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(S)-(+)-Camptothecin
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(S)-(+)-Camptothecin

CAS: 7689-03-4

Ref. 3D-FC15450

5g
189.00 €
10g
330.00 €
25g
672.00 €
50g
1,127.00 €
100g
2,130.00 €
Estimated delivery in United States, on Tuesday 14 Jan 2025

Product Information

Name:
(S)-(+)-Camptothecin
Synonyms:
  • (S)-4-Ethyl-4-hydroxy-1,12-dihydro-4H-2-oxa-6,12a-diaza-dibenzo[b,h]fluorene-3,13-dioneCamptothecine
  • (+)-Camptothecin
  • (4S)-4-Ethyl-4-hydroxy-1H-pyrano[3′,4′:6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione
  • (S)-Camptothecin
  • 1H-Pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione, 4-ethyl-4-hydroxy-, (4S)-
  • 1H-Pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione, 4-ethyl-4-hydroxy-, (S)-
  • 1H-Pyrano[3′,4′:6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione, 4-ethyl-4-hydroxy-, (4S)-
  • 1H-Pyrano[3′,4′:6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione, 4-ethyl-4-hydroxy-, (S)-
  • 20(S)-Camptothecin
  • 20(S)-Camptothecine
  • See more synonyms
  • 4-Ethyl-4-hydroxy-1H-pyrano-[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione
  • 4-Ethyl-4-hydroxy-1H-pyrano-[3,4:6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione
  • Campathecin
  • Campothecin
  • Camptothccin
  • Camptothecin, Camptotheca acuminata
  • Mag-Cpt
  • N-cyclohexyl-9-pentofuranosyl-9H-purin-6-amine
  • Nsc 94600
  • S-4-Ethyl-4-hydroxy-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione
  • S-Ckd 602
  • d-Camptothecin
  • Camptothecine
Description:

Camptothecin is a cytotoxic agent that has been shown to be effective against a variety of cancers. It is a natural product derived from the Chinese plant Camptotheca acuminata and has been used in the treatment of various cancers, including breast cancer, lung cancer, and colorectal cancer. Camptothecin forms protein complexes with DNA, which bind to the enzyme topoisomerase I and inhibit its activity. This results in DNA strand breaks during replication. It also binds to DNA by covalent bonds and inhibits transcription elongation by inhibiting the synthesis of RNA from DNA templates. The transition metal ion-dependent adducts formed with camptothecin have been shown to localize in subcellular organelles such as mitochondria, lysosomes, and endoplasmic reticulum. In vivo studies show that camptothecin can be detected by molecular imaging modalities such as positron emission tomography (PET) and

Notice:
Our products are intended for lab use only. For any other use, please contact us.
Brand:
Biosynth
Long term storage:
Notes:

Chemical properties

Molecular weight:
348.35 g/mol
Formula:
C20H16N2O4
Purity:
Min. 98 Area-%
Color/Form:
Yellow Powder
MDL:
Melting point:
Boiling point:
Flash point:
Density:
Concentration:
EINECS:
Merck:
HS code:

Hazard Info

UN Number:
EQ:
Class:
H Statements:
P Statements:
Forbidden to fly:
Hazard Info:
Packing Group:
LQ:

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