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Details

Stereochemistry ABSOLUTE
Molecular Formula C55H85O24.Na
Molecular Weight 1153.2388
Optical Activity UNSPECIFIED
Defined Stereocenters 27 / 27
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of .ALPHA.-ESCIN SODIUM

SMILES

[Na+].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=YFQNXDPEDQNIMQ-LHSNRORRSA-M
InChI=1S/C55H86O24.Na/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);/q;+1/p-1/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 Na
Molecular Weight 22.98976928
Charge 1
Count
MOL RATIO 1 MOL RATIO (average)
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C55H85O24
Molecular Weight 1130.249
Charge -1
Count
MOL RATIO 1 MOL RATIO (average)
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 27 / 27
E/Z Centers 1
Optical Activity UNSPECIFIED

Description

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

Primary TargetPharmacologyConditionPotency
35.0 µM [IC50]
50.0 µM [IC50]

Conditions

ConditionModalityTargetsHighest PhaseProduct
Secondary
Unknown
Primary
Unknown
Primary
Unknown
Primary
Unknown
Primary
Unknown
Primary
Unknown
Primary
Unknown

PubMed

Sample Use Guides

In Vivo Use Guide
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
In Vitro Use Guide
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
Record UNII
58G9ZMJ34D
Record Status Validated (UNII)
Record Version