1. Apoptosis
  2. Apoptosis
  3. Conophylline

Conophylline is a vinca alkaloid extracted from leaves of a tropical plant Ervatamia microphylla. Conophylline is a differentiation inducer of for pancreatic cells. Conophylline suppresses HSC and induces apoptosis.

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Conophylline Chemical Structure

Conophylline Chemical Structure

CAS No. : 142741-24-0

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Based on 1 publication(s) in Google Scholar

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Description

Conophylline is a vinca alkaloid extracted from leaves of a tropical plant Ervatamia microphylla. Conophylline is a differentiation inducer of for pancreatic cells. Conophylline suppresses HSC and induces apoptosis[1][2].

In Vitro

Conophylline (100 ng/ml; 48 hours) reproduces differentiationinducing activity but not apoptosis-inducing activity of activin[1].
? Conophylline (100 ng/ml; 72 hours) exhibits the differentiation-inducing activity in AR42J cells and converts these cells to endocrine cells[1].
? Conophylline increases the expression of neurogenin-3 by activating p38 mitogen-activated protein kinase to induce differentiation of AR42J cells[1].
? Conophylline reduces the expression of α-SMA and collagen-1 in rat HSC and Lx-2 cells[2].
? Conophylline inhibits DNA synthesis induced by serum[2].
? Conophylline also promots activation of caspase-3 and induces apoptosis in Lx-2 Cells[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Apoptosis Analysis[2]

Cell Line: Lx-2 Cells
Concentration: 12 hours
Incubation Time: 0.1 μg/ml
Result: Induced apoptosis

Western Blot Analysis[2]

Cell Line: Lx-2 cells
Concentration: 0.1 μg/ml
Incubation Time: 15 minutes, 30 minutes, 60 minutes, 120 minutes
Result: Increased phospho-JNK.
In Vivo

Conophylline (0.9 mg/kg; p.o.; daily; for 12 weeks) attenuates formation of the liver fibrosis induced by TAA in vivo[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Sprague-Dawley rats (70-80 g)[2]
Dosage: 0.9 mg/kg
Administration: Oral administration; daily; for 12 weeks
Result: Attenuated formation of the liver fibrosis induced by TAA.
Molecular Weight

794.89

Formula

C44H50N4O10

CAS No.
Appearance

Solid

Color

Off-white to light yellow

SMILES

CC[C@]1(C2)[C@@]3([H])[C@](C4=CC(O)=C5OC)(CCN3[C@@](C(C=C([C@]6(CCN7C[C@]8([H])[C@@]9([H])O8)[C@]7([H])[C@@]9(C%10)CC)C(NC6=C%10C(OC)=O)=C%11)=C%11O%12)([H])[C@@]%12([H])[C@H]1O)C(NC4=C5OC)=C2C(OC)=O

Structure Classification
Initial Source
Shipping

Room temperature in continental US; may vary elsewhere.

Storage
Powder -20°C 3 years
In solvent -80°C 6 months
-20°C 1 month
Purity & Documentation

Purity: ≥98.0%

References
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Conophylline
Cat. No.:
HY-N3619
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