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Details

Stereochemistry ABSOLUTE
Molecular Formula C16H22O11
Molecular Weight 390.3393
Optical Activity UNSPECIFIED
Defined Stereocenters 9 / 9
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MONOTROPEIN

SMILES

OC[C@H]1O[C@@H](O[C@@H]2OC=C([C@H]3C=C[C@](O)(CO)[C@@H]23)C(O)=O)[C@H](O)[C@@H](O)[C@@H]1O

InChI

InChIKey=HPWWQPXTUDMRBI-NJPMDSMTSA-N
InChI=1S/C16H22O11/c17-3-8-10(19)11(20)12(21)15(26-8)27-14-9-6(1-2-16(9,24)5-18)7(4-25-14)13(22)23/h1-2,4,6,8-12,14-15,17-21,24H,3,5H2,(H,22,23)/t6-,8-,9-,10-,11+,12-,14+,15+,16+/m1/s1

HIDE SMILES / InChI

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
PubMed

PubMed

TitleDatePubMed
Monotropein isolated from the roots of Morinda officinalis ameliorates proinflammatory mediators in RAW 264.7 macrophages and dextran sulfate sodium (DSS)-induced colitis via NF-κB inactivation.
2013-03
Iridoid glucosides with insecticidal activity from Galium melanantherum.
2007-10-05
[Studies on chemical constituents of in herb Pyrola calliatha].
2007-09
[Determination of monotropein in Radix Morindae from different processed products by HPLC].
2007-01
Antinociceptive anti-inflammatory effect of Monotropein isolated from the root of Morinda officinalis.
2005-10
Phenolic glycosides from Pyrola japonica.
2004-06
Hydrophilic carboxylic acids and iridoid glycosides in the juice of American and European cranberries (Vaccinium macrocarpon and V. oxycoccos), lingonberries (V. vitis-idaea), and blueberries (V. myrtillus).
2002-11-06
Sulfur-containing bis-iridoid glucosides and iridoid glucosides from Saprosmas cortechinii.
2002-05
Name Type Language
NSC-291303
Preferred Name English
MONOTROPEIN
MI  
Common Name English
CYCLOPENTA(C)PYRAN-4-CARBOXYLIC ACID, 1-(.BETA.-D-GLUCOPYRANOSYLOXY)-1,4A,7,7A-TETRAHYDRO-7-HYDROXY-7-(HYDROXYMETHYL)-, (1S-(1.ALPHA.,4A.ALPHA.,7.BETA.,7A.ALPHA.))-
Common Name English
NSC-88926
Code English
MONOTROPEIN [MI]
Common Name English
MONOTROPEINE
Common Name English
CYCLOPENTA(C)PYRAN-4-CARBOXYLIC ACID, 1-(.BETA.-D-GLUCOPYRANOSYLOXY)-1,4A,7,7A-TETRAHYDRO-7-HYDROXY-7-(HYDROXYMETHYL)-, (1S,4AS,7R,7AS)-
Common Name English
Code System Code Type Description
FDA UNII
0Y61M84O2T
Created by admin on Mon Mar 31 18:59:56 GMT 2025 , Edited by admin on Mon Mar 31 18:59:56 GMT 2025
PRIMARY
NSC
291303
Created by admin on Mon Mar 31 18:59:56 GMT 2025 , Edited by admin on Mon Mar 31 18:59:56 GMT 2025
PRIMARY
MERCK INDEX
m7613
Created by admin on Mon Mar 31 18:59:56 GMT 2025 , Edited by admin on Mon Mar 31 18:59:56 GMT 2025
PRIMARY Merck Index
PUBCHEM
73466
Created by admin on Mon Mar 31 18:59:56 GMT 2025 , Edited by admin on Mon Mar 31 18:59:56 GMT 2025
PRIMARY
NSC
88926
Created by admin on Mon Mar 31 18:59:56 GMT 2025 , Edited by admin on Mon Mar 31 18:59:56 GMT 2025
PRIMARY
CAS
5945-50-6
Created by admin on Mon Mar 31 18:59:56 GMT 2025 , Edited by admin on Mon Mar 31 18:59:56 GMT 2025
PRIMARY
EPA CompTox
DTXSID40974857
Created by admin on Mon Mar 31 18:59:56 GMT 2025 , Edited by admin on Mon Mar 31 18:59:56 GMT 2025
PRIMARY
CHEBI
6988
Created by admin on Mon Mar 31 18:59:56 GMT 2025 , Edited by admin on Mon Mar 31 18:59:56 GMT 2025
PRIMARY
MESH
C507582
Created by admin on Mon Mar 31 18:59:56 GMT 2025 , Edited by admin on Mon Mar 31 18:59:56 GMT 2025
PRIMARY