NP-MRD: Showing NP-Card for trans-Nerolidol (NP0137525)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-05-30 16:55:04 UTC

Updated at

2022-05-30 16:55:04 UTC

NP-MRD ID

NP0137525

Secondary Accession Numbers

None

Natural Product Identification

Common Name

trans-Nerolidol

Description

Nerolidol belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. trans-Nerolidol is found in Achillea millefolium, Achillea nobilis, Aframomum angustifolium, Ageratum conyzoides, Alpinia chinensis, Aristolochia elegans, Aster scaber, Atalantia buxifolia, Baccharis articulata, Baccharis sessiliflora, Baccharis uncinella, Cananga odorata, Canella winterana, Chrysanthemum indicum, Citrus aurantium, Comptonia peregrina, Croton cajucara, Elsholtzia blanda, Hamamelis virginiana, Hedychium coronarium, Hedychium spicatum, Helichrysum italicum, Helichrysum stoechas, Hexalobus crispiflorus, Kunzea salina, Lantana camara, Lavandula angustifolia, Lentinellus cochleatus, Lepechinia floribunda, Matricaria chamomilla, Melaleuca quinquenervia, Micromeria biflora, Micromeria varia, Morina persica, Origanum cordifolium, Origanum vulgare, Paeonia lactiflora, Pelargonium endlicherianum, Persea americana, Piper auritum, Piper cernuum, Piper regnellii, Piper vitaceum, Pittosporum balfourii, Platostoma africanum, Plumeria obtusa, Populus alba, Rhododendron calostrotum, Salvia dorisiana, Santalum spicatum, Solidago canadensis, Tagetes lucida, Teucrium cyprium, Thulinella chrysantha, Tordylium apulum, Virola surinamensis, Zingiber officinale and Zingiber zerumbet. Nerolidol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 42 41  0  0  0  0  0  0  0  0999 V2000
    5.3092    0.8437   -1.2632 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6602   -0.2337   -0.8568 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0251   -0.1663    0.5143 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4483    1.1965    0.6437 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1392   -0.2217    1.3918 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1290   -1.3150    0.7656 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9342   -1.4839   -0.0954 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9453   -0.3971   -0.0863 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3284   -0.5925    0.3413 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6960   -1.9548    0.8051 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3323    0.5087    0.3512 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4740    0.0631   -0.5558 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4747    1.1551   -0.5489 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6931    0.9115   -0.1276 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0847   -0.4482    0.3441 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7141    2.0120   -0.1171 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7993    0.8858   -2.2396 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4009    1.7487   -0.6675 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6055   -1.0899   -1.4867 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2293    1.6227   -0.3509 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1666    1.9035    1.1428 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5892    1.1716    1.3275 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7983    0.0860    2.2774 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7404   -1.2214    1.8290 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7787   -2.2451    0.7600 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3945   -2.4059    0.2875 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1992   -1.7822   -1.1462 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1078    0.6224   -0.4140 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0582   -2.1779    1.6987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6002   -2.7202    0.0109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7391   -1.9623    1.1888 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8941    1.4608    0.0018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6849    0.6668    1.3776 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1095   -0.0336   -1.5989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8681   -0.8876   -0.1743 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1733    2.1313   -0.8936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4030   -0.8069    1.1671 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1139   -0.4109    0.7827 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0350   -1.1529   -0.5260 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6951    1.5274   -0.3176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4807    2.7706   -0.8907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7477    2.4216    0.9073 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  7  1  0
  7  6  1  0
  6  3  1  0
  3  4  1  0
  3  5  1  1
  3  2  1  0
  2  1  2  3
  8  9  2  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  3
 14 15  1  0
 14 16  1  0
  8 28  1  0
  7 26  1  0
  7 27  1  0
  6 24  1  0
  6 25  1  0
  4 20  1  0
  4 21  1  0
  4 22  1  0
  5 23  1  0
  2 19  1  0
  1 17  1  0
  1 18  1  0
 10 29  1  0
 10 30  1  0
 10 31  1  0
 11 32  1  0
 11 33  1  0
 12 34  1  0
 12 35  1  0
 13 36  1  0
 15 37  1  0
 15 38  1  0
 15 39  1  0
 16 40  1  0
 16 41  1  0
 16 42  1  0
M  END


