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Details

Stereochemistry ABSOLUTE
Molecular Formula C55H86O24
Molecular Weight 1131.2569
Optical Activity UNSPECIFIED
Defined Stereocenters 27 / 27
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of .BETA.-ESCIN

SMILES

C\C=C(\C)C(=O)O[C@H]1[C@H](OC(C)=O)[C@]2(CO)[C@H](O)C[C@]3(C)C(=CC[C@@H]4[C@@]5(C)CC[C@H](O[C@@H]6O[C@@H]([C@@H](O[C@@H]7O[C@H](CO)[C@@H](O)[C@H](O)[C@H]7O)[C@H](O)[C@H]6O[C@@H]8O[C@H](CO)[C@@H](O)[C@H](O)[C@H]8O)C(O)=O)[C@](C)(CO)[C@@H]5CC[C@@]34C)[C@@H]2CC1(C)C

InChI

InChIKey=AXNVHPCVMSNXNP-OXPBSUTMSA-N
InChI=1S/C55H86O24/c1-10-23(2)46(71)79-43-44(72-24(3)60)55(22-59)26(17-50(43,4)5)25-11-12-30-51(6)15-14-32(52(7,21-58)29(51)13-16-53(30,8)54(25,9)18-31(55)61)75-49-41(77-48-38(67)36(65)34(63)28(20-57)74-48)39(68)40(42(78-49)45(69)70)76-47-37(66)35(64)33(62)27(19-56)73-47/h10-11,26-44,47-49,56-59,61-68H,12-22H2,1-9H3,(H,69,70)/b23-10-/t26-,27+,28+,29+,30+,31+,32-,33+,34+,35-,36-,37+,38+,39-,40-,41+,42-,43-,44-,47-,48-,49+,51-,52+,53+,54+,55-/m0/s1

HIDE SMILES / InChI

Molecular Formula C55H86O24
Molecular Weight 1131.2569
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 27 / 27
E/Z Centers 1
Optical Activity UNSPECIFIED

Aescin, the major active principle from Aesculus hippocastanum (Hippocastanaceae) the horse chestnut tree, has shown satisfactory evidence for a clinically significant activity in chronic venous insufficiency (CVI), haemorrhoids and post-operative oedema. In one controlled trial aescin was shown to be as effective as compression therapy as an alternative to medical treatment for CVI. The therapeutic benefit is well supported by a number of experimental investigations in different animal models, indicative of clearcut anti-oedematous, anti-inflammatory and venotonic properties, mainly related to the molecular mechanism of the agent, allowing improved entry of ions into channels, thus raising venous tension in both in vitro and in vivo conditions. Other mechanisms, i.e. release of PGF2 from veins, antagonism to 5-HT and histamine, reduced catabolism of tissue mucopolysaccharides, further underline the wide ranging mechanisms of the therapeutic activity of aescin. Aescin exists in two forms, α and β. β-aescin (b-escin) appears to be the active component of the mixture and is the molecular form present in major available pharmaceutical products. Beta-aescin has cytotoxic activity toward human colon adenocarcinoma cell lines.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: Q9Y4K0
Gene ID: 4017.0
Gene Symbol: LOXL2
Target Organism: Homo sapiens (Human)
35.0 µM [IC50]
Target ID: P00591
Gene ID: NA
Gene Symbol: PNLIP
Target Organism: Sus scrofa (Pig)
50.0 µM [IC50]
Target ID: P00591
Gene ID: NA
Gene Symbol: PNLIP
Target Organism: Sus scrofa (Pig)
Conditions
PubMed

PubMed

TitleDatePubMed
Escin Ia suppresses the metastasis of triple-negative breast cancer by inhibiting epithelial-mesenchymal transition via down-regulating LOXL2 expression.
2016-04-26
Comparative pharmacokinetics and the bioavailability of escin Ib and isoescin Ib following the administration of escin, pure escin Ib and isoescin Ib in rats.
2014-02-03
A liquid chromatography-tandem mass spectrometry method for the simultaneous quantification of escin Ia and escin Ib in human plasma: application to a pharmacokinetic study after intravenous administration.
2010-12
Anti-obesity effects of escins extracted from the seeds of Aesculus turbinata BLUME (Hippocastanaceae).
2008-01
Effects of alpha-escin on histomorphometrical parameters of long bones in rats with experimental post-steroid osteopenia.
2000-08-19
Influence of alpha-escin on the femoral bone strength in ovariectomized rats.
2000-05-19
[Substances contained in horse-chestnut seeds. 8. The acylaglycones of cryptoescin and alpha-escin].
1970-09
Patents

