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Licoricidin, a natural compound derived from licorice root, exhibits a range of biological activities, including anti-inflammatory, antiviral, and anticancer properties. Its diverse therapeutic potential makes it a compound of interest for various medical applications.

30508-27-1

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Basic information
1. Product Name: licoricidin
2. Synonyms: licoricidin;7-O-Demethyllicorisoflavan A;Licorisoflavan B;1,3-Benzenediol,4-[(3R)-3,4-dihydro-7-hydroxy-5-methoxy-6-(3-methyl-2-buten-1-yl)-2H-1-benzopyran-3-yl]-2-(3-methyl-2-buten-1-yl)-
3. CAS NO:30508-27-1
4. Molecular Formula: C26H32O5
5. Molecular Weight: 424.52928
6. EINECS: N/A
7. Product Categories: N/A
8. Mol File: 30508-27-1.mol
Chemical Properties
1. Melting Point: 161.0-162.5℃
2. Boiling Point: 610.8°Cat760mmHg
3. Flash Point: 323.2°C
4. Appearance: /
5. Density: 1.171g/cm³
6. Vapor Pressure: 1.63E-15mmHg at 25°C
7. Refractive Index: 1.597
8. Storage Temp.: N/A
9. Solubility: N/A
10. PKA: 10.10±0.40(Predicted)
11. CAS DataBase Reference: licoricidin(CAS DataBase Reference)
12. NIST Chemistry Reference: licoricidin(30508-27-1)
13. EPA Substance Registry System: licoricidin(30508-27-1)
Safety Data
1. Hazard Codes: N/A
2. Statements: N/A
3. Safety Statements: N/A
4. WGK Germany:
5. RTECS:
6. HazardClass: N/A
7. PackingGroup: N/A
8. Hazardous Substances Data: 30508-27-1(Hazardous Substances Data)

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SDS
Synthetic route
Upstream product
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30508-27-1 Usage

Uses

Used in Anticancer Applications:
Licoricidin is used as an anticancer agent for its ability to inhibit the growth of various cancer cell lines, such as breast cancer, lung cancer, and leukemia. Its mechanism of action involves targeting multiple signaling pathways and cellular processes, making it a promising candidate for cancer therapy.
Used in Antiviral Applications:
In the field of antiviral therapy, licoricidin is used as an antiviral agent, particularly against HIV-1 and influenza virus. Its antiviral activity is attributed to its ability to interfere with viral replication and entry into host cells, offering a potential therapeutic strategy for viral infections.
Used in Anti-inflammatory Applications:
Licoricidin is utilized as an anti-inflammatory agent due to its capacity to suppress the production of pro-inflammatory cytokines. This property makes it a potential treatment for inflammatory diseases, where reducing inflammation can alleviate symptoms and prevent disease progression.

Check Digit Verification of cas no

The CAS Registry Mumber 30508-27-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,5,0 and 8 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 30508-27:
(7*3)+(6*0)+(5*5)+(4*0)+(3*8)+(2*2)+(1*7)=81
81 % 10 = 1
So 30508-27-1 is a valid CAS Registry Number.

InChI:InChI=1/C26H32O5/c1-15(2)6-8-19-22(27)11-10-18(25(19)29)17-12-21-24(31-14-17)13-23(28)20(26(21)30-5)9-7-16(3)4/h6-7,10-11,13,17,27-29H,8-9,12,14H2,1-5H3/t17-/m0/s1

30508-27-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name	licoricidin

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:30508-27-1 SDS

30508-27-1Synthetic route

: 30508-27-1
(+)-(R)-licoricidin

: 77-78-1
dimethyl sulfate

: 6-[(R)-5,7-Dimethoxy-6-(3-methyl-but-2-enyl)-chroman-3-yl]-3-methoxy-2-(3-methyl-but-2-enyl)-phenol

Conditions

Conditions	Yield
With potassium carbonate In acetone

: 108-24-7
acetic anhydride

: 30508-27-1
(+)-(R)-licoricidin

: (+)-(R)-licoricidin triacetate

Conditions

Conditions	Yield
In pyridine

: 30508-27-1
(+)-(R)-licoricidin

A: 6-((R)-5-Methoxy-8,8-dimethyl-3,4,7,8-tetrahydro-2H,6H-pyrano[3,2-g]chromen-3-yl)-2,2-dimethyl-chroman-5-ol

B: 8-((R)-5-Methoxy-8,8-dimethyl-3,4,7,8-tetrahydro-2H,6H-pyrano[3,2-g]chromen-3-yl)-2,2-dimethyl-chroman-5-ol

Conditions

Conditions	Yield
With hydrogenchloride In methanol

: 30508-27-1
(+)-(R)-licoricidin

: 1346768-14-6
4',7-dihydroxy-5-methoxy-6,3'-diprenylisoflavanquinone

Conditions

Conditions	Yield
With sodium hydroxide In ethanol for 2h;

: 30508-27-1
(+)-(R)-licoricidin

: C30H34O7

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: pyridine / 16 h 2: palladium dichloride / ethanol; water / 48 h / 20 °C View Scheme

: 30508-27-1
(+)-(R)-licoricidin

A: 1006718-45-1
1-methoxyerythrabyssin II

B: 1551035-71-2
licorisoflavan D

Conditions

Conditions	Yield
With 2,3-dicyano-5,6-dichloro-p-benzoquinone In benzene for 0.0833333h; Reflux;	A 1 mg B 9.9 mg

: 30508-27-1
(+)-(R)-licoricidin

A: 1551035-46-1
licorisoflavan C

B: 1551035-71-2
licorisoflavan D

C: licorisoflavan E

Conditions

Conditions	Yield
With palladium dichloride In ethanol at 20℃; for 4h;	A 5.2 mg B 3.2 mg C 7.6 mg

: 30508-27-1
(+)-(R)-licoricidin

: licorisoflavan E

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: pyridine / 16 h 2: palladium dichloride / ethanol; water / 48 h / 20 °C 3: sodium hydroxide; water / 0.5 h View Scheme