Andrographolide

ChemicalBook > CAS DataBase List > Andrographolide

Description References

Product Name: Andrographolide
CAS No.: 5508-58-7
Chemical Name: Andrographolide
Synonyms: ANDROGRAPHIS;ANDRO;ent-(3β,12E,14R)-3,14,19-Trihydroxy-8(17),12-labdadien-16,15-olide;Androg;raphoL;Andrograph;Neoandrogr;AndrographoL;rographolide;Andrographolid
CBNumber: CB1395576
Molecular Formula: C20H30O5
Formula Weight: 350.45
MOL File: 5508-58-7.mol

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Andrographolide Property

Melting point:: 229-232 °C (lit.)
alpha: -126 º (c=1.5,HAc)
Boiling point:: 557.3±50.0 °C(Predicted)
Density: d421 1.2317
storage temp.: 2-8°C
solubility: Soluble in DMSO (up to 25 mg/ml) or in Ethanol (up to 8 mg/ml).
pka: 12.36±0.20(Predicted)
form: Off-white solid
color: Off-white
optical activity: [α]20/D 126°, c = 1.5 in acetic acid
λmax: 223nm(MeOH)(lit.)
Merck: 14,633
BRN: 42762
Stability:: Stable for 2 years from date of purchsae as supplied. Solutions in DMSO or ethanol may be stored at -20°C for up to 3 months.
InChIKey: BOJKULTULYSRAS-QPSYGYIJSA-N
LogP: 0.424 (est)
CAS DataBase Reference: 5508-58-7

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Safety

Hazard Codes: Xn
Risk Statements: 20/21/22-36/37/38
Safety Statements: 22-24/25-36-26
WGK Germany: 3
RTECS: LU3490750
HS Code: 29322980

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Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H332Harmful if inhaled

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich

Product number: 172060
Product name: Andrographolide
Packaging: 50mg
Price: $85.2
Updated: 2024/03/01

Sigma-Aldrich

Product number: 1034862
Product name: Andrographolide
Purity: United States Pharmacopeia (USP) Reference Standard
Packaging: 50mg
Price: $529
Updated: 2024/03/01

TCI Chemical

Product number: A2459
Product name: Andrographolide
Purity: >98.0%(HPLC)
Packaging: 1g
Price: $33
Updated: 2024/03/01

TCI Chemical

Product number: A2459
Product name: Andrographolide
Purity: >98.0%(HPLC)
Packaging: 5g
Price: $95
Updated: 2024/03/01

Cayman Chemical

Product number: 11679
Product name: Andrographolide
Purity: ≥98%
Packaging: 50mg
Price: $20
Updated: 2024/03/01

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Andrographolide Chemical Properties,Usage,Production

Description

Andrographolide is the bitter principle, a colorless and neutral crystalline substance. It is the major labdane diterpenoid isolated from Andrographis paniculate. It exhibits antiviral, anti-inflammatory, and anticancer activities. The underlying mechanism is the inhibition of the mitogen-activated protein kinase/extracellular signal-regulated kinase (MAPK/ERK) signaling (specifically p38 MAPK/ERK1/2) pathway and downstream transcription factors such as nuclear factor kappa B (NF-κB) and nuclear factor of activated T cells (NFAT). Andrographolide is also confirmed with chemopreventive effects against and the inhibitory effects on cancer cell growth in breast, colon, epidermoid, gastric, liver, leukemia, myeloma, peripheral blood lymphocytes, and prostate cancers.
Andrographolide has been used for liver complaints and fever, and as an anti-inflammatory and immunostimulant. Andrographolide exerts anti-growth and pro-apoptotic effects on human rheumatoid arthritis fibroblast- like synoviocytes, the main cellular constituent of pannus, that combined with a massive infiltration of lymphocytes and macrophages, invades and destroys the local articular structure. Thereby, andrographolide is proposed to be used in Rheumatoid Arthritis and other autoimmune diseases.

