Description Chemical Properties Ingenol mebutate Pharmacokinetics & metabolism
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Ingenol

Description Chemical Properties Ingenol mebutate Pharmacokinetics & metabolism
Product Name
Ingenol
CAS No.
30220-46-3
Chemical Name
Ingenol
Synonyms
Ingeno;INGENOL;Inglenook;Ingenol, BR;(-)-Ingenol;Ingenol >99%;Ingenol base;Ingenol USP/EP/BP;INGENOL,HIGHPURITY;Ingenol 30220-46-3
CBNumber
CB4370581
Molecular Formula
C20H28O5
Formula Weight
348.43
MOL File
30220-46-3.mol
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Ingenol Property

Melting point:
153 °C
Boiling point:
523.8±50.0 °C(Predicted)
Density 
1.33±0.1 g/cm3(Predicted)
storage temp. 
Sealed in dry,Store in freezer, under -20°C
solubility 
DMSO: soluble
form 
film
pka
12.06±0.70(Predicted)
color 
colorless
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Safety

Hazard Codes 
Xi
Risk Statements 
38-41
Safety Statements 
26-36
WGK Germany 
3
HS Code 
2914409000
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H315Causes skin irritation

H318Causes serious eye damage

Precautionary statements

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

TCI Chemical
Product number
I1112
Product name
Ingenol
Packaging
10MG
Price
$158
Updated
2024/03/01
TCI Chemical
Product number
I1112
Product name
Ingenol
Packaging
50MG
Price
$475
Updated
2024/03/01
Cayman Chemical
Product number
14031
Product name
Ingenol
Purity
≥98%
Packaging
500μg
Price
$34
Updated
2024/03/01
Cayman Chemical
Product number
14031
Product name
Ingenol
Purity
≥98%
Packaging
1mg
Price
$59
Updated
2024/03/01
Cayman Chemical
Product number
14031
Product name
Ingenol
Purity
≥98%
Packaging
5mg
Price
$249
Updated
2024/03/01
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Ingenol Chemical Properties,Usage,Production

Description

Ingenol is a diterpenoid related to phorbol, derived from the milkweed plant E. peplus.1 It is a protein kinase C activator that displays a Ki value of 30 μM and an ED50 value of 27 μM in vitro. Most ingenol esters are tumor-promoting. However, ingenol mebutate possesses anti-tumor activity when used topically for actinic keratosis.

Chemical Properties

Isolated in 1968, ingenol, a highly oxygenated tetracyclic diterpene classified as a member of the phorboid family, is the parent compound of several dozen naturally occurring ingenanes that possess the same carbon skeleton but varied peripheral functionalities. In addition to their intriguing “inside-outside” bridged BC ring system, the ingenanes display interesting biological profiles that range from tumorpromoting to anti-leukemic and anti-HIV activities. Since the early 1980s, this combination of important biological function and complex architecture has inspired the efforts of numerous synthetic chemists.4 Previously, we reported an approach toward 1 wherein known â-ketoester 2 was advanced to diene 3, which served as a ring-closing metathesis substrate in a first generation Grubbs reaction that delivers the ingenane tetracycle 4.

Ingenol mebutate

Ingenol mebutate is a selective small-molecule activator of protein kinase C (PKC) isolated from the plant Euphorbia peplus with potential antineoplastic activity. Ingenol mebutate activates various protein kinase C (PKC) isoforms, thereby inducing apoptosis in some tumor cells, including myeloid leukemia cells, melanoma cells, and basal cell carcinoma cells. The PKC family consists of signaling isoenzymes that regulate many cell processes including proliferation, differentiation, and apoptosis.
Ingenol mebutate was approved by the FDA in January 2012, and it is marketed under the name Picato®. Picato gel is indicated for the topical treatment of actinic keratosis. Before approval, ingenol mebutate was called PEP005 as an investigational drug. PEP005 is a selective small molecule activator of protein kinase C (PKC) extracted from the plant Euphorbia peplus, whose sap has been used as a traditional medicine for the treatment of skin conditions including warts and cancer. PEP005 also has potent anti-leukemic effects, inducing apoptosis in myeloid leukemia cell lines and primary AML cells at nanomolar concentrations.
Ingenol mebutate gel (Picato) is a topical cream that the manufacturer is requesting to use as a secondline treatment in patients with actinic keratosis (AK) who have failed or are intolerant to 5-fluorouracil (5-FU). Ingenol mebutate gel is available in two strengths – a 0.015% dose for lesions on the face and scalp and a 0.05% dose for lesions on the trunk and extremities.

Pharmacokinetics & metabolism

The pharmacokinetics investigation of the systemic absorption of ingenol mebutate gel 0.05% was evaluated in a randomized vehicle-controlled double blind study, in which 1 g was applied to a contiguous 100 cm2 area of multiple AKs on the dorsal forearms of 16 patients in two consecutive daily applications. This clinical trial showed that there was no detectable systemic absorption of the parent drug or its two principal metabolites (both acyl isomers of ingenol mebutate), when the limit of detection was 0.1 ng/ml.
In vitro studies using [3H]-ingenol mebutate showed that metabolism of the drug by human hepatocytes is extensive. Other in vitro studies showed that ingenol mebutate neither induces human CYPP450 enzymes CYP1A2, 2C9 and 3A4a, nor inhibits CYP1A2, 2A6, 2B6, 2C8, 2C9, 2C19, 2D6, 2E1 and 3A4.

Description

Ingenol is a diterpenoid related to phorbol, derived from the milkweed plant E. peplus. It is a protein kinase C activator that displays a Ki value of 30 μM and an ED50 value of 27 μM in vitro. Most ingenol esters are tumor-promoting. However, ingenol mebutate possesses anti-tumor activity when used topically for actinic keratosis.