Sample Use Guides

Rats:The carried-out experiments indicated that the p.o. administration of 100 mg/kg of a-escin for 28 days to sexually mature male rats with experimental steroid-induced osteopenia caused slight protective action on bone tissue against unfavourable influence of prednisolone manifested by enhancement of mechanical features of femoral bone.
Route of Administration: Oral
Escin Ia (2.5, 5, 10 uM) obviously downregulated the LOXL2 mRNA expression and up-regulated the E-cadherin mRNA expression of MDA-MB-231 cells. In addition, MMP9 mRNA expression in MDA-MB-231 cells was moderately down-regulated by escin Ia (10 uM). treatment
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:17:08 GMT 2025
Edited
by admin
on Mon Mar 31 19:17:08 GMT 2025
Record UNII
QYK0D6H79O
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FLOGENCYL
Preferred Name English
.BETA.-ESCIN
MI  
Common Name English
ESCIN .BETA.-ESCIN [MI]
Common Name English
ESCIN IB (CONSTITUENT OF HORSE CHESTNUT) [DSC]
Common Name English
NSC-758653
Code English
.BETA.-ESCIN [MI]
Common Name English
.BETA.-AESCIN
Common Name English
BETA-ESCIN
Common Name English
ESCIN IB
Common Name English
.BETA.-D-GLUCOPYRANOSIDURONIC ACID, (3.BETA.,4.BETA.,16.ALPHA.,21.BETA.,22.ALPHA.)-22-(ACETYLOXY)-16,23,28-TRIHYDROXY-21-(((2Z)-2-METHYL-1-OXO-2-BUTEN-1-YL)OXY)OLEAN-12-EN-3-YL O-.BETA.-D-GLUCOPYRANOSYL-(1->2)-O-(.BETA.-D-GLUCOPYRANOSYL-(1->4))-
Systematic Name English
BETA-AESCIN
Common Name English
AESCIN B
Common Name English
Code System Code Type Description
WIKIPEDIA
beta-Escin
Created by admin on Mon Mar 31 19:17:08 GMT 2025 , Edited by admin on Mon Mar 31 19:17:08 GMT 2025
PRIMARY
EPA CompTox
DTXSID601026279
Created by admin on Mon Mar 31 19:17:08 GMT 2025 , Edited by admin on Mon Mar 31 19:17:08 GMT 2025
PRIMARY
MERCK INDEX
m5021
Created by admin on Mon Mar 31 19:17:08 GMT 2025 , Edited by admin on Mon Mar 31 19:17:08 GMT 2025
PRIMARY
CAS
11072-93-8
Created by admin on Mon Mar 31 19:17:08 GMT 2025 , Edited by admin on Mon Mar 31 19:17:08 GMT 2025
NO STRUCTURE GIVEN
CAS
26339-90-2
Created by admin on Mon Mar 31 19:17:08 GMT 2025 , Edited by admin on Mon Mar 31 19:17:08 GMT 2025
PRIMARY
NSC
758653
Created by admin on Mon Mar 31 19:17:08 GMT 2025 , Edited by admin on Mon Mar 31 19:17:08 GMT 2025
PRIMARY
SMS_ID
100000141345
Created by admin on Mon Mar 31 19:17:08 GMT 2025 , Edited by admin on Mon Mar 31 19:17:08 GMT 2025
PRIMARY
PUBCHEM
6476031
Created by admin on Mon Mar 31 19:17:08 GMT 2025 , Edited by admin on Mon Mar 31 19:17:08 GMT 2025
PRIMARY
FDA UNII
QYK0D6H79O
Created by admin on Mon Mar 31 19:17:08 GMT 2025 , Edited by admin on Mon Mar 31 19:17:08 GMT 2025
PRIMARY
RXCUI
1476
Created by admin on Mon Mar 31 19:17:08 GMT 2025 , Edited by admin on Mon Mar 31 19:17:08 GMT 2025
PRIMARY RxNorm
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