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Sappanchalcone is a member of the chalcone class, characterized by a trans-chalcone structure with hydroxy groups at positions 3, 4, and 4', and a methoxy group at position 2'. It is a yellow solid that can be isolated from Caesalpinia sappan and has been found to possess neuroprotective and cytoprotective activities.

94344-54-4

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94344-54-4 Usage

Uses

Used in Pharmaceutical Industry:
Sappanchalcone is used as a neuroprotective agent for its ability to protect neurons and support the health of the nervous system. Its cytoprotective properties also make it a potential candidate for the development of treatments aimed at preserving cell integrity and function.
Used in Research Applications:
In the field of scientific research, sappanchalcone serves as a valuable compound for studying the mechanisms of neuroprotection and cytoprotection. Its isolation from Caesalpinia sappan provides a natural source for investigating the therapeutic potential of plant-derived compounds in various diseases and conditions affecting the nervous system and cellular health.

Check Digit Verification of cas no

The CAS Registry Mumber 94344-54-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,3,4 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 94344-54:
(7*9)+(6*4)+(5*3)+(4*4)+(3*4)+(2*5)+(1*4)=144
144 % 10 = 4
So 94344-54-4 is a valid CAS Registry Number.
InChI:InChI=1/C16H14O5/c1-21-16-9-11(17)4-5-12(16)13(18)6-2-10-3-7-14(19)15(20)8-10/h2-9,17,19-20H,1H3/b6-2+

94344-54-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name sappanchalcone

1.2 Other means of identification

Product number -
Other names 3,4,4'-Trihydroxy-2'-methoxychalcone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:94344-54-4 SDS

94344-54-4Downstream Products

94344-54-4Relevant academic research and scientific papers

Synthesis and evaluation of butein derivatives for in vitro and in vivo inflammatory response suppression in lymphedema

Kang, Hee,Ku, Jin-Mo,Lee, Jung-hun,Lee, Sukchan,Park, Kye Won,Roh, Kangsan,Song, Youngju

, (2020/05/01)

Herein, we demonstrate that butein (1) can prevent swelling in a murine lymphedema model by suppressing tumor necrosis factor α (TNF-α) production. Butein derivatives were synthesized and evaluated to identify compounds with in vitro anti-inflammatory activity. Among them, 20 μM of compounds 7j, 7m, and 14a showed 50percent suppression of TNF-α production in mouse peritoneal macrophages after lipopolysaccharide stimulation. Compound 14a, exhibited the strongest potency with an in vitro IC50 of 14.6 μM and suppressed limb volume by 70percent in a murine lymphedema model. The prodrug strategy enabled a six-fold increase in kinetic solubility of compound 1 and five-fold higher levels of active metabolite in the blood for compound 14a via oral administration in the pharmacokinetics study. We suggest that the compound 14a could be developed as a potential therapeutic agent targeting anti-inflammatory activity to alleviate lymphedema progression.

USE OF THE EXTRACT OF CAESALPINIA SAPPAN L. AND COMPOUNDS THEREFROM

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Page/Page column 26-27, (2008/06/13)

The present invention relates to an extract of Caesalpinia sappan L. having an angiogenesis inhibition activity and a use of the compound isolated therefrom, more precisely an extract of Caesalpinia sappan L. extracted by using water, alcohol or a mixture thereof , and a use of brazilin, sappanchalcone and brazilein isolated from the extract as an angiogenesis inhibitor. The extract of Caesalpinia sappan L. of the invention and a compound isolated therefrom have angiogenesis inhibition activity, so that they can be effectively used for the prevention and treatment of angiogenesis associated diseases such as vascular diseases, cardiovascular diseases, ophthalmic diseases, chronic inflammatory diseases, dermatological diseases, Alzheimer's disease, obesity and cancer.

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