NP-MRD: Showing NP-Card for Pyrethroidinin (NP0063932)

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Record Information

Version

1.0

Created at

2022-04-28 08:14:57 UTC

Updated at

2022-04-28 08:14:57 UTC

NP-MRD ID

NP0063932

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Pyrethroidinin

Description

(3AS,6R,6aR,8R,9bS)-6,8-dihydroxy-6,9-dimethyl-3-methylidene-2H,3H,3aH,4H,5H,6H,6aH,7H,8H,9bH-azuleno[4,5-b]furan-2-one belongs to the class of organic compounds known as gamma butyrolactones. Gamma butyrolactones are compounds containing a gamma butyrolactone moiety, which consists of an aliphatic five-member ring with four carbon atoms, one oxygen atom, and bears a ketone group on the carbon adjacent to the oxygen atom. Pyrethroidinin is found in Pyrethrum pyrethroides and Tanacetum densum. It was first documented in 2022 (PMID: 35483916). Based on a literature review a significant number of articles have been published on (3aS,6R,6aR,8R,9bS)-6,8-dihydroxy-6,9-dimethyl-3-methylidene-2H,3H,3aH,4H,5H,6H,6aH,7H,8H,9bH-azuleno[4,5-b]furan-2-one (PMID: 35483915) (PMID: 35483914) (PMID: 35483913) (PMID: 35483912).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 39 41  0  0  0  0  0  0  0  0999 V2000
    3.3783   -2.5359    0.5755 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8134   -1.3626    0.3817 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4250   -0.0966    0.0020 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6438    0.0787   -0.1990 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3888    0.8553   -0.0877 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2218    0.1434   -0.3901 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0231    0.8712   -0.0127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1270    2.1695   -0.2805 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8812    3.0439   -0.9400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4622    2.6790    0.1885 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3578    3.2543    1.4535 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2775    1.4046    0.2046 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2393    0.3933    0.6445 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7033   -0.9594    0.1811 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8834   -1.0379   -1.2979 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9738   -1.1646    0.7645 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8367   -2.0873    0.6536 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4941   -2.1536   -0.0632 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3675   -1.0847    0.5191 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4585   -2.6857    0.4595 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8293   -3.4207    0.8579 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1892   -0.2254   -1.4199 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4274    3.8850   -1.4825 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3695    2.4040   -1.7281 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6605    3.3399   -0.2128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9010    3.3824   -0.5484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6787    2.6976    1.9458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5541    1.1877   -0.8553 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1362    1.4543    0.8808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2049    0.4185    1.7427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9316   -0.7533   -1.5638 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1562   -0.4596   -1.8719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8101   -2.1265   -1.5836 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6373   -0.5212    0.4436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6096   -2.0327    1.7371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3684   -3.0349    0.4254 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9565   -3.1354    0.0521 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2737   -1.9644   -1.1431 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0937   -0.8202    1.5667 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0
  8  7  2  0
  7  6  1  0
  6  5  1  0
  5  3  1  0
  3  4  2  0
  3  2  1  0
  2  1  2  3
  2 19  1  0
 19 18  1  0
 18 17  1  0
 17 14  1  0
 14 15  1  0
 14 16  1  1
 14 13  1  0
 13 12  1  0
 12 10  1  0
 10 11  1  0
 10  8  1  0
 13  7  1  0
 19  6  1  0
  9 23  1  0
  9 24  1  0
  9 25  1  0
  6 22  1  6
  1 20  1  0
  1 21  1  0
 19 39  1  1
 18 37  1  0
 18 38  1  0
 17 35  1  0
 17 36  1  0
 15 31  1  0
 15 32  1  0
 15 33  1  0
 16 34  1  0
 13 30  1  1
 12 28  1  0
 12 29  1  0
 10 26  1  6
 11 27  1  0
M  END


  Mrv1652304282210142D          

 19 21  0  0  1  0            999 V2000
    2.0090    2.2026    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4946    1.5576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9491    0.8690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7444    1.0885    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7814    1.9127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3894    0.5741    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6592    0.0966    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6696    1.5576    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1552    2.2026    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3388    3.0069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0821    3.3648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8254    3.0069    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1666    3.7580    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6336    3.1724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6172    1.9127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3057    2.3672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5802    1.0885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2252    0.5741    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2151    0.8690    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  6  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  1  5  1  0  0  0  0
  4  6  1  1  0  0  0
  3  7  1  0  0  0  0
  2  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  1 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  6  0  0  0
  9 15  1  6  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
  8 19  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0063932

