NP-MRD: Showing NP-Card for Hirsutidin (NP0054452)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-28 00:48:14 UTC

Updated at

2022-04-28 00:48:14 UTC

NP-MRD ID

NP0054452

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Hirsutidin

Description

Hirsutidin belongs to the class of organic compounds known as 7-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C7 atom of the flavonoid backbone. Thus, hirsutidin is considered to be a flavonoid. Hirsutidin is a secondary metabolite. Secondary metabolites are metabolically or physiologically non-essential metabolites that may serve a role as defense or signalling molecules. In some cases they are simply molecules that arise from the incomplete metabolism of other secondary metabolites. Hirsutidin is found in Catharanthus roseus, Catharanthus roseus G.Don. and Primula hirsuta. Hirsutidin was first documented in 2003 (PMID: 12628396). Based on a literature review very few articles have been published on hirsutidin (PMID: 34146990).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 42 44  0  0  0  0  0  0  0  0999 V2000
    6.3348    1.8195   -1.1754 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9478    1.9713   -1.1112 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1129    0.9572   -0.6610 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6577   -0.2296   -0.2665 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8179   -1.2414    0.1833 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3593   -2.4395    0.5822 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4555   -1.0612    0.2348 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5880   -2.0296    0.6708 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2222   -1.7402    0.6820 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6009   -2.7488    1.1291 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2828   -0.5473    0.2818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6902   -0.1624    0.2610 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7256   -0.9572    0.6470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0391   -0.5119    0.5956 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0466   -1.3574    0.9980 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7522   -2.6535    1.4548 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3780    0.7334    0.1616 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6633    1.2199    0.0924 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3239    1.5471   -0.2331 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6344    2.8301   -0.6836 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5711    3.6656   -1.0871 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0233    1.1261   -0.1896 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6003    0.3416   -0.1260 O   0  0  0  0  0  3  0  0  0  0  0  0
    1.8931    0.1464   -0.1659 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7594    1.1420   -0.6120 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6533    0.9338   -1.7916 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7908    2.7031   -1.6518 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8118    1.6749   -0.1808 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7246   -0.3923   -0.2988 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8345   -3.2009    0.9114 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9274   -2.9950    1.0007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2614   -3.6241    1.4255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5367   -1.9665    1.0062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6293   -3.2729    1.6332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1346   -3.1932    0.6851 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1124   -2.6065    2.3594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4379    0.6320    0.3786 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0775    3.2097   -1.9814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9185    4.6646   -1.3882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7783    3.7392   -0.2854 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2040    1.7946   -0.5098 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3305    2.0795   -0.9237 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  5  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
  9 11  1  0
 11 23  2  0
 23 24  1  0
 24 25  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 14 17  2  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 20 21  1  0
 19 22  2  0
 25  3  1  0
 22 12  1  0
 24  7  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  4 29  1  0
  6 30  1  0
  8 31  1  0
 10 32  1  0
 25 42  1  0
 13 33  1  0
 16 34  1  0
 16 35  1  0
 16 36  1  0
 18 37  1  0
 21 38  1  0
 21 39  1  0
 21 40  1  0
 22 41  1  0
M  CHG  1  23   1
M  END

  Mrv1652304282202482D          

 25 27  0  0  0  0            999 V2000
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    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
    1.4289   -0.0000    0.0000 O   0  3  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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  2  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  4 10  1  0  0  0  0
  9 11  1  0  0  0  0
  8 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 12 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 15 20  1  0  0  0  0
 14 21  1  0  0  0  0
 21 22  1  0  0  0  0
  3 23  1  0  0  0  0
  1 24  1  0  0  0  0
 24 25  1  0  0  0  0
M  CHG  1   7   1
M  END
> <DATABASE_ID>
NP0054452

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(O)=C2C=C(O)C(=[O+]C2=C1)C1=CC(OC)=C(O)C(OC)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C18H16O7/c1-22-10-6-12(19)11-8-13(20)18(25-14(11)7-10)9-4-15(23-2)17(21)16(5-9)24-3/h4-8H,1-3H3,(H2-,19,20,21)/p+1

> <INCHI_KEY>
JGPCLGHKWGCWNO-UHFFFAOYSA-O

> <FORMULA>
C18H17O7

> <MOLECULAR_WEIGHT>
345.326

> <EXACT_MASS>
345.096879308

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
35.196417070616526

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
1

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3,5-dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-7-methoxy-1lambda4-chromen-1-ylium

> <ALOGPS_LOGP>
2.85

> <JCHEM_LOGP>
2.8609999999999993

> <ALOGPS_LOGS>
-4.36

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
6.920568078552447

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.028259196322986

> <JCHEM_PKA_STRONGEST_BASIC>
-4.42380563694946

> <JCHEM_POLAR_SURFACE_AREA>
101.52000000000002

> <JCHEM_REFRACTIVITY>
99.54090000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.65e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3,5-dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-7-methoxy-1lambda4-chromen-1-ylium