References

[1] Mari?a A. Hidalgo, Juan L. Hancke, Juan C. Bertoglio and Rafael A. Burgos (2013) Andrographolide a New Potential Drug for the Long Term Treatment of Rheumatoid Arthritis Disease in book “Innovative Rheumatology”
[2] https://www.drugs.com/npp/andrographis.html
[3] Mitchell Low, Cheang S Khoo, Gerald Münch, Suresh Govindaraghavan, Nikolaus J Sucher (2014) An in vitro study of anti-inflammatory activity of standardised Andrographis paniculata extracts and pure andrographolide, BMC Complementary and Alternative Medicine, 15:18

Description

Andrographolide is a diterpene lactone compound extracted from Andrographis. paniculata (Burm. F) Nees. Andrographis paniculata is also known as lanhelian, yijianxi, zhanshecao, kucao, kudancao, etc. Since this product originates in India, it is also known as Indian grass. This product is dry ground part of Jupiteraceae plant Andrographis paniculata (conus) may originate in South Asia. It is commonly cultivated in China such as in Fujian, Guangdong, Hainan, Guangxi, and Yunnan and also in Australia and was also introduced in Jiangsu and Shaanxi.
Andrographis paniculata is commonly used in traditional Chinese medicine. Its ability of relieving “snake venom, and internal injuries cough” was recorded in “Lingnan herbal medicine records.” “Quanzhou Materia Medica” described it as “heat-clearing and detoxifying, anti-inflammatory, detumescence and inhibition throat inflammation, dysentery and high fever.”
The above ground part of Andrographis paniculata contains andrographolide, neo-andrographolide, 14-deoxygenated andrographolide, etc., and the root contains mainly flavonoids.

Chemical Properties

white square prism or flaky crystals (ethanol or methanol) and odorless, with a bitter taste. dissolved in boiling ethanol, slightly soluble in methanol or ethanol, very slightly soluble in chloroform, and almost insoluble in water. Since andrographolide has an ester structure, it is easy to hydrolysis, open loop and isomerization in the aqueous solution to affect the drug stability. At lower temperature, the stability of andrographolide is better; it is unstable in alkaline conditions, and its instability increased with the increase in alkaline strength. The most stable pH value is 3–5. Andrographolide is more stable in chloroform.

Occurrence

Andrographis is found growing wild in India and Sri Lanka and is cultivated in many other parts of the world.

History

In 1911, Gorter firstly isolated a crystalline substance from Andrographis paniculata, identified it as a diterpene lactone compound, and named it andrographolide .
Andrographolide structure is complex and difficult to artificially synthesize, so it is often extracted from the plant.
Andrographolide water solubility is poor and its bioavailability is low; its pharmacological effects are extensive but weak, so the preparation requirements are strict. Therefore, from the 1970s, drugs and organic chemical researchers have done a lot of work in the modification and transformation of andrographolide, mainly concentrated in the α, β-unsaturated lactone double bond Michael addition, redox, selective esterification of hydroxyl groups, oxidation and substitution reactions, intramolecular cyclization, replacement of lactone rings, etc. They had obtained a number of new derivatives. In the research of pharmacological effects, the main study of the andrographolide derivatives focuses on antitumor, antivirus, and other biological activities and has made some progress .

Uses

Andrographolide is a labdane diterpenoid. Andrographolide is the main bioactive component isolated from the medicinal plant Andrographis paniculata. It has a broad range of therapeutic applications including anti-inflammatory and anti-platelet aggregation activities and potential antineoplastic properties. Andrographolide showed significant antihepatotoxic action in P. berghei K173- induced hepatic damage in M. natalensis. Andrographolide inhibits tumor necrosis factor-α (TNF-α)-induced intercellular adhesion mol.-1 (ICAM-1) expression and adhesion of HL-60 cells onto human umbilical vein endothelial cells (HUVEC), which are associated with inflammatory diseases. These findings suggest that Andrographolide may have potential as a cardiovascular-protective agent.

Definition

ChEBI: Andrographolide is a labdane diterpenoid isolated from the leaves and roots of Andrographis paniculata that exhibits anti-HIV, anti-inflammatory and antineoplastic properties. It has a role as a metabolite, an anti-inflammatory drug, an anti-HIV agent and an antineoplastic agent. It is a gamma-lactone, a primary alcohol, a secondary alcohol, a labdane diterpenoid and a carbobicyclic compound.

Application

Andrographolide may be used as a reference standard for the determination of andrographolide in:
Leaves of Andrographis paniculata by soxhlet extraction-recrystallization-column chromatography purification followed by analyses using reversed phase high performance liquid chromatography (RP-HPLC) as well as gas chromatography-mass spectrometry (GC-MS).
Roots of Andrographis paniculata by HPLC with diode array detection (DAD), gas chromatography-mass spectrometry (GC-MS) and LC coupled to tandem mass spectrometry (MS/MS) equipped with electrospray ionization (ESI) and multiple reaction monitoring (MRM) mode of detection.
Stems of Andrographis paniculata by ultra-HPLC combined coupled to triple quadrupole-linear ion trap mass spectrometry (QqQLIT-ESI-MS/MS) with MRM detection.
Rat plasma samples by protein precipitation and subsequent ESI-LC-MS/MS determination using MRM detection.

