NP-MRD: Showing NP-Card for cordysinin E (NP0036201)

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Record Information

Version

2.0

Created at

2021-06-20 19:26:13 UTC

Updated at

2021-06-30 00:07:44 UTC

NP-MRD ID

NP0036201

Secondary Accession Numbers

None

Natural Product Identification

Common Name

cordysinin E

Provided By

JEOL Database JEOL Logo

Description

Cordysinin E 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. cordysinin E is found in Cordyceps sinensis. cordysinin E was first documented in 2011 (Yang, M. -L., et al.). Based on a literature review very few articles have been published on cordysinin E.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202121263D          

 32 34  0  0  0  0            999 V2000
   -4.1547   -3.6657    0.5936 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2335   -4.2450   -0.3381 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9973   -4.6959    0.4461 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4398   -3.5644    1.1425 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9291   -5.3844   -0.4057 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5507   -4.6422   -1.6591 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8639   -5.2186   -2.8534 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5060   -4.6100   -4.0060 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1645   -3.4005   -4.0883 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4741   -2.7730   -2.8740 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1047   -3.4064   -1.6906 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4882   -2.5823   -0.6565 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1147   -1.4549   -1.1294 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6588   -0.3672   -0.4369 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2382    0.6562   -1.1925 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2674    0.5930   -2.5837 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7137   -0.5005   -3.2600 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1247   -1.5474   -2.5207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9327   -3.3917    0.0751 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7184   -5.0886   -0.8381 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9901   -3.4673   -1.0680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3102   -5.3898    1.2360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2237   -3.1261    1.5379 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2904   -6.3811   -0.6881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0183   -5.5297    0.1882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7830   -5.1467   -4.9096 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4253   -2.9640   -5.0439 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2709   -2.7690    0.3163 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6358   -0.3157    0.6469 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6722    1.5146   -0.6847 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7228    1.4005   -3.1517 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7384   -0.5389   -4.3447 H   0  0  0  0  0  0  0  0  0  0  0  0
 10 18  1  0  0  0  0
 13 18  2  0  0  0  0
 11  6  2  0  0  0  0
 18 17  1  0  0  0  0
 13 12  1  0  0  0  0
 17 16  2  0  0  0  0
  6  7  1  0  0  0  0
 16 15  1  0  0  0  0
 12 11  1  0  0  0  0
 15 14  2  0  0  0  0
 14 13  1  0  0  0  0
  7  8  2  0  0  0  0
  6  5  1  0  0  0  0
  5  3  1  0  0  0  0
  8  9  1  0  0  0  0
  3  2  1  0  0  0  0
  9 10  2  0  0  0  0
  2  1  1  0  0  0  0
 10 11  1  0  0  0  0
  3  4  1  0  0  0  0
 12 28  1  0  0  0  0
  8 26  1  0  0  0  0
  9 27  1  0  0  0  0
 17 32  1  0  0  0  0
 16 31  1  0  0  0  0
 15 30  1  0  0  0  0
 14 29  1  0  0  0  0
  5 24  1  0  0  0  0
  5 25  1  0  0  0  0
  3 22  1  1  0  0  0
  2 20  1  0  0  0  0
  2 21  1  0  0  0  0
  1 19  1  0  0  0  0
  4 23  1  0  0  0  0
M  END

