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ACETYLENEDICARBOXAMIDE

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ACETYLENEDICARBOXAMIDE Basic information

Product Name:
ACETYLENEDICARBOXAMIDE
Synonyms:
  • Acetylendicarbonsaeureamid
  • Acetylenedicarboxylic acid diamide
  • acetylenedicarboxylicaciddiamide
  • Aquamycin
  • Lenamycin
  • Renamycin
  • 2-BUTYNEDIAMIDE
  • ACETYLENEDICARBOXAMIDE
CAS:
543-21-5
MF:
C4H4N2O2
MW:
112.09
EINECS:
684-490-7
Mol File:
543-21-5.mol
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ACETYLENEDICARBOXAMIDE Chemical Properties

Melting point:
179 °C
Boiling point:
209.98°C (rough estimate)
Density 
1.4421 (rough estimate)
refractive index 
1.4610 (estimate)
storage temp. 
Store at -20°C
solubility 
DMF: 10 mg/ml; DMSO: 20 mg/ml; DMSO:PBS (pH 7.2) (1:7): 0.12 mg/ml
form 
Fine Crystalline Powder
pka
13.01±0.50(Predicted)
color 
Cream to beige
EPA Substance Registry System
2-Butynediamide (543-21-5)
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Safety Information

Hazard Codes 
T
Risk Statements 
25-21
Safety Statements 
45-36/37-28A
HS Code 
29241900
Toxicity
LD50 i.v. in mice: 11 mg/kg (Suzuki)

MSDS

  • Language:English Provider:ACROS
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ACETYLENEDICARBOXAMIDE Usage And Synthesis

Description

Cellocidin is an antibiotic originally isolated from S. chibaensis. It is active against various bacterial strains including M. tuberculosis and against the trypanosomes T. brucei and T. rhodesiense (IC50s = 150 and 30 ng/ml, respectively). It inhibits proliferation of LCL1 and LCL2 cells transformed by Epstein-Barr virus (EBV), activates the c-Myc and NF-κB pathways in BC3 and LCL1 cells, and induces necrotic cell death in B cells infected with gammaherpes virus. Cellocidin (100-200 ppm) is protective against bacterial leaf blight in rice plants and inhibits α-ketoglutarate oxidation in X. oryzae, the bacterium that causes leaf blight, when used at a concentration of 1 ppm, suggesting that it inhibits the citric acid cycle. Formulations containing cellocidin have been used as agricultural pesticides.

Chemical Properties

CREAM TO BEIGE FINE CRYSTALLINE POWDER

Uses

Cellocidin is a small neutral alkyne produced by a number of Streptomyces species, first discovered by Suzuki and colleagues in 1958. Cellocidin has a broad antibacterial, antifungal and antitumor profile due to its ability to react with endogenous thiols like cysteine and glutathione. Cellocidin occurs as a weak active in many bioassays using actinomycete crude extracts and is thus a useful standard for chemical and bioassay dereplication.

Definition

ChEBI: A dicarboxylic acid diamide resulting from the formal condensation of both of the carboxy groups of butynedioic acid with ammonia. An antibacterial agent produced by Streptomyces chibaensis.

Purification Methods

Acetylenedicarboxamide crystallises from MeOH and H2O [m 190-192o(dec) as hemihydrate]. When prepared from the ester + NH3 it has m 213o(dec). Also a melting point of 290-292o(dec) has been reported. [Saggimo J Org Chem 22 1171 1857, Kharash et al. J Org Chem 10 392 1945, Blomquist & Winslow J Org Chem 10 156 1945, Beilstein 2 I 317, 2 III 1995, 2 IV 2295.]

ACETYLENEDICARBOXAMIDESupplier

Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006608290; 18621169109
Email
market03@meryer.com
3B Pharmachem (Wuhan) International Co.,Ltd.
Tel
821-50328103-801 18930552037
Email
3bsc@sina.com
Hangzhou Yuhao Chemical Technology Co., Ltd
Tel
0571-82693216
Email
info@yuhaochemical.com
Hangzhou Sage Chemical Co., Ltd.
Tel
+86057186818502 13588463833
Email
info@sagechem.com
Thermo Fisher Scientific
Tel
800-810-5118
Email
cnchemical@thermofisher.com
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