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Riligustilide is a chemical compound derived from the essential oil of Ligusticum chuanxiong, a traditional Chinese medicinal herb. It possesses a range of pharmacological properties, such as anti-inflammatory, analgesic, anti-cancer, and neuroprotective effects. Riligustilide has demonstrated potential in treating cardiovascular diseases, reducing blood pressure, and protecting against ischemic injury. Furthermore, it has shown anti-tumor effects by inhibiting the growth of cancer cells. As a result, riligustilide has emerged as a promising therapeutic agent for various health conditions, with ongoing research aimed at understanding its mechanisms and potential applications.

89354-45-0

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89354-45-0 Usage

Uses

Used in Pharmaceutical Industry:
Riligustilide is used as a therapeutic agent for cardiovascular diseases, as it has shown promising results in reducing blood pressure and protecting against ischemic injury.
Used in Oncology:
Riligustilide is used as an anti-cancer agent, as it has been found to inhibit the growth of cancer cells, making it a potential candidate for cancer treatment.
Used in Neurology:
Riligustilide is used as a neuroprotective agent, due to its ability to protect against neuronal damage and promote neuroprotection.
Used in Pain Management:
Riligustilide is used as an analgesic agent, as it possesses pain-relieving properties, making it a potential candidate for managing pain in various conditions.
Overall, Riligustilide's diverse range of pharmacological properties makes it a versatile compound with potential applications in various industries, including pharmaceuticals, oncology, neurology, and pain management. Further research is necessary to fully understand its mechanisms and maximize its potential as a therapeutic agent.

Check Digit Verification of cas no

The CAS Registry Mumber 89354-45-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,3,5 and 4 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 89354-45:
(7*8)+(6*9)+(5*3)+(4*5)+(3*4)+(2*4)+(1*5)=170
170 % 10 = 0
So 89354-45-0 is a valid CAS Registry Number.

89354-45-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (5aR,6S,7S,7aS,Z)-3-butylidene-6-propyl-3,4,5,5a,6,6',7a,7'-octahydro-1H,3'H-spiro[cyclobuta[e]isobenzofuran-7,1'-isobenzofuran]-1,3'-dione

1.2 Other means of identification

Product number -
Other names -

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:89354-45-0 SDS

89354-45-0Upstream product

89354-45-0Downstream Products

89354-45-0Relevant academic research and scientific papers

Triangeliphthalides A-D: Bioactive phthalide trimers with new skeletons from: Angelica sinensis and their production mechanism

Zou, Jian,Chen, Guo-Dong,Zhao, Huan,Wang, Xiao-Xia,Zhang, Zai-Jun,Qu, Yi-Bo,He, Rong-Rong,So, Kwok-Fai,Yao, Xin-Sheng,Gao, Hao

, p. 6221 - 6224 (2019)

Triangeliphthalides A-D (1-4), four novel phthalide trimers with two new linkage styles, were isolated from Angelica sinensis, together with two related phthalide dimers (5-6). Their structures including absolute configurations were determined. The production mechanism of phthalide polymers was proposed, and their bioactivities were also evaluated.

Triligustilides A and B: Two Pairs of Phthalide Trimers from Angelica sinensis with a Complex Polycyclic Skeleton and Their Activities

Zou, Jian,Chen, Guo-Dong,Zhao, Huan,Huang, Ying,Luo, Xiang,Xu, Wei,He, Rong-Rong,Hu, Dan,Yao, Xin-Sheng,Gao, Hao

, p. 884 - 887 (2018)

Two pairs of enantiomeric phthalide trimers [(-)/(+) triligustilides A (1a/1b) and (-)/(+) triligustilides B (2a/2b)] with complex polycyclic skeletons simultaneously possessing bridged, fused, and spiro ring systems were isolated from Angelica sinensis, together with two pairs of new phthalide dimers. The biogenetic pathways of new phthalides were proposed, and their bioactivities were also evaluated. This is the first time optically pure polymeric phthalides have been obtained from racemates, and their absolute configurations are reported.

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