NP-MRD: Showing NP-Card for (2-{2-[(1r,2r,4as)-1,2,5,5-tetramethyl-2,3,4,4a,6,7-hexahydronaphthalen-1-yl]ethyl}-5-(furan-3-yl)pentyl)oxysulfonic acid (NP0224618)

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Record Information

Version

2.0

Created at

2022-09-06 03:05:47 UTC

Updated at

2022-09-06 03:05:47 UTC

NP-MRD ID

NP0224618

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2-{2-[(1r,2r,4as)-1,2,5,5-tetramethyl-2,3,4,4a,6,7-hexahydronaphthalen-1-yl]ethyl}-5-(furan-3-yl)pentyl)oxysulfonic acid

Description

Halisulfate-7 belongs to the class of organic compounds known as sulfuric acid monoesters. These are organic compounds containing the sulfuric acid monoester functional group, with the generic structure ROS(O)(=O)=O, (R=organyl group). (2-{2-[(1r,2r,4as)-1,2,5,5-tetramethyl-2,3,4,4a,6,7-hexahydronaphthalen-1-yl]ethyl}-5-(furan-3-yl)pentyl)oxysulfonic acid is found in Spongia hispida. (2-{2-[(1r,2r,4as)-1,2,5,5-tetramethyl-2,3,4,4a,6,7-hexahydronaphthalen-1-yl]ethyl}-5-(furan-3-yl)pentyl)oxysulfonic acid was first documented in 2007 (PMID: 17979246). Based on a literature review very few articles have been published on halisulfate-7.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062205052D          

 31 33  0  0  1  0            999 V2000
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   -3.4550    0.3447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2795    0.3159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6668   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2296   -1.1121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6169   -1.8406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.2057   -0.0288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5488    0.3817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

 71 73  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1652309062205052D          

 31 33  0  0  1  0            999 V2000
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M  END
> <DATABASE_ID>
NP0224618

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1CC[C@@H]2C(=CCCC2(C)C)[C@]1(C)CCC(CCCC1=COC=C1)COS(O)(=O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C25H40O5S/c1-19-10-11-22-23(9-6-14-24(22,2)3)25(19,4)15-12-20(18-30-31(26,27)28)7-5-8-21-13-16-29-17-21/h9,13,16-17,19-20,22H,5-8,10-12,14-15,18H2,1-4H3,(H,26,27,28)/t19-,20?,22-,25-/m1/s1

> <INCHI_KEY>
OYRXLPLXKXDHJP-MBHHTPPASA-N

> <FORMULA>
C25H40O5S

> <MOLECULAR_WEIGHT>
452.65

> <EXACT_MASS>
452.259645562

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
71

> <JCHEM_AVERAGE_POLARIZABILITY>
51.14414152291266

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(2-{2-[(1R,2R,4aS)-1,2,5,5-tetramethyl-1,2,3,4,4a,5,6,7-octahydronaphthalen-1-yl]ethyl}-5-(furan-3-yl)pentyl)oxy]sulfonic acid

> <JCHEM_LOGP>
5.1711422644613

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
-1.503968608039683

> <JCHEM_PKA_STRONGEST_BASIC>
-2.798841338185813

> <JCHEM_POLAR_SURFACE_AREA>
76.74

> <JCHEM_REFRACTIVITY>
124.15549999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2-{2-[(1R,2R,4aS)-1,2,5,5-tetramethyl-2,3,4,4a,6,7-hexahydronaphthalen-1-yl]ethyl}-5-(furan-3-yl)pentyl)oxysulfonic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      -4.094  -0.609   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.633  -0.663   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -6.449   0.643   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -7.988   0.590   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -8.711  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -7.895  -2.076   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -8.618  -3.436   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0     -10.157  -3.489   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0     -10.973  -2.183   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0     -10.250  -0.824   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0     -11.584  -0.054   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0     -10.358   0.713   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -6.356  -2.022   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -6.249  -3.558   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -5.022  -2.792   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -3.689  -2.022   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.355  -2.792   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.021  -2.022   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.312  -2.792   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.646  -2.022   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.980  -2.792   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.386  -2.166   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.417  -3.310   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       4.647  -4.644   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       3.141  -4.324   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -2.355  -4.332   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -1.021  -5.102   0.000  0.00  0.00           O+0
HETATM   28  S   UNK     0      -1.021  -6.642   0.000  0.00  0.00           S+0
HETATM   29  O   UNK     0      -2.561  -6.642   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       0.519  -6.642   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      -1.021  -8.182   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   13                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   10                                                  
CONECT    6    5    7   13                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    5   11   12                                             
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13    6    2   14   15                                             
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   26                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   25                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   21                                                       
CONECT   26   17   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30   31                                             
CONECT   29   28                                                            
CONECT   30   28                                                            
CONECT   31   28                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   66    0
END

View in JSmol

Synonyms

Value	Source
Halisulfuric acid-7	Generator
Halisulphate-7	Generator
Halisulphuric acid-7	Generator
Halisulfate 7	MeSH

Chemical Formula

C₂₅H₄₀O₅S

Average Mass

452.6500 Da

Monoisotopic Mass

452.25965 Da

IUPAC Name

[(2-{2-[(1R,2R,4aS)-1,2,5,5-tetramethyl-1,2,3,4,4a,5,6,7-octahydronaphthalen-1-yl]ethyl}-5-(furan-3-yl)pentyl)oxy]sulfonic acid