     RDKit          3D

 32 34  0  0  0  0  0  0  0  0999 V2000
   -4.1547   -3.6657    0.5936 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2335   -4.2450   -0.3381 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9973   -4.6959    0.4461 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4398   -3.5644    1.1425 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9291   -5.3844   -0.4057 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5507   -4.6422   -1.6591 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8639   -5.2186   -2.8534 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5060   -4.6100   -4.0060 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1645   -3.4005   -4.0883 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4741   -2.7730   -2.8740 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1047   -3.4064   -1.6906 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4882   -2.5823   -0.6565 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1147   -1.4549   -1.1294 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6588   -0.3672   -0.4369 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2382    0.6562   -1.1925 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2674    0.5930   -2.5837 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7137   -0.5005   -3.2600 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1247   -1.5474   -2.5207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9327   -3.3917    0.0751 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7184   -5.0886   -0.8381 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9901   -3.4673   -1.0680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3102   -5.3898    1.2360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2237   -3.1261    1.5379 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2904   -6.3811   -0.6881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0183   -5.5297    0.1882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7830   -5.1467   -4.9096 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4253   -2.9640   -5.0439 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2709   -2.7690    0.3163 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6358   -0.3157    0.6469 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6722    1.5146   -0.6847 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7228    1.4005   -3.1517 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7384   -0.5389   -4.3447 H   0  0  0  0  0  0  0  0  0  0  0  0
 10 18  1  0
 13 18  2  0
 11  6  2  0
 18 17  1  0
 13 12  1  0
 17 16  2  0
  6  7  1  0
 16 15  1  0
 12 11  1  0
 15 14  2  0
 14 13  1  0
  7  8  2  0
  6  5  1  0
  5  3  1  0
  8  9  1  0
  3  2  1  0
  9 10  2  0
  2  1  1  0
 10 11  1  0
  3  4  1  0
 12 28  1  0
  8 26  1  0
  9 27  1  0
 17 32  1  0
 16 31  1  0
 15 30  1  0
 14 29  1  0
  5 24  1  0
  5 25  1  0
  3 22  1  1
  2 20  1  0
  2 21  1  0
  1 19  1  0
  4 23  1  0
M  END


  Mrv1652306202121263D          

 32 34  0  0  0  0            999 V2000
   -4.1547   -3.6657    0.5936 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2335   -4.2450   -0.3381 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9973   -4.6959    0.4461 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4398   -3.5644    1.1425 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9291   -5.3844   -0.4057 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5507   -4.6422   -1.6591 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8639   -5.2186   -2.8534 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5060   -4.6100   -4.0060 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1645   -3.4005   -4.0883 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4741   -2.7730   -2.8740 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1047   -3.4064   -1.6906 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4882   -2.5823   -0.6565 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1147   -1.4549   -1.1294 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6588   -0.3672   -0.4369 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2382    0.6562   -1.1925 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2674    0.5930   -2.5837 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7137   -0.5005   -3.2600 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1247   -1.5474   -2.5207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9327   -3.3917    0.0751 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7184   -5.0886   -0.8381 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9901   -3.4673   -1.0680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3102   -5.3898    1.2360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2237   -3.1261    1.5379 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2904   -6.3811   -0.6881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0183   -5.5297    0.1882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7830   -5.1467   -4.9096 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4253   -2.9640   -5.0439 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2709   -2.7690    0.3163 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6358   -0.3157    0.6469 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6722    1.5146   -0.6847 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7228    1.4005   -3.1517 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7384   -0.5389   -4.3447 H   0  0  0  0  0  0  0  0  0  0  0  0
 10 18  1  0  0  0  0
 13 18  2  0  0  0  0
 11  6  2  0  0  0  0
 18 17  1  0  0  0  0
 13 12  1  0  0  0  0
 17 16  2  0  0  0  0
  6  7  1  0  0  0  0
 16 15  1  0  0  0  0
 12 11  1  0  0  0  0
 15 14  2  0  0  0  0
 14 13  1  0  0  0  0
  7  8  2  0  0  0  0
  6  5  1  0  0  0  0
  5  3  1  0  0  0  0
  8  9  1  0  0  0  0
  3  2  1  0  0  0  0
  9 10  2  0  0  0  0
  2  1  1  0  0  0  0
 10 11  1  0  0  0  0
  3  4  1  0  0  0  0
 12 28  1  0  0  0  0
  8 26  1  0  0  0  0
  9 27  1  0  0  0  0
 17 32  1  0  0  0  0
 16 31  1  0  0  0  0
 15 30  1  0  0  0  0
 14 29  1  0  0  0  0
  5 24  1  0  0  0  0
  5 25  1  0  0  0  0
  3 22  1  1  0  0  0
  2 20  1  0  0  0  0
  2 21  1  0  0  0  0
  1 19  1  0  0  0  0
  4 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0036201