General Description

Andrographolide, a bioactive diterpene lactone, is the main constituent of Andrographis paniculata, a plant used in traditional medicines. It is known to have different biological activities such as anti-inflammatory, anti-malarial, anti-cancer and hepatoprotective activity. It also shows potent anti-viral effect against dengue virus.

Biochem/physiol Actions

Diterpenoid lactone with anti-inflammatory properties. It blocks T-cell proliferation to allogenic stimuli and the chemotactic migration of macrophages induced by complement. Blocks the proliferation of several cancer cell lines in vitro.

Pharmacology

Modern pharmacological studies have shown that andrographolide has effects of anti-inflammatory, antibacterial, antivirus, antitumor, and immune regulation and can be used in treatment of cardiovascular-cerebrovascular diseases and protectionof the liver and gallbladder. Andrographolide can treat the fever caused by pneumococcus and hemolytic Streptococcus mutans, mainly by inhibiting the hypothalamus PGE2 and cAMP content to exert its antipyretic, nonetheless reducing the chemotaxis (fMLP) CD11b + and CD18 + may be the main mechanism of its antiinflammatory effect. Andrographolide has antagonistic effects on Hong Kong virus (HKV), Ebola virus (EBOV), and respiratory syncytial virus (RSV) and has been shown to inhibit HIV, SARS, and viral myocarditis ST2 in?vitro
Andrographolide can also ameliorate myocardial ischemia and serve as protection from ischemia-reperfusion injury. It also has protection effect of vascular endothelial cells as well as can regulate lipid disorder, lower blood pressure, and exert effect of anti-atherosclerosis. It can also prevent angiogenesis after restenosis and improve blood rheology. Its mechanisms are mainly due to its free radical scavenging and antiplatelet aggregation properties. Andrographolide can increase the bile flow, bile salt, bile acid, and deoxycholic acid in experimental rats and guinea pigs and can reverse the reduction of bile and cholic acid and other secretions caused by paracetamol and improve liver function .

Anticancer Research

It is a labdane diterpenoid, which shows cytotoxic effect against different cancercell lines like human epidermoid cancer cells (KB), lymphocytic leukemia cells(P388), breast cancer cells (MCF-7), and colon cancer cells (HCT-116). It inhibitsthe proliferation of colon cancer cells (HT-29) and exerts pro-differentiative effecton mouse myeloid leukemia M1 cell line (Desai et al. 2008).

Clinical Use

This product is commonly used clinically for dysentery, leptospirosis, meningitis, pneumonia, upper respiratory tract infection, and enhancing adrenal cortical function. In view of the requirement for clinical viral infection emergency, it is important to introduce the hydrophilic group in different lactone structure, enhance its water solubility, and improve efficacy. There are a variety kinds of andrographolide injection, including potassium dehydroandrograpolide succinate needle, potassium sodium dehydroandrographolide succinate needle. Lianbizhi is the representative of this class of drugs in current clinical application. Oral administration of andrographolide may induce bitter vomiting. Oral administration of this product and other preparations in large doses can cause epigastric discomfort and loss of appetite. It had been reported of drug eruption, upper abdominal pain, and anaphylactic shock caused by intramuscular injection. Severe symptom response emerged such as chest tightness, shortness of breath, pallor, lip bruising, cold sweats, weak pulse, decreased blood pressure, etc. Light reactions include abdominal pain, vomiting, asthma, urticaria, pimples, dizziness, head swelling, sneezing, chest pain, etc. The reaction is real time and also 5–20?min after injection and gradually improves 5–45?min after rescue and individual recovered by 24?h. There are also reports of acute amniotic fluid blockage caused by weaning lotion exchange. In addition, taking into account the adverse effects of andrographolide on reproduction, it is recommended to be used cautiously by fertility couples and pregnant women.

in vitro

andrographolide was found to suppress the expression of inducible nitric oxide synthase in a concentration-dependent manner. in the andrographolide-treated group, a reduction of akt, c-jun n-terminal kinase and p65 phosphorylation was observed. andrographolide also caused a decrease in bcl-2/nf-κb expression and a dose-dependent increase in the expression of cleaved-caspase3/bax protein [1].

in vivo

rats were dosed with andrographolide intragastrically for 5 consecutive days in a hepatoprotection study. results indicated that andrographolide could up-regulate glutamate cysteine ligase catalytic and modifier subunits, heme oxygenase-1, superoxide dismutase-1, glutathione s-transferase protein and mrna expression in the heart, liver, and kidney [2].

