NP-MRD: Showing NP-Card for tecleabine (NP0030991)

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Record Information

Version

2.0

Created at

2021-06-19 22:12:08 UTC

Updated at

2021-06-29 23:59:18 UTC

NP-MRD ID

NP0030991

Secondary Accession Numbers

None

Natural Product Identification

Common Name

tecleabine

Provided By

JEOL Database JEOL Logo

Description

4,6-Dimethoxy-8-[(3-methylbut-2-en-1-yl)oxy]furo[2,3-b]quinoline belongs to the class of organic compounds known as furanoquinolines. Furanoquinolines are compounds containing a furan ring fused to a quinoline. tecleabine is found in Teclea nobilis. tecleabine was first documented in 2003 (Al-Rehaily, A. J., et al.). Based on a literature review very few articles have been published on 4,6-dimethoxy-8-[(3-methylbut-2-en-1-yl)oxy]furo[2,3-b]quinoline.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202100123D          

 42 44  0  0  0  0            999 V2000
    6.6313    3.1849    1.0340 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5605    2.9603    1.9437 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7536    1.8874    1.6942 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8875    0.9816    0.6553 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9743   -0.0779    0.5026 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2872   -0.8583   -0.5918 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2291   -1.5973   -1.2073 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7185   -1.9877   -2.5752 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1323   -1.7843   -3.7723 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8021   -2.2495   -5.0394 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8077   -1.1069   -3.9901 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9181   -0.2850    1.4101 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0802   -1.3278    1.2643 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0902   -1.4233    2.1592 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1431   -2.4025    2.1160 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7053   -2.1857    3.1546 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3159   -1.0800    3.8739 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8526   -0.5867    3.2370 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7568    0.4654    3.4178 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5926    1.3648    4.4514 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1313    0.8256    5.6601 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7955    0.6434    2.4768 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7064    1.7155    2.5923 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1689    4.0787    1.3651 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2570    3.3764    0.0229 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3380    2.3485    1.0431 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6875    1.0668   -0.0739 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0496   -2.5196   -0.6448 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3192   -0.9951   -1.2619 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6790   -2.5015   -2.5515 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9842   -1.3996   -5.7054 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1657   -2.9714   -5.5617 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7656   -2.7336   -4.8481 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1312   -1.7732   -4.5360 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3016   -0.8251   -3.0650 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9451   -0.1962   -4.5824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5211   -2.8899    3.2436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8101   -0.6758    4.7458 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1772    0.5240    5.5339 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5326   -0.0184    6.0173 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0953    1.6111    6.4208 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6023    2.4340    3.4043 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  1  0  0  0  0
 12  5  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
  4  3  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 22 19  1  0  0  0  0
  3  2  1  0  0  0  0
 12 13  1  0  0  0  0
  2  1  1  0  0  0  0
 13 14  2  0  0  0  0
  5  6  1  0  0  0  0
 18 19  2  0  0  0  0
  6  7  1  0  0  0  0
 18 14  1  0  0  0  0
  3 23  1  0  0  0  0
  8  9  2  3  0  0  0
  7  8  1  0  0  0  0
 23 22  2  0  0  0  0
  9 10  1  0  0  0  0
 22 12  1  0  0  0  0
  9 11  1  0  0  0  0
  4 27  1  0  0  0  0
 23 42  1  0  0  0  0
 16 37  1  0  0  0  0
 17 38  1  0  0  0  0
 21 39  1  0  0  0  0
 21 40  1  0  0  0  0
 21 41  1  0  0  0  0
  1 24  1  0  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
  7 28  1  0  0  0  0
  7 29  1  0  0  0  0
  8 30  1  0  0  0  0
 10 31  1  0  0  0  0
 10 32  1  0  0  0  0
 10 33  1  0  0  0  0
 11 34  1  0  0  0  0
 11 35  1  0  0  0  0
 11 36  1  0  0  0  0
M  END