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=C2[C@H]3OC(=O)C(=C)[C@@H]3CC[C@@](C)(O)[C@@H]2C[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C15H20O4/c1-7-9-4-5-15(3,18)10-6-11(16)8(2)12(10)13(9)19-14(7)17/h9-11,13,16,18H,1,4-6H2,2-3H3/t9-,10+,11+,13-,15+/m0/s1

> <INCHI_KEY>
ZHDDWGCKBPKENN-UKKPDTPPSA-N

> <FORMULA>
C15H20O4

> <MOLECULAR_WEIGHT>
264.321

> <EXACT_MASS>
264.136159124

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
28.259751143094462

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3aS,6R,6aR,8R,9bS)-6,8-dihydroxy-6,9-dimethyl-3-methylidene-2H,3H,3aH,4H,5H,6H,6aH,7H,8H,9bH-azuleno[4,5-b]furan-2-one

> <ALOGPS_LOGP>
0.79

> <JCHEM_LOGP>
0.8532449713333332

> <ALOGPS_LOGS>
-1.70

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.95352502746459

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.33474604189566

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9263236998105118

> <JCHEM_POLAR_SURFACE_AREA>
66.76

> <JCHEM_REFRACTIVITY>
70.12039999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.23e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3aS,6R,6aR,8R,9bS)-6,8-dihydroxy-6,9-dimethyl-3-methylidene-3aH,4H,5H,6aH,7H,8H,9bH-azuleno[4,5-b]furan-2-one

> <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       3.750   4.111   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.790   2.907   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.638   1.622   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.123   2.032   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.192   3.570   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       6.327   1.072   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       3.097   0.180   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.250   2.907   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.290   4.111   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.632   5.613   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.020   6.281   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.407   5.613   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       4.044   7.015   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       4.916   5.922   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.152   3.570   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.437   4.419   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.083   2.032   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -2.287   1.072   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       0.402   1.622   0.000  0.00  0.00           O+0
CONECT    1    2    5   12                                                  
CONECT    2    1    3    8                                                  
CONECT    3    2    4    7                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4    1                                                       
CONECT    6    4                                                            
CONECT    7    3                                                            
CONECT    8    2    9   19                                                  
CONECT    9    8   10   15                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11    1   13   14                                             
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15    9   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17    8                                                       
MASTER        0    0    0    0    0    0    0    0   19    0   42    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₀O₄

Average Mass

264.3210 Da

Monoisotopic Mass

264.13616 Da

IUPAC Name

(3aS,6R,6aR,8R,9bS)-6,8-dihydroxy-6,9-dimethyl-3-methylidene-2H,3H,3aH,4H,5H,6H,6aH,7H,8H,9bH-azuleno[4,5-b]furan-2-one

Traditional Name

(3aS,6R,6aR,8R,9bS)-6,8-dihydroxy-6,9-dimethyl-3-methylidene-3aH,4H,5H,6aH,7H,8H,9bH-azuleno[4,5-b]furan-2-one

CAS Registry Number

Not Available

SMILES

CC1=C2[C@H]3OC(=O)C(=C)[C@@H]3CC[C@@](C)(O)[C@@H]2C[C@H]1O

InChI Identifier

InChI=1S/C15H20O4/c1-7-9-4-5-15(3,18)10-6-11(16)8(2)12(10)13(9)19-14(7)17/h9-11,13,16,18H,1,4-6H2,2-3H3/t9-,10+,11+,13-,15+/m0/s1

InChI Key

ZHDDWGCKBPKENN-UKKPDTPPSA-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
Pyrethrum pyrethroides	-	KNApSAcK
Tanacetum densum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as gamma butyrolactones. Gamma butyrolactones are compounds containing a gamma butyrolactone moiety, which consists of an aliphatic five-member ring with four carbon atoms, one oxygen atom, and bears a ketone group on the carbon adjacent to the oxygen atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Lactones