IC 50

11.0 ± 0.28 μg/ml for α-glucosidase; 11.3 ± 0.29 μg/ml for α-amylase

References

1) Xia et al. (2004), Andrographolide attenuates inflammation by inhibition of NF-kappa B activation through covalent modification of reduced cysteine 62 of p50; J. Immunol., 173 4207 2) Chen et al. (2004), Andrographolide suppresses endothelial cell apoptosis via activation of phosphatidyl inositol-3-kinase/Akt pathway; Biochem. Pharmacol., 67 1337 3) Yu et al. (2003), Antihyperglycemic effect of andrographolide is streptozotocin-induced diabetic rats; Planta Med., 69 1075

Andrographolide Preparation Products And Raw materials

Raw materials

Ethanol

Preparation Products

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View Lastest Price from Andrographolide manufacturers

Sinoway Industrial co., ltd.

Product: Andrographis Paniculata Extract / Andrographolide 5508-58-7
Price: US $0.00/KG
Min. Order: 2KG
Purity: 98%Andrographolide or Customized
Supply Ability: 20TONS
Release date: 2024-03-04

Hovane Phytochemicals Co., Ltd

Product: Andrographolide 5508-58-7
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Purity: 98%HPLC
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Release date: 2024-11-07

Wuhan Haorong Biotechnology Co.,Ltd

Product: Andrographolide 5508-58-7
Price: US $0.00-0.00/kg
Min. Order: 20kg
Purity: 99%
Supply Ability: 200000
Release date: 2023-08-15

5508-58-7, AndrographolideRelated Search:

ASTRAGALUS P.E. Andrographis Paniculata PE Mangiferin Icariin Asiaticoside ANDROGRAPHOLIDE, DEOXY- ANDROGRAPHOLIDE, DEHYDRO- ANDROGRAPHOLIDE, NEO-,ANDROGRAPHOLIDE, NEO(P) 1-Iodoadamantane DEHYDROANDROGRAPHOLIDESUCCINATE 14-DEOXY-11,12-DIDEHYDROANDROGRAPHOLIDE 5-METHYL-HEX-2-ENOIC ACID ETHYL ESTER DEHYDROANDROGRAPOLIDE SUCCINATE Andrographolide ANDROGRAPHOLIDE, DEOXY(SH) ANDROGRAPHOLIDE, DEHYDRO(P) ANDROGRAPHIS PANICULATA P.E./ ANDROGRAPHOLIDE ANDROGRAPHOLIDE, DEHYDRO(RG)

ent-(3β,12E,14R)-3,14,19-Trihydroxy-8(17),12-labdadien-16,15-olide

Andrographolide/Andrographis Paniculata P.E.

5-alpha,6-alpha,8a-alpha))-t

2(3h)-furanone,3-(2-(decahydro-6-hydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-met

3-(2-(Decahydro-6-hydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-methylene- 1-naphthalenyl)ethylidene)dihydro-4-hydroxy-, (1R-(1-alpha(E(S*)),4a-beta,5- alpha,6-alpha,8a-alpha))-2(3H)-furanone

(3E,4S)-3-[2-[(1R,4aS,5R,6R,8aS)-1,2,3,4,4a,5,6,7,8,8a-Decahydro-6-hydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-methylenenaphthalene-1-yl]ethylidene]dihydro-4-hydroxy-2(3H)-furanone

(S)-3-[(E)-2-[[(1R,4aα)-Decahydro-6β-hydroxy-5β-hydroxymethyl-5,8aβ-dimethyl-2-methylenenaphthalen]-1β-yl]ethylidene]dihydro-4-hydroxy-2(3H)-furanone

Andrographolid

Andrographolide (50 mg)

(3E,4S)-3-[2-[(1R,4aS,5R,6R,8aS)-Decahydro-6-hydroxy-5-(hydroxyMethyl)-5,8a-diMethyl-2-Methylene-1-naphthalenyl]ethylidene]dihydro-4-hydroxy-2(3H)-furanone

