Hu rau:Errol Zhou (Mr.)
Tel: ntxiv 86-551-65523315
Mobile/WhatsApp: ntxiv 86 17705606359
QQ:196299583
Skype:lucytoday@hotmail.com
Email:sales@homesunshinepharma.com
Ntxiv:1002, Huanmao Tsev, No.105, Mengcheng Txoj kev, Hefei Lub zos, 230061 Tuam Tshoj

CAS Nr .: 108212-75-5
Cov roj formula: C55H74IN3O21S4
Molecular Luj: 1368.35000
EINECS NO: 813-745-9
MDL NO: NA
Product Description:
Khoom npe: Calicheamicin CAS NO: 108212-75-5
Synonyms:
calicheamicin gamma 1 (Kuv);
Calichamicin 1I;
Calichamicin Gamma 1;
Chemical Physical Properties:
Cov tsos mob: hmoov
Assay: Ntau dua lossis sib npaug rau 99.0 feem pua
Density: 1.57±0.1 g/cm3(Predicted)
Alpha: D26 -124 degree (c=0.98 feem pua , EtOH)
Pka: 7.13±0.60(Predicted)
The calicheamicins are a class of enediyne antitumor antibiotics derived from the bacterium Micromonospora echinospora, with calicheamicin 1 being the most notable. It was isolated originally in the mid-1980s from the chalky soil, or "calichi pits", located in Kerrville, Texas. The sample was collected by a scientist working for Lederle Labs. It is extremely toxic to all cells and, in 2000, a CD33 antigen-targeted immunoconjugate N-acetyl dimethyl hydrazide calicheamicin was developed and marketed as targeted therapy against the non-solid tumor cancer acute myeloid leukemia (AML). Calicheamicin 1 and the related enediyne esperamicin are the two of the most potent antitumor agents known.
Calicheamicins are a series of enediyne antitumor antibiotics originally isolated from the bacterium Micromonospora echinospora. They exert high cytotoxicity and have been applied in tumor therapies for over a decade-- a CD33 antigen-targeted immuno-conjugate: N-acetyl dimethyl hydrazide calicheamicin, was developed as a targeted therapy for non-solid tumor cancer acute myeloid leukemia (AML). Calicheamicin has several derivatives with different chemical modifications, among which 1 is the most well-characterized. Calicheamicin 1 contains an aglycon consisting of a bicycle tridec-9-ene-2,6-diyne system with a labile methyl trisulfide group and an aryltetrasaccharide chain. Calicheamicins also contain enediyne moieties that are structurally similar to other enediynes, such as esperamicins, neocarzinostatin, and kedarcidin, etc. After reduction by cellular thiols, the calicheamicin enediyne moieties rearrange to produce a 1, 4-benzenoid diradical.
Yog tias koj txaus siab rau peb cov khoom lossis muaj lus nug, thov koj xav tiv tauj peb!
Cov khoom raws li patent yog muab rau RD lub hom phiaj nkaus xwb. Txawm li cas los xij, lub luag haujlwm kawg tsuas yog nrog tus neeg yuav khoom.
Cim npe nrov: Calicheamicin CAS 108212-75-5, tuam ntxhab, lwm tus muag khoom, Hoobkas, yuav, hauv Tshuag