ChemSpider 2D Image | Romidepsin | C24H36N4O6S2

Romidepsin

  • Molecular FormulaC24H36N4O6S2
  • Average mass540.696 Da
  • Monoisotopic mass540.207642 Da
  • ChemSpider ID10122002
  • Double-bond stereo - Double-bond stereo

    defined stereocentres - 4 of 4 defined stereocentres


More details:



Featured data source



Validated by Experts, Validated by Users, Non-Validated, Removed by Users

(1S,4S,7Z,10S,21R)-7-Ethyliden-4,21-diisopropyl-2-oxa-12,13-dithia-5,8,20,23-tetraazabicyclo[8.7.6]tricos-16-en-3,6,9,19,22-penton [German] [ACD/IUPAC Name]
(1S,4S,7Z,10S,21R)-7-ethylidene-4,21-di(propan-2-yl)-2-oxa-12,13-dithia-5,8,20,23-tetraazabicyclo[8.7.6]tricos-16-ene-3,6,9,19,22-pentone
(1S,4S,7Z,10S,21R)-7-Ethylidene-4,21-diisopropyl-2-oxa-12,13-dithia-5,8,20,23-tetraazabicyclo[8.7.6]tricos-16-ene-3,6,9,19,22-pentone [ACD/IUPAC Name]
(1S,4S,7Z,10S,21R)-7-Éthylidène-4,21-diisopropyl-2-oxa-12,13-dithia-5,8,20,23-tétraazabicyclo[8.7.6]tricos-16-ène-3,6,9,19,22-pentone [French] [ACD/IUPAC Name]
128517-07-7 [RN]
2-Oxa-12,13-dithia-5,8,20,23-tetraazabicyclo[8.7.6]tricos-16-ene-3,6,9,19,22-pentone, 7-ethylidene-4,21-bis(1-methylethyl)-, (1S,4S,7Z,10S,21R)- [ACD/Index Name]
8656
CX3T89XQBK
romidepsina [Spanish] [INN]
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Validated by Experts, Validated by Users, Non-Validated, Removed by Users

FK 228 [DBID]
FK228 [DBID]
FK-228 [DBID]
FR 901228 [DBID]
FR901228 [DBID]
FR-901228 [DBID]
NSC 630176 [DBID]
NSC-630176 [DBID]
  • Experimental Physico-chemical Properties
  • Miscellaneous
    • Chemical Class:

      A cyclodepsipeptide consisting of the cyclic disulfide of (2<stereo>Z</stereo>)-2-aminobut-2-enoyl, <stereo>L</stereo>-valyl, (3<stereo>S</stereo>,4<stereo>E</stereo>)-3-hydroxy-7-sulfanylhept-4-enoyl , <stereo>D</stereo>-valyl and <stereo>D</stereo>-cysteinyl residues coupled in sequence and cyclised head-to tail. ChEBI CHEBI:61080
    • Bio Activity:

      Deacetylases Tocris Bioscience 3515
      Enzymes Tocris Bioscience 3515
      Histone Deacetylases Tocris Bioscience 3515
      Potent and selective class I histone deacetylase inhibitor; antitumor Tocris Bioscience 3515
      Potent and selective inhibitor of class I histone deacetylases (HDACs) (IC50 values are 36, 47, 510 and 14,000 nM for HDAC1, HDAC2, HDAC4 and HDAC6 respectively). Exhibits cytotoxicity against various human tumor cell lines; also exhibits antitumor activity against human tumor xenografts. Tocris Bioscience 3515

Predicted data is generated using the ACD/Labs Percepta Platform - PhysChem Module

Density: 1.2±0.1 g/cm3
Boiling Point: 942.8±65.0 °C at 760 mmHg
Vapour Pressure: 0.0±0.3 mmHg at 25°C
Enthalpy of Vaporization: 137.3±3.0 kJ/mol
Flash Point: 524.0±34.3 °C
Index of Refraction: 1.529
Molar Refractivity: 142.0±0.3 cm3
#H bond acceptors: 10
#H bond donors: 4
#Freely Rotating Bonds: 2
#Rule of 5 Violations: 2
ACD/LogP: 0.95
ACD/LogD (pH 5.5): 1.04
ACD/BCF (pH 5.5): 3.65
ACD/KOC (pH 5.5): 88.00
ACD/LogD (pH 7.4): 1.04
ACD/BCF (pH 7.4): 3.65
ACD/KOC (pH 7.4): 87.99
Polar Surface Area: 193 Å2
Polarizability: 56.3±0.5 10-24cm3
Surface Tension: 39.7±3.0 dyne/cm
Molar Volume: 460.4±3.0 cm3

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