     RDKit          3D

 42 44  0  0  0  0  0  0  0  0999 V2000
    6.6313    3.1849    1.0340 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5605    2.9603    1.9437 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7536    1.8874    1.6942 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8875    0.9816    0.6553 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9743   -0.0779    0.5026 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2872   -0.8583   -0.5918 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2291   -1.5973   -1.2073 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7185   -1.9877   -2.5752 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1323   -1.7843   -3.7723 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8021   -2.2495   -5.0394 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8077   -1.1069   -3.9901 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9181   -0.2850    1.4101 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0802   -1.3278    1.2643 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0902   -1.4233    2.1592 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1431   -2.4025    2.1160 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7053   -2.1857    3.1546 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3159   -1.0800    3.8739 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8526   -0.5867    3.2370 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7568    0.4654    3.4178 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5926    1.3648    4.4514 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1313    0.8256    5.6601 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7955    0.6434    2.4768 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7064    1.7155    2.5923 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1689    4.0787    1.3651 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2570    3.3764    0.0229 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3380    2.3485    1.0431 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6875    1.0668   -0.0739 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0496   -2.5196   -0.6448 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3192   -0.9951   -1.2619 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6790   -2.5015   -2.5515 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9842   -1.3996   -5.7054 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1657   -2.9714   -5.5617 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7656   -2.7336   -4.8481 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1312   -1.7732   -4.5360 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3016   -0.8251   -3.0650 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9451   -0.1962   -4.5824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5211   -2.8899    3.2436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8101   -0.6758    4.7458 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1772    0.5240    5.5339 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5326   -0.0184    6.0173 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0953    1.6111    6.4208 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6023    2.4340    3.4043 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  1  0
 12  5  2  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
  4  3  2  0
 19 20  1  0
 20 21  1  0
 22 19  1  0
  3  2  1  0
 12 13  1  0
  2  1  1  0
 13 14  2  0
  5  6  1  0
 18 19  2  0
  6  7  1  0
 18 14  1  0
  3 23  1  0
  8  9  2  3
  7  8  1  0
 23 22  2  0
  9 10  1  0
 22 12  1  0
  9 11  1  0
  4 27  1  0
 23 42  1  0
 16 37  1  0
 17 38  1  0
 21 39  1  0
 21 40  1  0
 21 41  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  7 28  1  0
  7 29  1  0
  8 30  1  0
 10 31  1  0
 10 32  1  0
 10 33  1  0
 11 34  1  0
 11 35  1  0
 11 36  1  0
M  END


  Mrv1652306202100123D          

 42 44  0  0  0  0            999 V2000
    6.6313    3.1849    1.0340 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5605    2.9603    1.9437 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7536    1.8874    1.6942 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8875    0.9816    0.6553 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9743   -0.0779    0.5026 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2872   -0.8583   -0.5918 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2291   -1.5973   -1.2073 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7185   -1.9877   -2.5752 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1323   -1.7843   -3.7723 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8021   -2.2495   -5.0394 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8077   -1.1069   -3.9901 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9181   -0.2850    1.4101 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0802   -1.3278    1.2643 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0902   -1.4233    2.1592 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1431   -2.4025    2.1160 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7053   -2.1857    3.1546 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3159   -1.0800    3.8739 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8526   -0.5867    3.2370 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7568    0.4654    3.4178 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5926    1.3648    4.4514 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1313    0.8256    5.6601 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7955    0.6434    2.4768 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7064    1.7155    2.5923 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1689    4.0787    1.3651 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2570    3.3764    0.0229 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3380    2.3485    1.0431 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6875    1.0668   -0.0739 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0496   -2.5196   -0.6448 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3192   -0.9951   -1.2619 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6790   -2.5015   -2.5515 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9842   -1.3996   -5.7054 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1657   -2.9714   -5.5617 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7656   -2.7336   -4.8481 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1312   -1.7732   -4.5360 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3016   -0.8251   -3.0650 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9451   -0.1962   -4.5824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5211   -2.8899    3.2436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8101   -0.6758    4.7458 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1772    0.5240    5.5339 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5326   -0.0184    6.0173 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0953    1.6111    6.4208 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6023    2.4340    3.4043 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  1  0  0  0  0
 12  5  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
  4  3  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 22 19  1  0  0  0  0
  3  2  1  0  0  0  0
 12 13  1  0  0  0  0
  2  1  1  0  0  0  0
 13 14  2  0  0  0  0
  5  6  1  0  0  0  0
 18 19  2  0  0  0  0
  6  7  1  0  0  0  0
 18 14  1  0  0  0  0
  3 23  1  0  0  0  0
  8  9  2  3  0  0  0
  7  8  1  0  0  0  0
 23 22  2  0  0  0  0
  9 10  1  0  0  0  0
 22 12  1  0  0  0  0
  9 11  1  0  0  0  0
  4 27  1  0  0  0  0
 23 42  1  0  0  0  0
 16 37  1  0  0  0  0
 17 38  1  0  0  0  0
 21 39  1  0  0  0  0
 21 40  1  0  0  0  0
 21 41  1  0  0  0  0
  1 24  1  0  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
  7 28  1  0  0  0  0
  7 29  1  0  0  0  0
  8 30  1  0  0  0  0
 10 31  1  0  0  0  0
 10 32  1  0  0  0  0
 10 33  1  0  0  0  0
 11 34  1  0  0  0  0
 11 35  1  0  0  0  0
 11 36  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0030991