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC([H])([H])[C@]([H])(O[H])C([H])([H])C1=C2N([H])C3=C(C([H])=C([H])C([H])=C3[H])C2=C([H])C([H])=N1

> <INCHI_IDENTIFIER>
InChI=1S/C14H14N2O2/c17-8-9(18)7-13-14-11(5-6-15-13)10-3-1-2-4-12(10)16-14/h1-6,9,16-18H,7-8H2/t9-/m1/s1

> <INCHI_KEY>
OYZWACRLCWKSSL-SECBINFHSA-N

> <FORMULA>
C14H14N2O2

> <MOLECULAR_WEIGHT>
242.278

> <EXACT_MASS>
242.105527699

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
32

> <JCHEM_AVERAGE_POLARIZABILITY>
25.907254290401823

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R)-3-{9H-pyrido[3,4-b]indol-1-yl}propane-1,2-diol

> <ALOGPS_LOGP>
1.33

> <JCHEM_LOGP>
0.7940131796666665

> <ALOGPS_LOGS>
-2.95

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.22637131582723

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.395099798010172

> <JCHEM_PKA_STRONGEST_BASIC>
5.384305828524423

> <JCHEM_POLAR_SURFACE_AREA>
69.14

> <JCHEM_REFRACTIVITY>
68.2709

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.70e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R)-3-{9H-pyrido[3,4-b]indol-1-yl}propane-1,2-diol

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 32 34  0  0  0  0  0  0  0  0999 V2000
   -4.1547   -3.6657    0.5936 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2335   -4.2450   -0.3381 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9973   -4.6959    0.4461 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4398   -3.5644    1.1425 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9291   -5.3844   -0.4057 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5507   -4.6422   -1.6591 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8639   -5.2186   -2.8534 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5060   -4.6100   -4.0060 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1645   -3.4005   -4.0883 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4741   -2.7730   -2.8740 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1047   -3.4064   -1.6906 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4882   -2.5823   -0.6565 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1147   -1.4549   -1.1294 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6588   -0.3672   -0.4369 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2382    0.6562   -1.1925 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2674    0.5930   -2.5837 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7137   -0.5005   -3.2600 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1247   -1.5474   -2.5207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9327   -3.3917    0.0751 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7184   -5.0886   -0.8381 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9901   -3.4673   -1.0680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3102   -5.3898    1.2360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2237   -3.1261    1.5379 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2904   -6.3811   -0.6881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0183   -5.5297    0.1882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7830   -5.1467   -4.9096 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4253   -2.9640   -5.0439 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2709   -2.7690    0.3163 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6358   -0.3157    0.6469 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6722    1.5146   -0.6847 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7228    1.4005   -3.1517 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7384   -0.5389   -4.3447 H   0  0  0  0  0  0  0  0  0  0  0  0
 10 18  1  0
 13 18  2  0
 11  6  2  0
 18 17  1  0
 13 12  1  0
 17 16  2  0
  6  7  1  0
 16 15  1  0
 12 11  1  0
 15 14  2  0
 14 13  1  0
  7  8  2  0
  6  5  1  0
  5  3  1  0
  8  9  1  0
  3  2  1  0
  9 10  2  0
  2  1  1  0
 10 11  1  0
  3  4  1  0
 12 28  1  0
  8 26  1  0
  9 27  1  0
 17 32  1  0
 16 31  1  0
 15 30  1  0
 14 29  1  0
  5 24  1  0
  5 25  1  0
  3 22  1  1
  2 20  1  0
  2 21  1  0
  1 19  1  0
  4 23  1  0
M  END