[1R-[1α[E(S*)],4aβ,5α,6α,8aα]]-3-[2-[Decahydro-6-hydroxy-5-(hydroxyMethyl)-5,8a-diMethyl-2-Methylene-1-naphthalenyl]ethylidene]dihydro-4-hydroxy-2(3H)-furanone

3α,14,15,18-Tetrahydroxy-5β,9βH,10α-labda-8(20),12-dien-16-oic Acid γ-Lactone

5.beta.,9.beta.h,10.alpha.-labda-8(20),12-dien-16-oic acid, 3.alpha.,14,15,18-tetrahydroxy-, .gamma.-lactone (8ci)

Rhizoma Sparganii

Androg

raphoL

ANDRO;ANDROGRAPHIS

Andrographolide 5508-58-7

Andrographolide - CAS 5508-58-7 - Calbiochem

Andrographis Herba

Andrographolide, 98%, from Andrographis paniculata

(3E)-3-[2-[(1R,8aS)-6-hydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-methylene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethylidene]-4-hydroxy-2-oxolanone

Andrographolides (Andrographis Paniculata Extract)

Andrographis Paniculata Extract Andrographolide

hylene-1-naphthalenyl)ethylidene)dihydro-4-hydroxy-,(1r-(1-alpha(e(s*)),4a-be

3-[2-[decahydro-6-hydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-methylenenaphthyl]ethylidene]dihydro-4-hydroxyfuran-2(3H)-one

2(3H)-Furanone, 3-2-(1R,4aS,5R,6R,8aS)-decahydro-6-hydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-methylene-1-naphthalenylethylidenedihydro-4-hydroxy-, (3E,4S)-

ANDROGRAPHOLIDE(P)

3-[2-[Decahydro-6-hydroyx-5-(hydroxymethyl)-5,8a-dimethyl-2-methylene-1-naphthalenylethylidene]dihydro-4-hydroxy-2(3H)-furanone

Andrographalide

ANDROGRAPHOLIDE:2(3H)-FURANONE,3-[2-[(1R,4AS,5R,6R,8AS)-DECAHYDRO-6-HYDROXY-5-(HYDROXYMETHYL)-5,8A-DIMETHYL-2-METHYLENE-1-NAPHTHALENYL]ETHYLIDENE]DIHYDRO-4-HYDROXY-, (3E,4S)-,

3A,14,15,18-TETRAHYDROXY-5B,9B,H,10A-LAMBDA-8,20-DIENE

2(3H)-FURANONE,3-[2-[(1R,4AS,5R,6R,8AS)-DECAHYDRO-6-HYDROXY-5-(HYDROXYMETHYL)-5,8A-DIMETHYL-2-METHYLENE-1-NAPHTHALENYL]ETHYLIDENE]DIHYDRO-4-HYDROXY-, (3E,4S)-

(3E,4S)-3-[2-[(1S,4aS,5R,6R,8aR)-6-Hydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-decalin-1-yl]ethylidene]-4-hydroxy-oxolan-2-one

ANDRO

ANDROGRAPHIS

ANDROGRAPHOLIDE

Andrographolide, froM Andrographis paniculata

(S,E)-4-Hydroxy-3-(2-((1R,4aS,5R,6R,8aS)-6-hydroxy-5-(hydroxyMethyl)-5,8a-diMethyl-2-Methylenedecahydronaphthalen-1-yl)ethylidene)dihydrofuran-2(3H)-one

Andrographis paniculata(Burm.f.)Nees

(3E,4S)-3-[2-[(1R,4aS,5R,6R,8aS)-6-hydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethylidene]-4-hydroxyoxolan-2-one

Andrographolide, 98%, from Andrographis paniculata (Burm. f.) Nees

Andrographis Extract (Standard)

Andrographolide CRS

Andrographolide &gt

Andrographolide powder

AndrographoL

Andrographis endolipid

Andrographolide USP/EP/BP

Andrographis extract/Andrographolide

Cotinus extract/lutein 98%

Andrographolide/ Andrographis

rographolide

Andrograpolide

(3E)-3-[2-[(1S,8aR)-6-hydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-decalin-1-yl]ethylidene]-4-hydroxy-oxolan-2-one

andrographolidume

Andrograph

Neoandrogr