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.667  -0.000   0.000  0.00  0.00           O+1
HETATM    8  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       5.335  -0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.002  -0.000   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       9.336  -0.770   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      10.669  -0.000   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       9.336   2.310   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       6.668   3.850   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       8.002   4.620   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       0.000  -4.620   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      -2.667   0.000   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -4.001  -0.770   0.000  0.00  0.00           C+0
CONECT    1    2    6   24                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4   23                                                  
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8                                                       
CONECT    8    7    9   12                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9    4                                                       
CONECT   11    9                                                            
CONECT   12    8   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   21                                                  
CONECT   15   14   16   20                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16   12                                                       
CONECT   18   16   19                                                       
CONECT   19   18                                                            
CONECT   20   15                                                            
CONECT   21   14   22                                                       
CONECT   22   21                                                            
CONECT   23    3                                                            
CONECT   24    1   25                                                       
CONECT   25   24                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₁₇O₇

Average Mass

345.3260 Da

Monoisotopic Mass

345.09688 Da

IUPAC Name

3,5-dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-7-methoxy-1lambda4-chromen-1-ylium

Traditional Name

3,5-dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-7-methoxy-1lambda4-chromen-1-ylium

CAS Registry Number

Not Available

SMILES

COC1=CC(O)=C2C=C(O)C(=[O+]C2=C1)C1=CC(OC)=C(O)C(OC)=C1

InChI Identifier

InChI=1S/C18H16O7/c1-22-10-6-12(19)11-8-13(20)18(25-14(11)7-10)9-4-15(23-2)17(21)16(5-9)24-3/h4-8H,1-3H3,(H2-,19,20,21)/p+1

InChI Key

JGPCLGHKWGCWNO-UHFFFAOYSA-O

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
Catharanthus roseus	LOTUS Database	35616633
Catharanthus roseus G.Don.	Plant	KNApSAcK
Primula hirsuta	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 7-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C7 atom of the flavonoid backbone.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

O-methylated flavonoids

Direct Parent

7-O-methylated flavonoids

Alternative Parents

Substituents

3p-methoxyflavonoid-skeleton
7-methoxyflavonoid-skeleton
3-hydroxyflavonoid
4'-hydroxyflavonoid
5-hydroxyflavonoid
Hydroxyflavonoid
Anthocyanidin
Benzopyran
Methoxyphenol
1-benzopyran
Dimethoxybenzene
M-dimethoxybenzene
Methoxybenzene
Phenol ether
Anisole
Phenoxy compound
1-hydroxy-2-unsubstituted benzenoid
Phenol
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
Benzenoid
Monocyclic benzene moiety
Heteroaromatic compound
Oxacycle
Organoheterocyclic compound
Ether
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
Organic cation
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

anthocyanidin cation (CHEBI:5728 )
Anthocyanidins (C08643 )
Anthocyanidins (LMPK12010421 )

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	2.85	ALOGPS
logP	2.86	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	6.03	ChemAxon
pKa (Strongest Basic)	-4.4	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	101.52 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	99.54 m³·mol⁻¹	ChemAxon
Polarizability	35.2 Å³	ChemAxon
Number of Rings	3	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

C00006619

Chemspider ID

390303

KEGG Compound ID

C08643

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Hirsutidin

METLIN ID

Not Available

PubChem Compound

441694

PDB ID

Not Available

ChEBI ID

5728

Good Scents ID

Not Available

References

General References

Tatsuzawa F, Mizuno T, Kikuchi R, Kato K, Ota T, Murai Y, Yangzom R, Iwashina T: Flavonoids in the flowers of Primula xpolyantha Mill. and Primula primulina (Spreng.) H. Hara (Primulaceae). Phytochemistry. 2021 Sep;189:112827. doi: 10.1016/j.phytochem.2021.112827. Epub 2021 Jun 16. [PubMed:34146990 ]
Filippini R, Caniato R, Piovan A, Cappelletti EM: Production of anthocyanins by Catharanthus roseus. Fitoterapia. 2003 Feb;74(1-2):62-7. doi: 10.1016/s0367-326x(02)00296-4. [PubMed:12628396 ]

Showing NP-Card for Hirsutidin (NP0054452)

MOL for NP0054452 (Hirsutidin)

3D MOL for NP0054452 (Hirsutidin)

3D SDF for NP0054452 (Hirsutidin)

3D-SDF for NP0054452 (Hirsutidin)

PDB for NP0054452 (Hirsutidin)

3D PDB for NP0054452 (Hirsutidin)

SMILES for NP0054452 (Hirsutidin)

INCHI for NP0054452 (Hirsutidin)

Structure for NP0054452 (Hirsutidin)

3D Structure for NP0054452 (Hirsutidin)