HEADER    PROTEIN                                 20-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-JUN-21         0                                  
HETATM    1  O   UNK     0      -4.155  -3.666   0.594  0.00  0.00           O+0
HETATM    2  C   UNK     0      -3.233  -4.245  -0.338  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.997  -4.696   0.446  0.00  0.00           C+0
HETATM    4  O   UNK     0      -1.440  -3.564   1.143  0.00  0.00           O+0
HETATM    5  C   UNK     0      -0.929  -5.384  -0.406  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.551  -4.642  -1.659  0.00  0.00           C+0
HETATM    7  N   UNK     0      -0.864  -5.219  -2.853  0.00  0.00           N+0
HETATM    8  C   UNK     0      -0.506  -4.610  -4.006  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.165  -3.401  -4.088  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.474  -2.773  -2.874  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.105  -3.406  -1.691  0.00  0.00           C+0
HETATM   12  N   UNK     0       0.488  -2.582  -0.657  0.00  0.00           N+0
HETATM   13  C   UNK     0       1.115  -1.455  -1.129  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.659  -0.367  -0.437  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.238   0.656  -1.192  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.267   0.593  -2.584  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.714  -0.500  -3.260  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.125  -1.547  -2.521  0.00  0.00           C+0
HETATM   19  H   UNK     0      -4.933  -3.392   0.075  0.00  0.00           H+0
HETATM   20  H   UNK     0      -3.718  -5.089  -0.838  0.00  0.00           H+0
HETATM   21  H   UNK     0      -2.990  -3.467  -1.068  0.00  0.00           H+0
HETATM   22  H   UNK     0      -2.310  -5.390   1.236  0.00  0.00           H+0
HETATM   23  H   UNK     0      -2.224  -3.126   1.538  0.00  0.00           H+0
HETATM   24  H   UNK     0      -1.290  -6.381  -0.688  0.00  0.00           H+0
HETATM   25  H   UNK     0      -0.018  -5.530   0.188  0.00  0.00           H+0
HETATM   26  H   UNK     0      -0.783  -5.147  -4.910  0.00  0.00           H+0
HETATM   27  H   UNK     0       0.425  -2.964  -5.044  0.00  0.00           H+0
HETATM   28  H   UNK     0       0.271  -2.769   0.316  0.00  0.00           H+0
HETATM   29  H   UNK     0       1.636  -0.316   0.647  0.00  0.00           H+0
HETATM   30  H   UNK     0       2.672   1.515  -0.685  0.00  0.00           H+0
HETATM   31  H   UNK     0       2.723   1.401  -3.152  0.00  0.00           H+0
HETATM   32  H   UNK     0       1.738  -0.539  -4.345  0.00  0.00           H+0
CONECT    1    2   19                                                       
CONECT    2    3    1   20   21                                             
CONECT    3    5    2    4   22                                             
CONECT    4    3   23                                                       
CONECT    5    6    3   24   25                                             
CONECT    6   11    7    5                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   26                                                  
CONECT    9    8   10   27                                                  
CONECT   10   18    9   11                                                  
CONECT   11    6   12   10                                                  
CONECT   12   13   11   28                                                  
CONECT   13   18   12   14                                                  
CONECT   14   15   13   29                                                  
CONECT   15   16   14   30                                                  
CONECT   16   17   15   31                                                  
CONECT   17   18   16   32                                                  
CONECT   18   10   13   17                                                  
CONECT   19    1                                                            
CONECT   20    2                                                            
CONECT   21    2                                                            
CONECT   22    3                                                            
CONECT   23    4                                                            
CONECT   24    5                                                            
CONECT   25    5                                                            
CONECT   26    8                                                            
CONECT   27    9                                                            
CONECT   28   12                                                            
CONECT   29   14                                                            
CONECT   30   15                                                            
CONECT   31   16                                                            
CONECT   32   17                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   68    0
END