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]C(=C(C([H])([H])[H])C([H])([H])[H])C([H])([H])OC1=C2N=C3OC([H])=C([H])C3=C(OC([H])([H])[H])C2=C([H])C(OC([H])([H])[H])=C1[H]

> <INCHI_IDENTIFIER>
InChI=1S/C18H19NO4/c1-11(2)5-7-22-15-10-12(20-3)9-14-16(15)19-18-13(6-8-23-18)17(14)21-4/h5-6,8-10H,7H2,1-4H3

> <INCHI_KEY>
YAAZBRKEIHCVOT-UHFFFAOYSA-N

> <FORMULA>
C18H19NO4

> <MOLECULAR_WEIGHT>
313.353

> <EXACT_MASS>
313.131408096

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
34.69861253273166

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4,6-dimethoxy-8-[(3-methylbut-2-en-1-yl)oxy]furo[2,3-b]quinoline

> <ALOGPS_LOGP>
3.86

> <JCHEM_LOGP>
3.545718219666666

> <ALOGPS_LOGS>
-3.71

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
1.6065339296768102

> <JCHEM_POLAR_SURFACE_AREA>
53.72

> <JCHEM_REFRACTIVITY>
87.2808

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.11e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4,6-dimethoxy-8-[(3-methylbut-2-en-1-yl)oxy]furo[2,3-b]quinoline

