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Steviolmonoside

HCID 21593622
NotesReactions
Basic informationNames & identifiersPropertiesChemistry & industryRelated reactionsCompound notes
Substructure searchFind similar structures

Basic information

CAS
60129-60-4
Standard SMILES
C=C1C[C@@]23CC[C@H]4[C@@](C)(CCC[C@@]4(C)C(=O)O)[C@@H]2CC[C@]1(O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)C3
InChIKey
QSIDJGUAAUSPMG-CULFPKEHSA-N
Molecular formula
C26H40O8
Average molar mass
480.6 g/mol
Monoisotopic mass
480.27231823

Names & identifiers

Preferred name
Steviolmonoside
IUPAC
(1R,4S,5R,9S,10R,13S)-5,9-dimethyl-14-methylidene-13-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxytetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid
English name
glucosilsteviol
Molecular formula
C26H40O8
Molecular weight
480.59

Names & synonyms

SteviolmonosideGlucosilsteviol60129-60-419-O-beta-D-Glucopyranosyl steviolFQY53Y3B5SCHEBI:145029DTXSID80975560(1R,4S,5R,9S,10R,13S)-5,9-dimethyl-14-methylidene-13-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxytetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acidKaur-16-en-18-oic acid, 13-(beta-D-glucopyranosyloxy)-, (4alpha)-(1R,4S,5R,9S,10R,13S)-5,9-dimethyl-14-methylidene-13-((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxytetracyclo(11.2.1.01,10.04,9)hexadecane-5-carboxylic acidRefChem:49956DTXCID001838751
Show more names
Steviol-monoside13-(β-D-Glucopyranosyloxy)kaur-16-en-18-oic acidKaur-16-en-18-oic acid, 13-(β-D-glucopyranosyloxy)-, (4α)-
Steviol-13-O-Glucoside13alpha-(beta-D-glucopyranosyloxy)-5beta,8alpha,9beta,10alpha-kaur-16-en-18-oic acidCCRIS 1517UNII-FQY53Y3B5Sorb1697095steviol-13-O-D-glucopyranosideSCHEMBL29379889QSIDJGUAAUSPMG-CULFPKEHSA-N

Properties

Computed structural properties

XLogP
2.2
Topological polar surface area
137 Ų
Hydrogen bond donors
5
Hydrogen bond acceptors
8
Rotatable bonds
4
Heavy atoms
34
Formal charge
0
Complexity
862

Physicochemical properties

Boiling point
666 · 666.0±55.0 °C(Predicted)
Density
1.34 · 1.34±0.1 g/cm3(Predicted)
pka
4.63 · 4.63±0.60(Predicted)
form
Solid
color
White to off-white
FDA UNII
53 Y3B5S · FQY53Y3B5S

Chemistry & industry

Applications

UsesSteviolmonoside (Glucosilsteviol) is a structural analogue of steviol. Steviolmonoside decreases glucose production and inhibits oxygen uptake in rat renal cortical tubules[1].

Suppliers23 total

成都普瑞法科技开发有限公司+86-028-82633397 18982077548 · [email protected]
銘瑞集團有限公司17318633522 · [email protected]
成都乐美天医药科技有限公司17308096051 17308096051 · [email protected]
武汉众志诚生物技术有限公司13628624121 13628604890 · [email protected]
成都普睿法药物研发有限公司82633860 18982077548 · [email protected]
浙江珲达生物科技有限公司0571-89903022 18679456698 · [email protected]
成都普思生物科技股份有限公司028-85370565-229 18080489829 · [email protected]
上海源叶生物科技有限公司13636370518 · [email protected]
北京百奥创新科技有限公司15522676233 · [email protected]
深圳振强药物研发有限公司0755-66853366 13670046396 · [email protected]
天津普西唐生物医药科技有限公司010-60605840 · [email protected]
武汉天植生物技术有限公司18607101326 15172504745 · [email protected]

Related reactions

1 records
New reaction record
HRID 1995145 reaction equation
HRID 1995145As reactantuspto-grants-1983_09

Compound notes

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On this pageBasic informationNames & identifiersPropertiesChemistry & industryRelated reactionsCompound notes

Database identifiers

CAS
60129-60-4
PubChem CID
21593622
DTXSID
DTXSID80975560
ChEBI
CHEBI:145029
UNII
FQY53Y3B5S
Nikkaji
J38.841F
成都标样生物科技有限公司028-81700200 13308200041 · [email protected]
威尔曼医药集团有限公司15807197853 18971451745 · [email protected]
Mensura Group Limited18780014153 · [email protected]
河南天孚化工有限公司+86-0371-55170693 +86-19937530512 · [email protected]
南京狄尔格医药科技有限公司025-025-51191215 18013836722 · [email protected]
成都普瑞法科技开发有限公司+86-28-82633860; +86-18080483897 · [email protected]
郑州艾克姆化工有限公司13303867194 · [email protected]
上海莫奇生物科技有限公司13341702378 · [email protected]
ANHUI BYERSEN BIOTECH CO. LTD+86-15385096007 +86-17755058861 · [email protected]
上海陶术生物科技股份有限公司+1-781-999-5354 · [email protected]
凌源贝卞森生物科技有限公司18642120371 · [email protected]
Additional notes · 1 item

DefinitionChEBI: Steviolmonoside is a beta-D-glucoside resulting from the formal condensation the tertiary allylic hydroxy group of steviol with beta-D-glucopyranose. It is a beta-D-glucoside, a monocarboxylic acid, a tetracyclic diterpenoid, a bridged compound, an ent-kaurane diterpenoid and a diterpene glycoside. It is functionally related to a steviol. It is a conjugate acid of a steviolmonoside(1-).