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MFCD09971005 molecular structure
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[(1R,2R,6R,11R,13S,15R,17R)-13-benzyl-6-hydroxy-4,17-dimethyl-5-oxo-15-(prop-1-en-2-yl)-12,14,18-trioxapentacyclo[11.4.1.01,10.02,6.011,15]octadeca-3,8-dien-8-yl]methyl 2-(4-hydroxy-2-iodo-5-methoxyphenyl)acetate

ChemBase ID: 154238
Molecular Formular: C37H39IO9
Molecular Mass: 754.60463
Monoisotopic Mass: 754.16388083
SMILES and InChIs

SMILES:
C[C@@H]1C[C@]2([C@H]3C4[C@]1([C@@H]1C=C(C(=O)[C@]1(CC(=C4)COC(=O)Cc1cc(c(cc1I)O)OC)O)C)O[C@](O3)(O2)Cc1ccccc1)C(=C)C
Canonical SMILES:
COc1cc(CC(=O)OCC2=CC3[C@H]4O[C@]5(O[C@]3([C@H]3[C@@](C2)(O)C(=O)C(=C3)C)[C@@H](C[C@@]4(O5)C(=C)C)C)Cc2ccccc2)c(cc1O)I
InChI:
InChI=1S/C37H39IO9/c1-20(2)35-16-22(4)37-26(33(35)45-36(46-35,47-37)18-23-9-7-6-8-10-23)12-24(17-34(42)30(37)11-21(3)32(34)41)19-44-31(40)14-25-13-29(43-5)28(39)15-27(25)38/h6-13,15,22,26,30,33,39,42H,1,14,16-19H2,2-5H3/t22-,26?,30-,33-,34-,35-,36-,37-/m1/s1
InChIKey:
IITCVPTZKLXSKQ-DCLOTLOASA-N

Cite this record

CBID:154238 http://www.chembase.cn/molecule-154238.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
[(1R,2R,6R,11R,13S,15R,17R)-13-benzyl-6-hydroxy-4,17-dimethyl-5-oxo-15-(prop-1-en-2-yl)-12,14,18-trioxapentacyclo[11.4.1.01,10.02,6.011,15]octadeca-3,8-dien-8-yl]methyl 2-(4-hydroxy-2-iodo-5-methoxyphenyl)acetate
IUPAC Traditional name
[(1R,2R,6R,11R,13S,15R,17R)-13-benzyl-6-hydroxy-4,17-dimethyl-5-oxo-15-(prop-1-en-2-yl)-12,14,18-trioxapentacyclo[11.4.1.01,10.02,6.011,15]octadeca-3,8-dien-8-yl]methyl 2-(4-hydroxy-2-iodo-5-methoxyphenyl)acetate
Synonyms
6-I-RTX
Resiniferonyl 20-(4-hydroxy-2-iodo-5-methoxyphenylacetate 9,13,14-ortho(phenylacetate)
6′-Iodoresiniferatoxin
MDL Number
MFCD09971005
PubChem SID
162248377
PubChem CID
71311820

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID Price
Sigma Aldrich
I7033 external link Add to cart Please log in.
Data Source Data ID
PubChem 71311820 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 9.284033  H Acceptors
H Donor LogD (pH = 5.5) 6.5177464 
LogD (pH = 7.4) 6.5122213  Log P 6.5178175 
Molar Refractivity 183.4675 cm3 Polarizability 71.448395 Å3
Polar Surface Area 120.75 Å2 Rotatable Bonds
Lipinski's Rule of Five false 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Apperance
colorless or white amorphous semi-solid expand Show data source
MSDS Link
Download expand Show data source
German water hazard class
3 expand Show data source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter expand Show data source
Storage Temperature
-20°C expand Show data source
Empirical Formula (Hill Notation)
C37H39O9I expand Show data source

DETAILS

DETAILS

Sigma Aldrich Sigma Aldrich
Sigma Aldrich - I7033 external link
Biochem/physiol Actions
VR1 vanilloid receptor partial agonist.

REFERENCES

REFERENCES

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PATENTS

PATENTS

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INTERNET

INTERNET

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