  Mrv1572004161622512D          

 17 16  0  0  0  0            999 V2000
    3.7125    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8875   -2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8875   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1895    1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2375   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500   -1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4750   -1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7605    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375   -0.7145    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  1  2  0  0  0  0
  9  7  1  0  0  0  0
 10  7  1  0  0  0  0
 11  8  1  0  0  0  0
 12  8  1  0  0  0  0
 13  2  1  0  0  0  0
 13  3  1  0  0  0  0
 13  9  2  0  0  0  0
 14  4  1  0  0  0  0
 14 10  1  0  0  0  0
 14 11  2  0  0  0  0
 15  5  1  0  0  0  0
 15  6  1  0  0  0  0
 15 12  1  0  0  0  0
 16 15  1  0  0  0  0
 17 11  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0137525

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]\C(CCC(C)(O)C=C)=C(\C)CCC=C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C15H26O/c1-6-15(5,16)12-8-11-14(4)10-7-9-13(2)3/h6,9,11,16H,1,7-8,10,12H2,2-5H3/b14-11+

> <INCHI_KEY>
FQTLCLSUCSAZDY-SDNWHVSQSA-N

> <FORMULA>
C15H26O

> <MOLECULAR_WEIGHT>
222.372

> <EXACT_MASS>
222.198365457

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
28.721938535450253

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(6E)-3,7,11-trimethyldodeca-1,6,10-trien-3-ol

> <ALOGPS_LOGP>
4.55

> <JCHEM_LOGP>
4.307206727666666

> <ALOGPS_LOGS>
-4.02

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.459388332120984

> <JCHEM_PKA_STRONGEST_BASIC>
-1.2856635435302817

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
74.00919999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.12e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
nerolidol

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 16-APR-16   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-16         0                                  
HETATM    1  C   UNK     0       6.930   4.001   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.390  -4.001   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.390  -1.334   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.770   1.334   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.954   1.897   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.390   4.001   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.310  -1.334   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.310   1.334   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -3.080  -2.667   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.770  -1.334   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.540   0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.850   1.334   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -4.620  -2.667   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.620   2.667   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       3.286   3.437   0.000  0.00  0.00           O+0
HETATM   17  H   UNK     0       2.310  -1.334   0.000  0.00  0.00           H+0
CONECT    1    6                                                            
CONECT    2   13                                                            
CONECT    3   13                                                            
CONECT    4   14                                                            
CONECT    5   15                                                            
CONECT    6    1   15                                                       
CONECT    7    9   10                                                       
CONECT    8   11   12                                                       
CONECT    9    7   13                                                       
CONECT   10    7   14                                                       
CONECT   11    8   14   17                                                  
CONECT   12    8   15                                                       
CONECT   13    2    3    9                                                  
CONECT   14    4   10   11                                                  
CONECT   15    5    6   12   16                                             
CONECT   16   15                                                            
CONECT   17   11                                                            
MASTER        0    0    0    0    0    0    0    0   17    0   32    0
END

View in JSmol

Synonyms

Value	Source
trans-Nerolidol	ChEMBL
Nerolidol, (S-(e))-isomer	MeSH
Nerolidol, (Z)-isomer	MeSH
Nerolidol, (e)-isomer	MeSH
Nerolidol, (S-(Z))-isomer	MeSH
Peruviol	MeSH
Nerolidol	MeSH
3,7,11-Trimethyl-1,6,10-dodecatrien-3-ol	MeSH

Chemical Formula

C₁₅H₂₆O

Average Mass

222.3720 Da

Monoisotopic Mass

222.19837 Da

IUPAC Name

(6E)-3,7,11-trimethyldodeca-1,6,10-trien-3-ol

Traditional Name

nerolidol

CAS Registry Number

Not Available

SMILES

[H]\C(CCC(C)(O)C=C)=C(\C)CCC=C(C)C

InChI Identifier

InChI=1S/C15H26O/c1-6-15(5,16)12-8-11-14(4)10-7-9-13(2)3/h6,9,11,16H,1,7-8,10,12H2,2-5H3/b14-11+

