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C9911

Sigma-Aldrich

(S)-(+)-Camptothecin

≥90% (HPLC), powder, DNA topoisomerase I inhibitor

Sinonimo/i:

(S)-4-Ethyl-4-hydroxy-1H-pyrano-[3′,4′:6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione

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250 MG
CHF 297.00
100 MG
CHF 373.00
1 G
CHF 771.00

CHF 297.00


Spedizione prevista il26 marzo 2025


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Cambia visualizzazione
250 MG
CHF 297.00
100 MG
CHF 373.00
1 G
CHF 771.00

About This Item

Formula empirica (notazione di Hill):
C20H16N2O4
Numero CAS:
Peso molecolare:
348.35
Beilstein:
631069
Numero MDL:
Codice UNSPSC:
12352200
ID PubChem:
NACRES:
NA.77

CHF 297.00


Spedizione prevista il26 marzo 2025


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Nome del prodotto

(S)-(+)-Camptothecin, ≥90% (HPLC), powder

Livello qualitativo

Saggio

≥90% (HPLC)

Stato

powder

Punto di fusione

260 °C (dec.) (lit.)

Solubilità

chloroform/methanol (4:1): 5 mg/mL

Spettro attività antibiotica

neoplastics

Modalità d’azione

DNA synthesis | interferes
enzyme | inhibits

Temperatura di conservazione

2-8°C

Stringa SMILE

CC[C@@]1(O)C(=O)OCC2=C1C=C3N(Cc4cc5ccccc5nc34)C2=O

InChI

1S/C20H16N2O4/c1-2-20(25)14-8-16-17-12(7-11-5-3-4-6-15(11)21-17)9-22(16)18(23)13(14)10-26-19(20)24/h3-8,25H,2,9-10H2,1H3/t20-/m0/s1
VSJKWCGYPAHWDS-FQEVSTJZSA-N

Informazioni sul gene

human ... TOP1(7150)
mouse ... Prkca(18750)
rat ... Sstr2(54305)

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Azioni biochim/fisiol

(S)-(+)-Camptothecin binds irreversibly to the DNA-topoisomerase I complex, inhibiting the reassociation of DNA after cleavage by topoisomerase I and traps the enzyme in a covalent linkage with DNA. The enzyme complex is ubiquinated and destroyed by the 26S proteasome, thus depleting cellular topoisomerase I. Blocks the cell cycle in S-phase at low does and induces apoptosis in a large number of normal and tumor cell lines by cell cycle-dependent and cell cycle-independent processes.

Caratteristiche e vantaggi

This compound is a featured product for Apoptosis research. Click here to discover more featured Apoptosis products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.

Altre note

20S isomer

Pittogrammi

Skull and crossbonesHealth hazard

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Acute Tox. 3 Oral - Muta. 1B

Codice della classe di stoccaggio

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


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Articoli

We presents an article on Autophagy in Cancer Promotes Therapeutic Resistance

Cell cycle phases (G1, S, G2, M) regulate cell growth, DNA replication, and division in proliferating cells.

Apoptosis regulation involves multiple pathways and molecules for cellular homeostasis.

Questions

1–4 of 4 Questions  
  1. What is Product C9911, (S)-(+)-Camptothecin, soluble in?

    1 answer
    1. This product is soluble in DMSO (10 mg/mL). At higher concentrations, heating is required for the product to dissolve completely (approximately 10 minutes at 95°C), but some precipitation occurs upon cooling to room temperature. It is also soluble in 1 N NaOH (50 mg/mL) and methanol (50 mg/mL).

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  2. What is the Department of Transportation shipping information for this product?

    1 answer
    1. Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product.

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  3. What is the extinction coefficient of Product C9911, (S)-(+)-Camptothecin?

    1 answer
    1. The millimolar extinction coefficients (EmM) at various wavelengths are 37.3 (220 nm); 29.2 (254 nm); 4.9 (290 nm); 19.9 (370 nm).

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  4. What is the solution stability of Product C9911, (S)-(+)-Camptothecin?

    1 answer
    1. Stock solutions of camptothecin in DMSO can be stored at -20°C for up to 3 months.

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