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Merck
모든 사진(1)

주요 문서

C9705

Sigma-Aldrich

Concanamycin A

≥70% (HPLC), crystals, vacuolar-type v-ATPase inhibitor

동의어(들):

Folimycin

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크기 선택

25 μG
₩380,727
0.1 MG
₩1,123,605

₩380,727


출고 가능일2025년 4월 09일세부사항


벌크 견적 요청

크기 선택

보기 변경
25 μG
₩380,727
0.1 MG
₩1,123,605

About This Item

실험식(Hill 표기법):
C46H75NO14
CAS Number:
Molecular Weight:
866.09
Beilstein:
3560277
MDL number:
UNSPSC 코드:
12352200
PubChem Substance ID:
NACRES:
NA.77

₩380,727


출고 가능일2025년 4월 09일세부사항


벌크 견적 요청

제품명

Concanamycin A, ≥70% (HPLC)

Quality Level

분석

≥70% (HPLC)

양식

solid film

항생제 활성 스펙트럼

viruses

동작 모드

enzyme | inhibits

저장 온도

−20°C

SMILES string

CCC1C(O)C(C)C\C(C)=C\C=C\C(OC)C(OC(=O)\C(OC)=C\C(C)=C\C(C)C1O)C(C)C(O)C(C)[C@]2(O)C[C@@H](O[C@H]3C[C@@H](O)[C@H](OC(N)=O)[C@@H](C)O3)[C@H](C)C(O2)\C=C\C

InChI

1S/C46H75NO14/c1-13-16-34-28(7)37(58-38-22-33(48)43(31(10)57-38)60-45(47)53)23-46(54,61-34)30(9)41(51)29(8)42-35(55-11)18-15-17-24(3)19-26(5)39(49)32(14-2)40(50)27(6)20-25(4)21-36(56-12)44(52)59-42/h13,15-18,20-21,26-35,37-43,48-51,54H,14,19,22-23H2,1-12H3,(H2,47,53)/b16-13+,18-15+,24-17+,25-20+,36-21-/t26?,27?,28-,29?,30?,31-,32?,33-,34?,35?,37-,38+,39?,40?,41?,42?,43-,46+/m1/s1

InChI key

DJZCTUVALDDONK-LWLXYWDNSA-N

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일반 설명

Chemical structure: macrolide
Concanamycin A belongs to the plecomacrolide family[1] and comprises an 18-membered tetraenic macrolide ring.[2]

애플리케이션

Concanamycin A has been used:
  • as a lysosomal inhibitor in young and old fibroblasts[3]
  • as a vacuolar-type H+-ATPase inhibitor in presynaptic vesicles[4]
  • as a lysosomal acidification blocker in HepG2 hepatocytes cells[5]

생화학적/생리학적 작용

Concanamycin A (ConA) inhibits acidification of organelles[1] and perforin-mediated cytotoxicity.[6] It is a vacuolar-type v-ATPase inhibitor.[7] ConA possesses antiprotozoal and antineoplastic properties.[2] It mediates inhibition of the negative factor (Nef) protein of the human immunodeficiency virus.[1]

픽토그램

Skull and crossbones

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 1 Inhalation - Acute Tox. 2 Dermal - Acute Tox. 2 Oral - Eye Irrit. 2

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

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


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문서 라이브러리 방문

Hideaki Toda et al.
Developmental and comparative immunology, 35(1), 88-93 (2010-09-04)
T cell-mediated cytotoxicity occurs via pathways based on perforin or Fas mechanisms. Perforin is a protein present in the cytoplasmic granules of CD8(+) cytotoxic T lymphocytes and is secreted to form pores on target cell membranes. In fish, although the
Stephen F Haydock et al.
Microbiology (Reading, England), 151(Pt 10), 3161-3169 (2005-10-07)
The macrolide antibiotic concanamycin A has been identified as an exceptionally potent inhibitor of the vacuolar (V-type) ATPase. Such compounds have been mooted as the basis of a potential drug treatment for osteoporosis, since the V-ATPase is involved in the
Christiane Ott et al.
Redox biology, 10, 266-273 (2016-11-09)
The overall decrease in proteolytic activity in aging can promote and accelerate protein accumulation and metabolic disturbances. To specifically analyze changes in macroautophagy (MA) we quantified different autophagy-related proteins (ATGs) in young, adult and old murine tissue as well as
Mark M Painter et al.
Proceedings of the National Academy of Sciences of the United States of America, 117(38), 23835-23846 (2020-09-10)
Nef is an HIV-encoded accessory protein that enhances pathogenicity by down-regulating major histocompatibility class I (MHC-I) expression to evade killing by cytotoxic T lymphocytes (CTLs). A potent Nef inhibitor that restores MHC-I is needed to promote immune-mediated clearance of HIV-infected
Jörn Dengjel et al.
Molecular & cellular proteomics : MCP, 11(3), M111-M111 (2012-02-09)
Autophagy is one of the major intracellular catabolic pathways, but little is known about the composition of autophagosomes. To study the associated proteins, we isolated autophagosomes from human breast cancer cells using two different biochemical methods and three stimulus types:

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