Uses

Ingenol, is the analogue of Ingenol 3-Angelate (I655800), which has anti-tumor activity when used topically for the treatment of actinic keratosis.

Definition

ChEBI: A tetracyclic diterpenoid that is 1a,2,5,5a,6,9,10,10a-octahydro-1H-2,8a-methanocyclopenta[a]cyclopropa[e][10]annulen-11-one substituted at positions 5, 5a and 6 by hydroxy groups, positions 1, 1, 7 and 9 by met yl groups, position 4 by a hydroxymethyl group and position 1 by an oxo group (the 1aR,2S,5R,5aR,6S,8aS,9R,10aR diastere mer).

Ingenol Preparation Products And Raw materials

Raw materials

Preparation Products

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View Lastest Price from Ingenol manufacturers

Baoji Guokang Bio-Technology Co., Ltd.
Product
Ingenol 30220-46-3
Price
US $1788.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
100kg
Release date
2021-06-08
Nanjing Sky Hope Tongyuan Biological Engineering Co., Ltd.
Product
Ingenol 30220-46-3
Price
US $400.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
10kg
Release date
2020-06-17
Shanghai Standard Technology Co., Ltd.
Product
Ingenol 30220-46-3
Price
US $0.00/mg
Min. Order
20mg
Purity
≥98%(HPLC)
Supply Ability
10 g
Release date
2020-04-07

30220-46-3, IngenolRelated Search:

CYCLOHEPTENE CYCLOOCTANONE Cyclooctane 2,2,4-TRIMETHYL-3-PENTANONE Cycloheptanone 1-NONEN-3-OL (R)-(-)-1-OCTEN-3-OL, 99 CYCLOOCTANEMETHANOL 3-BUTENE-1,2-DIOL ADOXAL 3,5-DIMETHYL-4-OCTANONE 2-TERT-BUTYLPROPANE-1,3-DIOL Ingenol 3,5-DIMETHYL-4-HEPTANONE CYCLOPROPYLACETALDEHYDE 1-HYDROXYMETHYL-3-CYCLOPENTENE 2,2-DIMETHYL-3-OCTANONE (HYDROXYMETHYL)CYCLOHEPTANE

  • 1A,2,5,5A,6,9,10,10A OCTAHYDRO-5,5A,6-TRIHYDROXY4(HYDROXYMETHYL)1,1,7,9-TETRAMETHYL1H-2,8 AMETHANOCYCLOPENTA[A]CYCLOPROPA[E]CYCLODECEN-11 ONE
  • 1 ALPHA,2,5,5 ALPHA,6,9,10,10 ALPHA-OCTAHYDRO-5,5 ALPHA,6-TRIHYDROXY-4-HYDROXYMETHYL-1,1,7,9-RETRAMETHYL-1H-2,8 ALPHA-M
  • INGENOL
  • INGENOL \ ACTIVATES PROTEIN KINASE C
  • (1ar,2s,5r,5ar,6s,8as,9r,10ar)-1a,2,5,5a,6,9,10,10a-octahydro-5,5a,6-trihydroxy-4-(hydroxymethyl)-1,1,7,9-tetramethyl-1h-2,8a-methanocyclopenta[a]cyclopropa[e]cyclodecen-11-one
  • INGENOL,HIGHPURITY
  • 1alpha,2,5,5alpha,6,9,10,10alpha-Octahydro-5,5alpha,6-trihydroxy-4-hydroxymethyl-1,1,7,9,-retramethyl-1H-2,8alpha-m
  • Ingenol 30220-46-3
  • HPLC 99% purity Ingenol from Euphorbia lathyris 30220-46-3
  • 99% Purity Ingenol Natural Plant Extracts 30220-46-3 Euphorbia Source
  • Ingenol, BR
  • (1aR,2S,8aS)-1aα,2,5,5a,6,9,10,10aα-Octahydro-5β,5aβ,6β-trihydroxy-4-(hydroxymethyl)-1,1,7,9α-tetramethyl-2,8aα-methano-1H-cyclopenta[a]cyclopropa[e]cyclodecene-11-one
  • (1aR,2S,8aS)-1aα,2,5,5a,6,9,10,10aα-Octahydro-5β,5aβ,6β-trihydroxy-4-hydroxymethyl-1,1,7,9α-tetramethyl-1H-2,8aα-methanocyclopenta[a]cyclopropa[e]cyclodecene-11-one
  • Ingenol >99%
  • Ingenol base
  • (1aR,2S,5R,5aR,6S,8aS,9R,10aR)-5,5a,6-Trihydroxy-4-(hydroxymethyl)-1,1,7,9-tetramethyl-1a,2,5,5a,6,9,10,10a-octahydro-1H-2,8a-methanocyclopenta[a]cyclopropa[e][10]annulen-11-one
  • 1H-2,8a-Methanocyclopenta[a]cyclopropa[e]cyclodecen-11-one,1a,2,5,5a,6,9,10,10a-octahydro-5,5a,6-trihydroxy-4-(hydroxyMethyl)-1,1,7,9-tetraMethyl-,(1aR,2S,5R,5aR,6S,8aS,9R,10aR)-
  • Ingenol USP/EP/BP
  • Inglenook
  • (-)-Ingenol
  • Ingeno
  • Giant Euphorbia Alcohol
  • (1S,4S,5R,6R,9S,10R,12R)-4,5,6-trihydroxy-7-(hydroxymethyl)-3,11,11,14-tetramethyltetracyclo[7.5.1.01,5.010,12]pentadeca-2,7-dien-15-one
  • 30220-46-3
  • BioChemical
  • Cell Signaling and Neuroscience
  • Cell Biology
  • Protein Phosphorylation
  • Protein Kinase Activators
  • Activator