Sub Class

Gamma butyrolactones

Direct Parent

Gamma butyrolactones

Alternative Parents

Substituents

Gamma butyrolactone
Cyclic alcohol
Tertiary alcohol
Tetrahydrofuran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Secondary alcohol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Oxacycle
Organooxygen compound
Organic oxide
Organic oxygen compound
Alcohol
Carbonyl group
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	0.79	ALOGPS
logP	0.85	ChemAxon
logS	-1.7	ALOGPS
pKa (Strongest Acidic)	14.33	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.76 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	70.12 m³·mol⁻¹	ChemAxon
Polarizability	28.26 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

Not Available

Chemspider ID

10297942

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

21680577

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Uchida Y, Kan H, Sakurai K, Horimoto Y, Hayashi E, Iida A, Okamura N, Oishi K, Matsukawa N: APOE varepsilon4 dose associates with increased brain iron and beta-amyloid via blood-brain barrier dysfunction. J Neurol Neurosurg Psychiatry. 2022 Apr 28. pii: jnnp-2021-328519. doi: 10.1136/jnnp-2021-328519. [PubMed:35483916 ]
Cacciaguerra L, Pagani E, Radaelli M, Mesaros S, Martinelli V, Ivanovic J, Drulovic J, Filippi M, Rocca MA: MR T2-relaxation time as an indirect measure of brain water content and disease activity in NMOSD. J Neurol Neurosurg Psychiatry. 2022 Apr 28. pii: jnnp-2022-328956. doi: 10.1136/jnnp-2022-328956. [PubMed:35483915 ]
Broomfield NM, West R, Barber M, Quinn TJ, Gillespie D, Walters M, House A: TEARS: a longitudinal investigation of the prevalence, psychological associations and trajectory of poststroke emotionalism. J Neurol Neurosurg Psychiatry. 2022 Apr 28. pii: jnnp-2022-329042. doi: 10.1136/jnnp-2022-329042. [PubMed:35483914 ]
Khankari J, Yu Y, Ouyang J, Hussein R, Do HM, Heit JJ, Zaharchuk G: Automated detection of arterial landmarks and vascular occlusions in patients with acute stroke receiving digital subtraction angiography using deep learning. J Neurointerv Surg. 2022 Apr 28. pii: neurintsurg-2021-018638. doi: 10.1136/neurintsurg-2021-018638. [PubMed:35483913 ]
Adeeb N, Dibas M, Diestro JDB, Phan K, Cuellar-Saenz HH, Sweid A, Lay SV, Guenego A, Aslan A, Renieri L, Sundararajan SH, Saliou G, Mohlenbruch M, Regenhardt RW, Vranic JE, Lylyk I, Foreman PM, Vachhani JA, Zupancic V, Hafeez MU, Rutledge C, Waqas M, Tutino VM, Rabinov JD, Ren Y, Schirmer CM, Piano M, Kuhn AL, Michelozzi C, Elens S, Starke RM, Hassan A, Salehani A, Brehm A, MohammedAli M, Jones J, Psychogios M, Spears J, Lubicz B, Panni P, Puri AS, Pero G, Griessenauer CJ, Asadi H, Siddiqui A, Ducruet A, Albuquerque FC, Du R, Kan P, Kalousek V, Lylyk P, Stapleton CJ, Boddu S, Knopman J, Aziz-Sultan MA, Limbucci N, Jabbour P, Cognard C, Patel AB, Dmytriw AA: Comparing treatment outcomes of various intracranial bifurcation aneurysms locations using the Woven EndoBridge (WEB) device. J Neurointerv Surg. 2022 Apr 28. pii: neurintsurg-2022-018694. doi: 10.1136/neurintsurg-2022-018694. [PubMed:35483912 ]

Showing NP-Card for Pyrethroidinin (NP0063932)

MOL for NP0063932 (Pyrethroidinin)

3D MOL for NP0063932 (Pyrethroidinin)

3D SDF for NP0063932 (Pyrethroidinin)

3D-SDF for NP0063932 (Pyrethroidinin)

PDB for NP0063932 (Pyrethroidinin)

3D PDB for NP0063932 (Pyrethroidinin)

SMILES for NP0063932 (Pyrethroidinin)

INCHI for NP0063932 (Pyrethroidinin)

Structure for NP0063932 (Pyrethroidinin)

3D Structure for NP0063932 (Pyrethroidinin)