Traditional Name

(2-{2-[(1R,2R,4aS)-1,2,5,5-tetramethyl-2,3,4,4a,6,7-hexahydronaphthalen-1-yl]ethyl}-5-(furan-3-yl)pentyl)oxysulfonic acid

CAS Registry Number

Not Available

SMILES

C[C@@H]1CC[C@@H]2C(=CCCC2(C)C)[C@]1(C)CCC(CCCC1=COC=C1)COS(O)(=O)=O

InChI Identifier

InChI=1S/C25H40O5S/c1-19-10-11-22-23(9-6-14-24(22,2)3)25(19,4)15-12-20(18-30-31(26,27)28)7-5-8-21-13-16-29-17-21/h9,13,16-17,19-20,22H,5-8,10-12,14-15,18H2,1-4H3,(H,26,27,28)/t19-,20?,22-,25-/m1/s1

InChI Key

OYRXLPLXKXDHJP-MBHHTPPASA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Spongia hispida	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sulfuric acid monoesters. These are organic compounds containing the sulfuric acid monoester functional group, with the generic structure ROS(O)(=O)=O, (R=organyl group).

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Organic sulfuric acids and derivatives

Sub Class

Sulfuric acid esters

Direct Parent

Sulfuric acid monoesters

Alternative Parents

Substituents

Alkyl sulfate
Sulfate-ester
Sulfuric acid monoester
Heteroaromatic compound
Furan
Oxacycle
Organoheterocyclic compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	5.17	ChemAxon
pKa (Strongest Acidic)	-1.5	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	76.74 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	124.16 m³·mol⁻¹	ChemAxon
Polarizability	51.14 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

8226150

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10050588

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Carr G, Raszek M, Van Soest R, Matainaho T, Shopik M, Holmes CF, Andersen RJ: Protein phosphatase inhibitors isolated from Spongia irregularis collected in Papua New Guinea. J Nat Prod. 2007 Nov;70(11):1812-5. doi: 10.1021/np0702887. Epub 2007 Nov 3. [PubMed:17979246 ]
LOTUS database [Link]

Showing NP-Card for (2-{2-[(1r,2r,4as)-1,2,5,5-tetramethyl-2,3,4,4a,6,7-hexahydronaphthalen-1-yl]ethyl}-5-(furan-3-yl)pentyl)oxysulfonic acid (NP0224618)

MOL for NP0224618 ((2-{2-[(1r,2r,4as)-1,2,5,5-tetramethyl-2,3,4,4a,6,7-hexahydronaphthalen-1-yl]ethyl}-5-(furan-3-yl)pentyl)oxysulfonic acid)

3D MOL for NP0224618 ((2-{2-[(1r,2r,4as)-1,2,5,5-tetramethyl-2,3,4,4a,6,7-hexahydronaphthalen-1-yl]ethyl}-5-(furan-3-yl)pentyl)oxysulfonic acid)

3D SDF for NP0224618 ((2-{2-[(1r,2r,4as)-1,2,5,5-tetramethyl-2,3,4,4a,6,7-hexahydronaphthalen-1-yl]ethyl}-5-(furan-3-yl)pentyl)oxysulfonic acid)

3D-SDF for NP0224618 ((2-{2-[(1r,2r,4as)-1,2,5,5-tetramethyl-2,3,4,4a,6,7-hexahydronaphthalen-1-yl]ethyl}-5-(furan-3-yl)pentyl)oxysulfonic acid)

PDB for NP0224618 ((2-{2-[(1r,2r,4as)-1,2,5,5-tetramethyl-2,3,4,4a,6,7-hexahydronaphthalen-1-yl]ethyl}-5-(furan-3-yl)pentyl)oxysulfonic acid)

3D PDB for NP0224618 ((2-{2-[(1r,2r,4as)-1,2,5,5-tetramethyl-2,3,4,4a,6,7-hexahydronaphthalen-1-yl]ethyl}-5-(furan-3-yl)pentyl)oxysulfonic acid)

SMILES for NP0224618 ((2-{2-[(1r,2r,4as)-1,2,5,5-tetramethyl-2,3,4,4a,6,7-hexahydronaphthalen-1-yl]ethyl}-5-(furan-3-yl)pentyl)oxysulfonic acid)

INCHI for NP0224618 ((2-{2-[(1r,2r,4as)-1,2,5,5-tetramethyl-2,3,4,4a,6,7-hexahydronaphthalen-1-yl]ethyl}-5-(furan-3-yl)pentyl)oxysulfonic acid)

Structure for NP0224618 ((2-{2-[(1r,2r,4as)-1,2,5,5-tetramethyl-2,3,4,4a,6,7-hexahydronaphthalen-1-yl]ethyl}-5-(furan-3-yl)pentyl)oxysulfonic acid)

3D Structure for NP0224618 ((2-{2-[(1r,2r,4as)-1,2,5,5-tetramethyl-2,3,4,4a,6,7-hexahydronaphthalen-1-yl]ethyl}-5-(furan-3-yl)pentyl)oxysulfonic acid)