(S) -10-Hydroxycamptothecin-d5(S) -10-Hydroxycamptothecin-d5 - High-quality laboratory reagent available from Gentaur. Catalog: 804-HY-N0095S-01.804-HY-N0095S-01804-HY-N0095S-01Business & Industrial > Science & Laboratory(S) -10-Hydroxycamptothecin-d5
Gentaur
EUR12027-02-20

(S) -10-Hydroxycamptothecin-d5

CAT:
804-HY-N0095S-01
Size:
1 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
(S) -10-Hydroxycamptothecin-d5 - image 1

(S) -10-Hydroxycamptothecin-d5

  • Description:

    (S) -10-Hydroxycamptothecin-d5 (10-HCPT-d5) is the deuterium labeled (S) -10-Hydroxycamptothecin. (S) -10-Hydroxycamptothecin (10-HCPT) is a DNA topoisomerase I inhibitor. (S) -10-Hydroxycamptothecin exhibits a remarkable apoptosis-inducing effect. (S) -10-Hydroxycamptothecin has the potential for hepatoma, gastric carcinoma, colon cancer and leukaemia research[1][2][3][4].
  • Product Name Alternative:

    10-HCPT-d5; 10-Hydroxycamptothecin-d5
  • UNSPSC:

    12352005
  • Target:

    Apoptosis; Isotope-Labeled Compounds; Topoisomerase
  • Related Pathways:

    Apoptosis; Cell Cycle/DNA Damage; Others
  • Applications:

    Cancer-programmed cell death
  • Field of Research:

    Cancer
  • Solubility:

    10 mM in DMSO
  • Smiles:

    O=C1N2C(C=3C(C2)=CC=4C(N3)=CC=C(O)C4)=CC5=C1COC(=O)[C@@]5(C(C([2H])([2H])[2H])([2H])[2H])O
  • Molecular Formula:

    C20H11D5N2O5
  • Molecular Weight:

    369.38
  • References & Citations:

    [1]Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53 (2) :211-216.|[2]Min Liu, et al. Intracellular delivery of 10-hydroxycamptothecin with targeted nanostructured lipid carriers against multidrug resistance . Journal of Drug Targeting.|[3]Min Liu, et al. Intracellular delivery of 10-hydroxycamptothecin with targeted nanostructured lipid carriers against multidrug resistance. J Drug Target, Early Online: 1–8|[4]Yu P, et al. Synthesis and preliminary anticancer evaluation of 10-hydroxycamptothecin analogs. Biol Pharm Bull. 2012;35 (8) :1295-9.|[5]Zhang XW, et al. Differentiation-inducing action of 10-hydroxycamptothecin on human hepatoma Hep G2 cells. Acta Pharmacol Sin. 2000 Apr;21 (4) :364-8.|[6]Zhang XW, et al. Differential regulation of P53, c-Myc, Bcl-2, Bax and AFP protein expression, and caspase activity during 10-hydroxycamptothecin-induced apoptosis in Hep G2 cells. Anticancer Drugs. 2000 Oct;11 (9) :747-56.|[7]Liu M, et al. Intracellular delivery of 10-hydroxycamptothecin with targeted nanostructured lipid carriers against multidrug resistance. J Drug Target. 2016;24 (5) :433-40.
  • Shipping Conditions:

    Room temperature
  • Scientific Category:

    Isotope-Labeled Compounds
  • Clinical Information:

    No Development Reported
  • CAS Number:

    [1330277-66-1]