Home > Compound List > Compound details
53760-20-6 molecular structure
click picture or here to close

(3S,4S,6S,6aR,10S,12S,15R,15aR,15bR)-3-benzyl-6,12,15-trihydroxy-4,10,12-trimethyl-5-methylidene-1H,2H,3H,4H,5H,6H,6aH,9H,10H,11H,12H,15H,15bH-cycloundeca[e]isoindol-1-one

ChemBase ID: 156667
Molecular Formular: C28H37NO4
Molecular Mass: 451.59768
Monoisotopic Mass: 451.27225867
SMILES and InChIs

SMILES:
C[C@@H]1CC=C[C@@H]2[C@@H](C(=C)[C@H]([C@@H]3[C@@]2([C@@H](C=C[C@@](C1)(C)O)O)C(=O)N[C@H]3Cc1ccccc1)C)O
Canonical SMILES:
C[C@@H]1CC=C[C@@H]2[C@H](O)C(=C)[C@H]([C@@H]3[C@@]2([C@@H](C=C[C@@](C1)(C)O)O)C(=O)N[C@H]3Cc1ccccc1)C
InChI:
InChI=1S/C28H37NO4/c1-17-9-8-12-21-25(31)19(3)18(2)24-22(15-20-10-6-5-7-11-20)29-26(32)28(21,24)23(30)13-14-27(4,33)16-17/h5-8,10-14,17-18,21-25,30-31,33H,3,9,15-16H2,1-2,4H3,(H,29,32)/t17-,18+,21-,22-,23+,24-,25+,27+,28+/m0/s1
InChIKey:
UKQNIEMKORIOQM-HFZGEGEASA-N

Cite this record

CBID:156667 http://www.chembase.cn/molecule-156667.html

Collapse All Expand All

NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
(3S,4S,6S,6aR,10S,12S,15R,15aR,15bR)-3-benzyl-6,12,15-trihydroxy-4,10,12-trimethyl-5-methylidene-1H,2H,3H,4H,5H,6H,6aH,9H,10H,11H,12H,15H,15bH-cycloundeca[e]isoindol-1-one
IUPAC Traditional name
(3S,4S,6S,6aR,10S,12S,15R,15aR,15bR)-3-benzyl-6,12,15-trihydroxy-4,10,12-trimethyl-5-methylidene-2H,3H,4H,6H,6aH,9H,10H,11H,15H,15bH-cycloundeca[e]isoindol-1-one
Synonyms
Cytochalasin J from Phomopsis sp.
CAS Number
53760-20-6
MDL Number
MFCD00077708
PubChem SID
162250804
PubChem CID
71312347

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID Price
Sigma Aldrich
30394 external link Add to cart Please log in.
Data Source Data ID
PubChem 71312347 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 13.708873  H Acceptors
H Donor LogD (pH = 5.5) 2.929523 
LogD (pH = 7.4) 2.9295235  Log P 2.9295237 
Molar Refractivity 131.8062 cm3 Polarizability 51.00005 Å3
Polar Surface Area 89.79 Å2 Rotatable Bonds
Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Safety Information Product Information Bioassay(PubChem)
European Hazard Symbols
Highly toxic Highly toxic (T+) expand Show data source
UN Number
2811 expand Show data source
MSDS Link
Download expand Show data source
German water hazard class
3 expand Show data source
Hazard Class
6.1 expand Show data source
Packing Group
2 expand Show data source
Risk Statements
26/27/28-40 expand Show data source
Safety Statements
22-36/37/39-45 expand Show data source
GHS Pictograms
GHS06 expand Show data source
GHS08 expand Show data source
GHS Signal Word
Danger expand Show data source
GHS Hazard statements
H300-H310-H330-H351 expand Show data source
GHS Precautionary statements
P260-P264-P280-P284-P302 + P350-P310 expand Show data source
Personal Protective Equipment
Eyeshields, Faceshields, full-face particle respirator type N100 (US), Gloves, respirator cartridge type N100 (US), type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges expand Show data source
RID/ADR
UN 2811 6.1/PG 2 expand Show data source
Storage Temperature
-20°C expand Show data source
Purity
≥99.0% (TLC) expand Show data source
Empirical Formula (Hill Notation)
C28H37NO4 expand Show data source

DETAILS

DETAILS

Sigma Aldrich Sigma Aldrich
Sigma Aldrich - 30394 external link
Biochem/physiol Actions
Arrests the cell cycle when applied in prophase or proanaphase. Microtubules at the centrosome are fragmented, and fewer microtubules insert into the kinetochore.1

REFERENCES

REFERENCES

From Suppliers Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
    No data available
  • Searching...Please wait...

PATENTS

PATENTS

PubChem iconPubChem Patent Google Patent Search IconGoogle Patent

INTERNET

INTERNET

Baidu iconBaidu google iconGoogle