Monomelittoside

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C15H22O10
Molecular Weight	362.3292
Optical Activity	( - )
Defined Stereocenters	9 / 9
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

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

InChI

InChIKey=WVHRUHMGDQLMBZ-KRWIWSHESA-N

InChI=1S/C15H22O10/c16-4-6-3-8(18)15(22)1-2-23-13(9(6)15)25-14-12(21)11(20)10(19)7(5-17)24-14/h1-3,7-14,16-22H,4-5H2/t7-,8-,9+,10-,11+,12-,13+,14+,15-/m1/s1

HIDE SMILES / InChI

Approval Year

PubMed

Title	Date	PubMed
Secoiridoids and other chemotaxonomically relevant compounds in Pedicularis: phytochemical analysis and comparison of Pedicularis rostratocapitata Crantz and Pedicularis verticillata L. from Dolomites.	2016-08	26828611
Iridoids and phenylethanoid from Pedicularis kerneri Dalla Torre growing in Dolomites, Italy.	2016	26207992
Reassessment of Melittis melissophyllum L. subsp. melissophyllum iridoidic fraction.	2016	26131916
Iridoid glycoside constituents of Stachys lanata.	2008-10	18788778
Monoterpenoids from Stachys glutinosa L.	2006-05-20	16835100
A new phenylethanoid glycoside from Clerodendrum inerme.	2005-10	16259134
Iridoid and bisiridoid glycosides from Globularia cordifolia.	2003-07-23	12872925
Iridoids from Stachys grandidentata (Labiatae).	2001-11-29	11724403

Name

Type

Language

Monomelittoside

Common Name

English

(1S,4aS,5R,7aR)-1,4a,5,7a-Tetrahydro-4a,5-dihydroxy-7-(hydroxymethyl)cyclopenta[c]pyran-1-yl ?-D-glucopyranoside

Preferred Name

English

?-D-Glucopyranoside, 1,4a,5,7a-tetrahydro-4a,5-dihydroxy-7-(hydroxymethyl)cyclopenta[c]pyran-1-yl, [1S-(1?,4a?,5?,7a?)]-

Systematic Name

English

?-D-Glucopyranoside, (1S,4aS,5R,7aR)-1,4a,5,7a-tetrahydro-4a,5-dihydroxy-7-(hydroxymethyl)cyclopenta[c]pyran-1-yl

Systematic Name

English

Code System Code Type Description

FDA UNII

SFW5FJ6LXU

Created by admin on Wed Apr 02 19:42:28 GMT 2025 , Edited by admin on Wed Apr 02 19:42:28 GMT 2025

PRIMARY

PUBCHEM

11968396

Created by admin on Wed Apr 02 19:42:28 GMT 2025 , Edited by admin on Wed Apr 02 19:42:28 GMT 2025

PRIMARY

CAS

20633-72-1

Created by admin on Wed Apr 02 19:42:28 GMT 2025 , Edited by admin on Wed Apr 02 19:42:28 GMT 2025

PRIMARY

SUBSTANCE RECORD


					SFW5FJ6LXU

Monomelittoside