NP-MRD: Showing NP-Card for (+)-Angustanoic acid C (NP0082993)

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Record Information

Version

2.0

Created at

2022-04-29 04:03:15 UTC

Updated at

2022-04-29 04:03:15 UTC

NP-MRD ID

NP0082993

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Angustanoic acid C

Description

Angustanoic acid C, also known as angustanoate C, belongs to the class of organic compounds known as 1,2-dioxanes. These are organic compounds containing 1,2-dioxane, an aliphatic six-member ring with two oxygen atoms in ring positions 1 and 2. (+)-Angustanoic acid C is found in Illicium angustisepalum . Based on a literature review very few articles have been published on Angustanoic acid C.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 52 55  0  0  0  0  0  0  0  0999 V2000
    5.3452    0.4592    0.4372 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5667   -0.3024   -0.2738 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2127   -1.3309   -1.1820 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1134   -0.2169   -0.2442 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5303    0.7775    0.6859 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1915    0.8869    0.5400 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3735    1.8624    1.2436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0479    1.4450    1.4670 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4993    0.2916    0.6539 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9633    0.0945    0.5179 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3327   -1.4068    0.6566 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8266    0.7737    1.4879 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3944    1.4233    2.4386 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2302    0.7139    1.3778 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4994    0.4682   -0.8560 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8197   -0.2746   -1.9564 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4469   -0.7567   -1.6005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7616    0.1998   -0.6704 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8193    1.5743   -1.3161 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6617   -0.1227   -0.4303 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9922   -1.4606    0.1143 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5064   -1.5646    0.1954 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3496    0.0074   -1.6474 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6330   -0.0275   -1.5461 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0060    1.2264    1.1189 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4301    0.3424    0.3651 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4461   -2.2542   -0.5925 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1538   -0.9147   -1.5875 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4991   -1.6238   -1.9810 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0711    1.3610    1.4071 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8416    2.0311    2.2491 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4473    2.8483    0.7460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1849    1.1874    2.5491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6798    2.3287    1.2781 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1326   -0.6317    1.2134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3771   -1.9378    0.9414 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6234   -1.8160   -0.3259 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1159   -1.5711    1.3966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6030   -0.1974    1.1457 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5731    0.1073   -0.8451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5835    1.5607   -0.9966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8356    0.3736   -2.8722 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4040   -1.1905   -2.2686 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4309   -1.7868   -1.2512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8564   -0.7190   -2.5666 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2234    1.5158   -2.3705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3488    2.3258   -0.7231 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2154    1.9999   -1.4814 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6520   -2.3028   -0.5427 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6089   -1.6830    1.1160 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8594   -1.6967    1.2452 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9066   -2.3967   -0.3944 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  1  0
  2  1  2  3
  4  2  1  0
  4 22  1  0
 22 21  1  0
 21 20  1  0
 20 23  1  6
 23 24  1  0
 20  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  1
 10 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  6
 10 12  1  0
 12 14  1  0
 12 13  2  0
  6  5  2  0
  4 24  1  6
 18  9  1  0
  5  4  1  0
 18 20  1  0
  3 27  1  0
  3 28  1  0
  3 29  1  0
  1 25  1  0
  1 26  1  0
 22 51  1  0
 22 52  1  0
 21 49  1  0
 21 50  1  0
  7 31  1  0
  7 32  1  0
  8 33  1  0
  8 34  1  0
  9 35  1  1
 11 36  1  0
 11 37  1  0
 11 38  1  0
 15 40  1  0
 15 41  1  0
 16 42  1  0
 16 43  1  0
 17 44  1  0
 17 45  1  0
 19 46  1  0
 19 47  1  0
 19 48  1  0
 14 39  1  0
  5 30  1  0
M  END


  Mrv1652304292206032D          

 24 27  0  0  1  0            999 V2000
    1.0871   -1.0596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7497   -0.3706    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4056    0.4891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5118    0.7271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1654    0.0761    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2089   -0.7761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9747    0.2365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2404    1.0175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5182   -0.3842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5447    0.0824    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9994   -0.4814    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9394    1.1544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7891    1.1256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1307    0.3489    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6111   -0.2919    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9061   -1.0623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7209   -1.1920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2406   -0.5512    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9455    0.2192    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7052    0.5410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8063    1.3598    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3636    0.0440    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1035    1.0289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1750   -0.9922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  1  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  5 10  1  0  0  0  0
 10 11  1  0  0  0  0
  2 11  1  1  0  0  0
  3 12  1  0  0  0  0
 12 13  1  0  0  0  0
 14 13  1  1  0  0  0
 14 15  1  0  0  0  0
  2 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 14 19  1  0  0  0  0
 19 20  1  1  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 19 23  1  6  0  0  0
 15 24  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0082993

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=C)[C@]12CC[C@]3(OO1)C(CC[C@H]1[C@](C)(CCC[C@]31C)C(O)=O)=C2

