(O)C(CO)O4)C(O)C(C)O3)C(CO)O1)C2
b-D-Glucopyranoside, (3b,25R)-spirost-5-en-3-ylO-6-deoxy-a-L-mannopyranosyl-(1®3)-O-[O-b-D-glucopyranosyl-(1®3)-6-deoxy-a-L-mannopyranosyl-(1®4)]- Related Literature
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Andreas Nenning,Manuel Holzmann,Jürgen Fleig,Alexander K. Opitz Mater. Adv., 2021,2, 5422-5431
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Kay S. McMillan,Anthony G. McCluskey,Annette Sorensen,Marie Boyd,Michele Zagnoni Analyst, 2016,141, 100-110
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Dhirendra K. Chaudhary,Pramendra Kumar,Lokendra Kumar RSC Adv., 2016,6, 94731-94738
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Qiyuan Wu,Shangmin Xiong,Peichuan Shen,Shen Zhao,Alexander Orlov Catal. Sci. Technol., 2015,5, 2059-2064
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Amandine Altmayer-Henzien,Valérie Declerck,David J. Aitken,Ewen Lescop,Denis Merlet,Jonathan Farjon Org. Biomol. Chem., 2013,11, 7611-7615
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