VindolineVindoline - High-quality laboratory reagent available from Gentaur. Catalog: 804-HY-N0687-01.804-HY-N0687-01804-HY-N0687-01Business & Industrial > Science & LaboratoryVindoline
Gentaur
EUR12027-02-22

Vindoline

CAT:
804-HY-N0687-01
Size:
5 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Vindoline - image 1

Vindoline

  • Description:

    Vindoline is an orally active vinca alkaloid. Vindoline can be extracted from the leaves of Catharanthus roseus. Vindoline has a weak inhibitory effect on the self-assembly of tubulin. Vindoline alleviates Apoptosis, inhibits p-p65 and p-ERK. Vindoline improves diabetes, bone loss, osteoarthritis, and kidney damage[1][2][3][4][5].
  • UNSPSC:

    12352005
  • Hazard Statement:

    H302, H315, H319, H335
  • Target:

    Apoptosis; Microtubule/Tubulin; NF-κB; PERK
  • Type:

    Natural Products
  • Related Pathways:

    Apoptosis; Cell Cycle/DNA Damage; Cytoskeleton; NF-κB
  • Applications:

    Cancer-programmed cell death
  • Field of Research:

    Endocrinology; Metabolic Disease; Inflammation/Immunology
  • Assay Protocol:

    https://www.medchemexpress.com/vindoline.html
  • Concentration:

    10mM
  • Purity:

    99.95
  • Solubility:

    DMSO : 250 mg/mL (ultrasonic)
  • Smiles:

    CC[C@@]1(C=CCN2CC3)[C@@]2([H])[C@@]3(C4=CC=C(OC)C=C4N5C)[C@]5([H])[C@](C(OC)=O)(O)[C@@H]1OC(C)=O
  • Molecular Formula:

    C25H32N2O6
  • Molecular Weight:

    456.53
  • Precautions:

    H302, H315, H319, H335
  • References & Citations:

    [1]Prakash V, et al. Mechanism of interaction of vinca alkaloids with tubulin: catharanthine and vindoline. Biochemistry. 1991 Jan 22;30 (3) :873-80.|[2]Yao XG, et al. Natural product vindoline stimulates insulin secretion and efficiently ameliorates glucose homeostasis in diabetic murine models. J Ethnopharmacol. 2013 Oct 28;150 (1) :285-97.|[3]Zhan Y, et al. Vindoline Inhibits RANKL-Induced Osteoclastogenesis and Prevents Ovariectomy-Induced Bone Loss in Mice. Front Pharmacol. 2020 Jan 22;10:1587.|[4]Wang Z, et al. Vindoline mitigates cisplatin-mediated kidney damage by alleviating redox imbalance, apoptosis and inflammation through extracellular signal-regulated kinase pathway modulation. J Physiol Pharmacol. 2024 Dec;75 (6) .|[5]Zhu M, et al. Vindoline Attenuates Osteoarthritis Progression Through Suppressing the NF-κB and ERK Pathways in Both Chondrocytes and Subchondral Osteoclasts. Front Pharmacol. 2022 Jan 12;12:764598.
  • Shipping Conditions:

    Room Temperature
  • Storage Conditions:

    4°C (Powder, protect from light)
  • Scientific Category:

    Natural Products
  • Clinical Information:

    No Development Reported
  • CAS Number:

    [2182-14-1]