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Valrubicin

HCID 454216
노트반응

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기본 정보이름 및 식별자물성안전 및 규제화학 및 산업관련 반응화합물 노트
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기본 정보

CAS
56124-62-0
표준 SMILES
CCCCC(=O)OCC(=O)[C@]1(O)Cc2c(O)c3c(c(O)c2[C@@H](O[C@H]2C[C@H](NC(=O)C(F)(F)F)[C@H](O)[C@H](C)O2)C1)C(=O)c1c(OC)cccc1C3=O
InChIKey
ZOCKGBMQLCSHFP-KQRAQHLDSA-N
분자식
C34H36F3NO13
평균 분자량
723.65 g/mol
단동위원소 질량
723.21387487

이름 및 식별자

우선 이름
Valrubicin
IUPAC
2-Oxo-2-[(2S,4S)-2,5,12-trihydroxy-7-methoxy-6,11-dioxo-4-{[2,3,6-trideoxy-3-(2,2,2-trifluoroacetamido)-alpha-L-lyxo-hexopyranosyl]oxy}-1,2,3,4,6,11-hexahydrotetracen-2-yl]ethyl pentanoate
영어명
Valrubicin
분자식
C34H36F3NO13
분자량
723.65

이름 및 동의어

ad32CS-703ValstarValtaxinVALRUBICINnsc-246131Aids004409Aids-004409antibioticad32Valrubicin(R&D)

데이터베이스 식별자

CAS
56124-62-0
PubChem CID
454216
DTXSID
DTXSID9046497
ChEMBL
CHEMBL1096885
ChEBI
CHEBI:135876
UNII
2C6NUM6878
EC Number
680-664-1
Nikkaji
J86.660A

물성

물리화학적 성질

녹는점
116 · 116-117 °C
끓는 점
135 · 135-136 C
밀도
1.3473 · 1.3473 (estimate)
저장 조건
2 · 2-8°C
용해도
DMSO(약간 용해됨), 메탄올(약간 용해됨)
물리적 상태
고체
산도 계수 (pKa)
7.34 · 7.34±0.60(Predicted)
색상
빨간색
수용성
불용성
InChIKey
ZOCKGBMQLCSHFP-XGMQQLFPNA-N
SMILES
C12=C(O)C3=C(C(=O)C4C=CC=C(OC)C=4C3=O)C(O)=C1C[C@@](O)(C(=O)COC(=O)CCCC)C[C@@H]2O[C@@H]1O[C@H]([C@@H](O)[C@@H](NC(=O)C(F)(F)F)C1)C |&1:21,34,36,38,39,41,r|

화학적 성질

Red Solid

안전 및 규제

안전 정보는 참고용이며, 공급업체의 물질안전보건자료(SDS), 관련 법규 및 전문가 평가를 대체하지 않습니다.

안전 데이터

독성
dnd-hmn:lym 3 mg/L CJBIAE 58,720,80
HS 번호
2941906000
risk_code
36/37/38
hazard_code
Xi
safety_code
26-37/39
유해 물질 데이터
56124-62-0(Hazardous Substances Data)

화학 및 산업

응용 분야 · 3건

개요Valrubicin was launched as a new 'chemotherapeutic agent for the treatment of bladder cancer, particularly in patients with BCG-refractory carcinoma in situ (CIS) of the bladder for whom immediate cystectomy is unacceptable. It belongs to the class of anthracyclines, the widest used in human cancers, and is a N-trifluoroacetyl 14-valerate derivative of doxorubicin.Valrubicin can be obtained in 3 steps from daunomycin by N-trifluoroacetylation of the sugar moiety then iodination of the 2-acetyl group and introduction of a valerate residue. A proposed mechanism involved in the cytotoxicity of Valrubicin coud be the blockade of SV40 large T antigen helicase; this cellular enzyme is involved in the formation of a ternary complex with DNA to maintain the topographic structure of DNA during transcription. In patients with CIS of bladder refractory to front line and second line therapies, intravesical instillation of Valrubicin resulted in a complete response with a significant rate and allowed a delay in cystectomy. Systemic absorption was minimal and accordingly produced a lower incidence of cardiotoxicity compared with doxorubicin.

용도Valrubicin is a chemotherapy drug used to treat bladder cancer. It is given directly into the bladder as a treatment for carcinoma in situ that does not respond to treatment with bacillus Calmette-Guérin (BCG). It is used in patients who cannot have surgery right away.

일반 설명Valrubicin is available in 200-mg vials for intravesicular administrationin the treatment of bladder cancer (orphan drugstatus). The increased lipophilicity associated with the valericacid ester and trifluoro acetate functionalities increasestissue penetration and remains intact because, in large measure,of the lack of exposure to hydrolyzing enzymes causedby direct delivery into the bladder followed by voiding ofthe instilled solution. This local action also minimizes cardiotoxicityand other adverse effects seen with other anthracyclines.The major adverse effects that are seen are bladderirritation and reddening of the urine.

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