NP-MRD: Showing NP-Card for 2,3,7-Triepiaustraline (NP0353539)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2026-02-23 17:46:33 UTC

Updated at

2026-02-23 20:01:13 UTC

NP-MRD ID

NP0353539

Natural Product DOI

https://doi.org/10.57994/8076

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2,3,7-Triepiaustraline

Description

Not Available

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309272007412D          

 14 15  0  0  0  0            999 V2000
   -3.5589    1.0713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0739    0.4040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0739    1.7388    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0197    1.0713    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5046    1.7388    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2893    1.4839    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2893    0.6589    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5046    0.4040    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2497   -0.3806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2893    2.3089    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3288    2.5234    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1947    1.0713    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4428   -0.5521    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2497    2.5234    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  3  1  0  0  0  0
  4  5  1  0  0  0  0
  4  8  1  0  0  0  0
  5  6  1  0  0  0  0
  6  3  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  2  7  1  0  0  0  0
  8  9  1  6  0  0  0
  3 11  1  1  0  0  0
  5 14  1  1  0  0  0
  4 12  1  1  0  0  0
  9 13  1  0  0  0  0
  6 10  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0353539

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@]12[C@H](O)CCN1[C@@H](CO)[C@H](O)[C@@H]2O

> <INCHI_IDENTIFIER>
InChI=1S/C8H15NO4/c10-3-4-7(12)8(13)6-5(11)1-2-9(4)6/h4-8,10-13H,1-3H2/t4-,5+,6+,7-,8+/m0/s1

> <INCHI_KEY>
AIQMLBKBQCVDEY-FMGWEMOISA-N

> <FORMULA>
C8H15NO4

> <MOLECULAR_WEIGHT>
189.211

> <EXACT_MASS>
189.100107967

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
28

> <JCHEM_AVERAGE_POLARIZABILITY>
18.78187492894108

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2S,3S,7R,7aR)-3-(hydroxymethyl)-hexahydro-1H-pyrrolizine-1,2,7-triol

> <ALOGPS_LOGP>
-2.05

> <JCHEM_LOGP>
-2.55449338

> <ALOGPS_LOGS>
0.79

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
14.213749252474837

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.152193183078392

> <JCHEM_PKA_STRONGEST_BASIC>
8.727070358260379

> <JCHEM_POLAR_SURFACE_AREA>
84.16000000000001

> <JCHEM_REFRACTIVITY>
44.4357

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.16e+03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,3S,7R,7aR)-3-(hydroxymethyl)-hexahydro-1H-pyrrolizine-1,2,7-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 27-SEP-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   27-SEP-20         0                                  
HETATM    1  C   UNK     0      -6.643   2.000   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.738   0.754   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.738   3.246   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.903   2.000   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.809   3.246   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -4.273   2.770   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0      -4.273   1.230   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0      -2.809   0.754   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.333  -0.710   0.000  0.00  0.00           C+0
HETATM   10  H   UNK     0      -4.273   4.310   0.000  0.00  0.00           H+0
HETATM   11  O   UNK     0      -6.214   4.710   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0      -0.363   2.000   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0      -0.827  -1.031   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0      -2.333   4.710   0.000  0.00  0.00           O+0
CONECT    1    2    3                                                       
CONECT    2    1    7                                                       
CONECT    3    1    6   11                                                  
CONECT    4    5    8   12                                                  
CONECT    5    4    6   14                                                  
CONECT    6    5    3    7   10                                             
CONECT    7    6    8    2                                                  
CONECT    8    4    7    9                                                  
CONECT    9    8   13                                                       
CONECT   10    6                                                            
CONECT   11    3                                                            
CONECT   12    4                                                            
CONECT   13    9                                                            
CONECT   14    5                                                            
MASTER        0    0    0    0    0    0    0    0   14    0   30    0
END

View in JSmol

Synonyms

Value	Source
(-)-1-epi-Alexine	PhytoBank
2,3,7-Triepi-australine	PhytoBank

Chemical Formula

C₈H₁₅NO₄

Average Mass

189.2110 Da

Monoisotopic Mass

189.10011 Da

IUPAC Name

(1R,2S,3S,7R,7aR)-3-(hydroxymethyl)-hexahydro-1H-pyrrolizine-1,2,7-triol

Traditional Name

(1R,2S,3S,7R,7aR)-3-(hydroxymethyl)-hexahydro-1H-pyrrolizine-1,2,7-triol

CAS Registry Number

Not Available

SMILES

[H][C@]12[C@H](O)CCN1[C@@H](CO)[C@H](O)[C@@H]2O

InChI Identifier

InChI=1S/C8H15NO4/c10-3-4-7(12)8(13)6-5(11)1-2-9(4)6/h4-8,10-13H,1-3H2/t4-,5+,6+,7-,8+/m0/s1

InChI Key

AIQMLBKBQCVDEY-FMGWEMOISA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View

Predicted Spectra

Not Available

Chemical Shift Submissions

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹H NMR Spectrum (1D, 400.0, D₂O, simulated)	[email protected]	Not Available	Not Available	2026-02-23	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100.0, D₂O, simulated)	[email protected]	Not Available	Not Available	2026-02-23	View Spectrum

Species

Species of Origin

Species Name	Source	Reference
Castanospermum australe		Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyrrolizidines. Pyrrolizidines are compounds containing a pyrrolizidine, which is a bicyclic ring system made up of two fused pyrrolidine ring sharing a nitrogen atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pyrrolizidines

Sub Class

Not Available

Direct Parent

Pyrrolizidines

Alternative Parents

Substituents

Pyrrolizidine
N-alkylpyrrolidine
Pyrrolidine
Secondary alcohol
Tertiary amine
Tertiary aliphatic amine
1,2-aminoalcohol
Polyol
Azacycle
Alcohol
Organic oxygen compound
Organic nitrogen compound
Organopnictogen compound
Primary alcohol
Organooxygen compound
Organonitrogen compound
Amine
Hydrocarbon derivative
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	-2	ALOGPS
logP	-2.6	ChemAxon
logS	0.79	ALOGPS
pKa (Strongest Acidic)	13.15	ChemAxon
pKa (Strongest Basic)	8.73	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	84.16 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	44.44 m³·mol⁻¹	ChemAxon
Polarizability	18.78 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB031384

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

21576628

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

DOI: 10.1016/s0957-4166(02)00799-1

Showing NP-Card for 2,3,7-Triepiaustraline (NP0353539)

MOL for NP0353539 (2,3,7-Triepiaustraline)

3D MOL for NP0353539 (2,3,7-Triepiaustraline)

3D SDF for NP0353539 (2,3,7-Triepiaustraline)

3D-SDF for NP0353539 (2,3,7-Triepiaustraline)

PDB for NP0353539 (2,3,7-Triepiaustraline)

3D PDB for NP0353539 (2,3,7-Triepiaustraline)

SMILES for NP0353539 (2,3,7-Triepiaustraline)

INCHI for NP0353539 (2,3,7-Triepiaustraline)

Structure for NP0353539 (2,3,7-Triepiaustraline)

3D Structure for NP0353539 (2,3,7-Triepiaustraline)