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Cellocidin

Cellocidin structure

Cellocidin 

structure
  • CAS No:

    543-21-5

  • Formula:

    C4H4N2O2

  • Chemical Name:

    Cellocidin

  • Synonyms:

    2-Butynediamide;Acetylenedicarboxamide;Acetylenedicarboxylic acid diamide;Aquamycin;Cellocidin;Lenamycin;Acetylene diamide;NSC 38643;NSC 65381;102489-37-2

  • Categories:

    Chemical Reagents  >  Organic Reagents

Description

CREAM TO BEIGE FINE CRYSTALLINE POWDER


Cellocidin is 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. It has a role as an antimicrobial agent, an antibacterial agent, a metabolite and a pesticide. It is a ynamide, a dicarboxylic acid diamide and a primary carboxamide. It derives from a butynedioic acid.

Cellocidin Basic Attributes

112.09

112.09

200-816-9

1K327HA41T

65381|38643

DTXSID1060261

2924199090

Characteristics

86.2

-1.2

Cream to beige Fine Crystalline Powder

1.41g/cm3

217 °C (decomp)

294ºC at 760 mmHg

131.6ºC

1.56

0.00167mmHg at 25°C

Oral-Mouse LD50: 89.2 mg/kg

Combustion produces toxic nitrogen oxide gas

Safety Information

25-21

45-36/37-28A

T

The warehouse is ventilated, low temperature and dry; stored and transported separately from food materials

P264, P270, P280, P301+P310, P302+P352, P312, P321, P322, P330, P361, P363, P405, P501

H301

|Warning|H302 (95%): Harmful if swallowed [Warning Acute toxicity, oral]|P264, P270, P301+P312, P330, and P501|Aggregated GHS information provided by 40 companies from 3 notifications to the ECHA C&L Inventory.|Danger|H301: Toxic if swallowed [Danger Acute toxicity, oral]|P264, P270, P280, P301+P310, P302+P352, P312, P321, P322, P330, P361, P363, P405, and P501

Toxicity

highly toxic

Drug Information

cellocidin

Cellocidin Use and Manufacturing

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.

2-Butynediamide: INACTIVE

Computed Properties

Molecular Weight:112.09
XLogP3:-1.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Exact Mass:112.027277375
Monoisotopic Mass:112.027277375
Topological Polar Surface Area:86.2
Heavy Atom Count:8
Complexity:165
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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