> <INCHI_IDENTIFIER>
InChI=1S/C20H28O4/c1-13(2)19-10-11-20(24-23-19)14(12-19)6-7-15-17(3,16(21)22)8-5-9-18(15,20)4/h12,15H,1,5-11H2,2-4H3,(H,21,22)/t15-,17-,18-,19+,20-/m0/s1

> <INCHI_KEY>
WMBGNPQDZHRODL-XCZFOBESSA-N

> <FORMULA>
C20H28O4

> <MOLECULAR_WEIGHT>
332.44

> <EXACT_MASS>
332.198759382

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
36.95880791641756

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2S,6S,7R,12R)-2,6-dimethyl-12-(prop-1-en-2-yl)-13,14-dioxatetracyclo[10.2.2.0^{1,10}.0^{2,7}]hexadec-10-ene-6-carboxylic acid

> <ALOGPS_LOGP>
3.97

> <JCHEM_LOGP>
4.349587289333334

> <ALOGPS_LOGS>
-4.20

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.3086793798013465

> <JCHEM_PKA_STRONGEST_BASIC>
-4.899239372123917

> <JCHEM_POLAR_SURFACE_AREA>
55.760000000000005

> <JCHEM_REFRACTIVITY>
90.46109999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.09e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,6S,7R,12R)-2,6-dimethyl-12-(prop-1-en-2-yl)-13,14-dioxatetracyclo[10.2.2.0^{1,10}.0^{2,7}]hexadec-10-ene-6-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0       2.029  -1.978   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.266  -0.692   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.624   0.913   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.955   1.357   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.309   0.142   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.390  -1.449   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.819   0.441   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.315   1.899   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.834  -0.717   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       1.017   0.154   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0       1.866  -0.899   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       3.620   2.155   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.206   2.101   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.844   0.651   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.874  -0.545   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.425  -1.983   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.946  -2.225   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.916  -1.029   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.365   0.409   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.783   1.010   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       8.972   2.538   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      10.012   0.082   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       7.660   1.921   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.060  -1.852   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3   11   15                                             
CONECT    3    2    4   12                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7   10                                             
CONECT    6    5    1                                                       
CONECT    7    5    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    5   11                                                       
CONECT   11   10    2                                                       
CONECT   12    3   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   19                                                  
CONECT   15   14    2   16   24                                             
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   14   20   23                                             
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   19                                                            
CONECT   24   15                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   54    0
END

View in JSmol

Synonyms

Value	Source
Angustanoate C	Generator

Chemical Formula

C₂₀H₂₈O₄

Average Mass

332.4400 Da

Monoisotopic Mass

332.19876 Da

IUPAC Name

(1S,2S,6S,7R,12R)-2,6-dimethyl-12-(prop-1-en-2-yl)-13,14-dioxatetracyclo[10.2.2.0^{1,10}.0^{2,7}]hexadec-10-ene-6-carboxylic acid

Traditional Name

(1S,2S,6S,7R,12R)-2,6-dimethyl-12-(prop-1-en-2-yl)-13,14-dioxatetracyclo[10.2.2.0^{1,10}.0^{2,7}]hexadec-10-ene-6-carboxylic acid

CAS Registry Number

Not Available

SMILES

CC(=C)[C@]12CC[C@]3(OO1)C(CC[C@H]1[C@](C)(CCC[C@]31C)C(O)=O)=C2

InChI Identifier

InChI=1S/C20H28O4/c1-13(2)19-10-11-20(24-23-19)14(12-19)6-7-15-17(3,16(21)22)8-5-9-18(15,20)4/h12,15H,1,5-11H2,2-4H3,(H,21,22)/t15-,17-,18-,19+,20-/m0/s1

InChI Key

WMBGNPQDZHRODL-XCZFOBESSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Illicium angustisepalum	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 1,2-dioxanes. These are organic compounds containing 1,2-dioxane, an aliphatic six-member ring with two oxygen atoms in ring positions 1 and 2.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Dioxanes

Sub Class

1,2-dioxanes

Direct Parent

1,2-dioxanes

Alternative Parents

Substituents

Ortho-dioxane
Dialkyl peroxide
Oxacycle
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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	3.97	ALOGPS
logP	4.35	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	4.31	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	55.76 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	90.46 m³·mol⁻¹	ChemAxon
Polarizability	36.96 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

Not Available

KNApSAcK ID

C00049987

Chemspider ID

8743966

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10568579

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (+)-Angustanoic acid C (NP0082993)

MOL for NP0082993 ((+)-Angustanoic acid C)

3D MOL for NP0082993 ((+)-Angustanoic acid C)

3D SDF for NP0082993 ((+)-Angustanoic acid C)

3D-SDF for NP0082993 ((+)-Angustanoic acid C)

PDB for NP0082993 ((+)-Angustanoic acid C)

3D PDB for NP0082993 ((+)-Angustanoic acid C)

SMILES for NP0082993 ((+)-Angustanoic acid C)

INCHI for NP0082993 ((+)-Angustanoic acid C)

Structure for NP0082993 ((+)-Angustanoic acid C)

3D Structure for NP0082993 ((+)-Angustanoic acid C)