InChI Key

FQTLCLSUCSAZDY-SDNWHVSQSA-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
Achillea millefolium	LOTUS Database	35616633
Achillea nobilis	LOTUS Database	35616633
Aframomum angustifolium	LOTUS Database	35616633
Ageratum conyzoides	LOTUS Database	35616633
Alpinia chinensis	LOTUS Database	35616633
Aristolochia elegans	LOTUS Database	35616633
Aster scaber	LOTUS Database	35616633
Atalantia buxifolia	LOTUS Database	35616633
Baccharis articulata	LOTUS Database	35616633
Baccharis sessiliflora	LOTUS Database	35616633
Baccharis uncinella	LOTUS Database	35616633
Cananga odorata	LOTUS Database	35616633
Canella winterana	LOTUS Database	35616633
Chrysanthemum indicum	LOTUS Database	35616633
Citrus aurantium	LOTUS Database	35616633
Comptonia peregrina	LOTUS Database	35616633
Croton cajucara	LOTUS Database	35616633
Elsholtzia blanda	LOTUS Database	35616633
Hamamelis virginiana	LOTUS Database	35616633
Hedychium coronarium	LOTUS Database	35616633
Hedychium spicatum	LOTUS Database	35616633
Helichrysum italicum	LOTUS Database	35616633
Helichrysum stoechas	LOTUS Database	35616633
Hexalobus crispiflorus	LOTUS Database	35616633
Kunzea salina	LOTUS Database	35616633
Lantana camara	LOTUS Database	35616633
Lavandula angustifolia	LOTUS Database	35616633
Lentinellus cochleatus	LOTUS Database	35616633
Lepechinia floribunda	LOTUS Database	35616633
Matricaria chamomilla	LOTUS Database	35616633
Melaleuca quinquenervia	LOTUS Database	35616633
Micromeria biflora	LOTUS Database	35616633
Micromeria varia	LOTUS Database	35616633
Morina persica	LOTUS Database	35616633
Origanum cordifolium	LOTUS Database	35616633
Origanum vulgare	LOTUS Database	35616633
Paeonia lactiflora	LOTUS Database	35616633
Pelargonium endlicherianum	LOTUS Database	35616633
Persea americana	LOTUS Database	35616633
Piper auritum	LOTUS Database	35616633
Piper cernuum	LOTUS Database	35616633
Piper regnellii	LOTUS Database	35616633
Piper vitaceum	LOTUS Database	35616633
Pittosporum balfourii	LOTUS Database	35616633
Platostoma africanum	LOTUS Database	35616633
Plumeria obtusa	LOTUS Database	35616633
Populus alba	LOTUS Database	35616633
Rhododendron calostrotum	LOTUS Database	35616633
Salvia dorisiana	LOTUS Database	35616633
Santalum spicatum	LOTUS Database	35616633
Solidago canadensis	LOTUS Database	35616633
Tagetes lucida	LOTUS Database	35616633
Teucrium cyprium	LOTUS Database	35616633
Thulinella chrysantha	LOTUS Database	35616633
Tordylium apulum	LOTUS Database	35616633
Virola surinamensis	LOTUS Database	35616633
Zingiber officinale	LOTUS Database	35616633
Zingiber zerumbet	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Farsesane sesquiterpenoid
Sesquiterpenoid
Tertiary alcohol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic 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	4.55	ALOGPS
logP	4.31	ChemAxon
logS	-4	ALOGPS
pKa (Strongest Acidic)	18.46	ChemAxon
pKa (Strongest Basic)	-1.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	20.23 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	74.01 m³·mol⁻¹	ChemAxon
Polarizability	28.72 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Nerolidol

METLIN ID

Not Available

PubChem Compound

5284507

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for trans-Nerolidol (NP0137525)

MOL for NP0137525 (trans-Nerolidol)

3D MOL for NP0137525 (trans-Nerolidol)

3D SDF for NP0137525 (trans-Nerolidol)

3D-SDF for NP0137525 (trans-Nerolidol)

PDB for NP0137525 (trans-Nerolidol)

3D PDB for NP0137525 (trans-Nerolidol)

SMILES for NP0137525 (trans-Nerolidol)

INCHI for NP0137525 (trans-Nerolidol)

Structure for NP0137525 (trans-Nerolidol)

3D Structure for NP0137525 (trans-Nerolidol)