RDKit          3D

32 34  0  0  0  0  0  0  0  0999 V2000
   -4.1547   -3.6657    0.5936 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2335   -4.2450   -0.3381 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9973   -4.6959    0.4461 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4398   -3.5644    1.1425 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9291   -5.3844   -0.4057 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5507   -4.6422   -1.6591 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8639   -5.2186   -2.8534 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5060   -4.6100   -4.0060 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1645   -3.4005   -4.0883 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4741   -2.7730   -2.8740 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1047   -3.4064   -1.6906 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4882   -2.5823   -0.6565 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1147   -1.4549   -1.1294 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6588   -0.3672   -0.4369 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2382    0.6562   -1.1925 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2674    0.5930   -2.5837 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7137   -0.5005   -3.2600 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1247   -1.5474   -2.5207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9327   -3.3917    0.0751 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7184   -5.0886   -0.8381 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9901   -3.4673   -1.0680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3102   -5.3898    1.2360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2237   -3.1261    1.5379 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2904   -6.3811   -0.6881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0183   -5.5297    0.1882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7830   -5.1467   -4.9096 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4253   -2.9640   -5.0439 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2709   -2.7690    0.3163 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6358   -0.3157    0.6469 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6722    1.5146   -0.6847 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7228    1.4005   -3.1517 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7384   -0.5389   -4.3447 H   0  0  0  0  0  0  0  0  0  0  0  0
 10 18  1  0
 13 18  2  0
 11  6  2  0
 18 17  1  0
 13 12  1  0
 17 16  2  0
  6  7  1  0
 16 15  1  0
 12 11  1  0
 15 14  2  0
 14 13  1  0
  7  8  2  0
  6  5  1  0
  5  3  1  0
  8  9  1  0
  3  2  1  0
  9 10  2  0
  2  1  1  0
 10 11  1  0
  3  4  1  0
 12 28  1  0
  8 26  1  0
  9 27  1  0
 17 32  1  0
 16 31  1  0
 15 30  1  0
 14 29  1  0
  5 24  1  0
  5 25  1  0
  3 22  1  1
  2 20  1  0
  2 21  1  0
  1 19  1  0
  4 23  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₄H₁₄N₂O₂

Average Mass

242.2780 Da

Monoisotopic Mass

242.10553 Da

IUPAC Name

(2R)-3-{9H-pyrido[3,4-b]indol-1-yl}propane-1,2-diol

Traditional Name

(2R)-3-{9H-pyrido[3,4-b]indol-1-yl}propane-1,2-diol

CAS Registry Number

Not Available

SMILES

[H]OC([H])([H])[C@]([H])(O[H])C([H])([H])C1=C2N([H])C3=C(C([H])=C([H])C([H])=C3[H])C2=C([H])C([H])=N1

InChI Identifier

InChI=1S/C14H14N2O2/c17-8-9(18)7-13-14-11(5-6-15-13)10-3-1-2-4-12(10)16-14/h1-6,9,16-18H,7-8H2/t9-/m1/s1

InChI Key

OYZWACRLCWKSSL-SECBINFHSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Ophiocordyceps sinensis	JEOL database	Yang, M. -L., et al, J. Nat. Prod. 74, 1996 (2011)

Chemical Taxonomy

Classification

Not classified

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	1.33	ALOGPS
logP	0.79	ChemAxon
logS	-3	ALOGPS
pKa (Strongest Acidic)	13.4	ChemAxon
pKa (Strongest Basic)	5.38	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	69.14 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	68.27 m³·mol⁻¹	ChemAxon
Polarizability	25.91 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

30786425

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

69429

Good Scents ID

Not Available

References

General References

Yang, M. -L., et al. (2011). Yang, M. -L., et al, J. Nat. Prod. 74, 1996 (2011). J. Nat. Prod..

Showing NP-Card for cordysinin E (NP0036201)

MOL for NP0036201 (cordysinin E)

3D MOL for NP0036201 (cordysinin E)

3D SDF for NP0036201 (cordysinin E)

3D-SDF for NP0036201 (cordysinin E)

PDB for NP0036201 (cordysinin E)

3D PDB for NP0036201 (cordysinin E)

SMILES for NP0036201 (cordysinin E)

INCHI for NP0036201 (cordysinin E)

Structure for NP0036201 (cordysinin E)

3D Structure for NP0036201 (cordysinin E)