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 42 44  0  0  0  0  0  0  0  0999 V2000
    6.6313    3.1849    1.0340 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5605    2.9603    1.9437 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7536    1.8874    1.6942 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8875    0.9816    0.6553 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9743   -0.0779    0.5026 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2872   -0.8583   -0.5918 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2291   -1.5973   -1.2073 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7185   -1.9877   -2.5752 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1323   -1.7843   -3.7723 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8021   -2.2495   -5.0394 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8077   -1.1069   -3.9901 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9181   -0.2850    1.4101 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0802   -1.3278    1.2643 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0902   -1.4233    2.1592 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1431   -2.4025    2.1160 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7053   -2.1857    3.1546 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3159   -1.0800    3.8739 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8526   -0.5867    3.2370 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7568    0.4654    3.4178 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5926    1.3648    4.4514 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1313    0.8256    5.6601 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7955    0.6434    2.4768 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7064    1.7155    2.5923 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1689    4.0787    1.3651 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2570    3.3764    0.0229 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3380    2.3485    1.0431 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6875    1.0668   -0.0739 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0496   -2.5196   -0.6448 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3192   -0.9951   -1.2619 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6790   -2.5015   -2.5515 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9842   -1.3996   -5.7054 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1657   -2.9714   -5.5617 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7656   -2.7336   -4.8481 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1312   -1.7732   -4.5360 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3016   -0.8251   -3.0650 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9451   -0.1962   -4.5824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5211   -2.8899    3.2436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8101   -0.6758    4.7458 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1772    0.5240    5.5339 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5326   -0.0184    6.0173 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0953    1.6111    6.4208 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6023    2.4340    3.4043 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  1  0
 12  5  2  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
  4  3  2  0
 19 20  1  0
 20 21  1  0
 22 19  1  0
  3  2  1  0
 12 13  1  0
  2  1  1  0
 13 14  2  0
  5  6  1  0
 18 19  2  0
  6  7  1  0
 18 14  1  0
  3 23  1  0
  8  9  2  3
  7  8  1  0
 23 22  2  0
  9 10  1  0
 22 12  1  0
  9 11  1  0
  4 27  1  0
 23 42  1  0
 16 37  1  0
 17 38  1  0
 21 39  1  0
 21 40  1  0
 21 41  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  7 28  1  0
  7 29  1  0
  8 30  1  0
 10 31  1  0
 10 32  1  0
 10 33  1  0
 11 34  1  0
 11 35  1  0
 11 36  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  C   UNK     0       6.631   3.185   1.034  0.00  0.00           C+0
HETATM    2  O   UNK     0       5.561   2.960   1.944  0.00  0.00           O+0
HETATM    3  C   UNK     0       4.754   1.887   1.694  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.888   0.982   0.655  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.974  -0.078   0.503  0.00  0.00           C+0
HETATM    6  O   UNK     0       4.287  -0.858  -0.592  0.00  0.00           O+0
HETATM    7  C   UNK     0       3.229  -1.597  -1.207  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.719  -1.988  -2.575  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.132  -1.784  -3.772  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.802  -2.249  -5.039  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.808  -1.107  -3.990  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.918  -0.285   1.410  0.00  0.00           C+0
HETATM   13  N   UNK     0       2.080  -1.328   1.264  0.00  0.00           N+0
HETATM   14  C   UNK     0       1.090  -1.423   2.159  0.00  0.00           C+0
HETATM   15  O   UNK     0       0.143  -2.402   2.116  0.00  0.00           O+0
HETATM   16  C   UNK     0      -0.705  -2.186   3.155  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.316  -1.080   3.874  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.853  -0.587   3.237  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.757   0.465   3.418  0.00  0.00           C+0
HETATM   20  O   UNK     0       1.593   1.365   4.451  0.00  0.00           O+0
HETATM   21  C   UNK     0       2.131   0.826   5.660  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.796   0.643   2.477  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.706   1.716   2.592  0.00  0.00           C+0
HETATM   24  H   UNK     0       7.169   4.079   1.365  0.00  0.00           H+0
HETATM   25  H   UNK     0       6.257   3.376   0.023  0.00  0.00           H+0
HETATM   26  H   UNK     0       7.338   2.349   1.043  0.00  0.00           H+0
HETATM   27  H   UNK     0       5.688   1.067  -0.074  0.00  0.00           H+0
HETATM   28  H   UNK     0       3.050  -2.520  -0.645  0.00  0.00           H+0
HETATM   29  H   UNK     0       2.319  -0.995  -1.262  0.00  0.00           H+0
HETATM   30  H   UNK     0       4.679  -2.502  -2.551  0.00  0.00           H+0
HETATM   31  H   UNK     0       3.984  -1.400  -5.705  0.00  0.00           H+0
HETATM   32  H   UNK     0       3.166  -2.971  -5.562  0.00  0.00           H+0
HETATM   33  H   UNK     0       4.766  -2.734  -4.848  0.00  0.00           H+0
HETATM   34  H   UNK     0       1.131  -1.773  -4.536  0.00  0.00           H+0
HETATM   35  H   UNK     0       1.302  -0.825  -3.065  0.00  0.00           H+0
HETATM   36  H   UNK     0       1.945  -0.196  -4.582  0.00  0.00           H+0
HETATM   37  H   UNK     0      -1.521  -2.890   3.244  0.00  0.00           H+0
HETATM   38  H   UNK     0      -0.810  -0.676   4.746  0.00  0.00           H+0
HETATM   39  H   UNK     0       3.177   0.524   5.534  0.00  0.00           H+0
HETATM   40  H   UNK     0       1.533  -0.018   6.017  0.00  0.00           H+0
HETATM   41  H   UNK     0       2.095   1.611   6.421  0.00  0.00           H+0
HETATM   42  H   UNK     0       3.602   2.434   3.404  0.00  0.00           H+0
CONECT    1    2   24   25   26                                             
CONECT    2    3    1                                                       
CONECT    3    4    2   23                                                  
CONECT    4    5    3   27                                                  
CONECT    5    4   12    6                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   28   29                                             
CONECT    8    9    7   30                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9   31   32   33                                             
CONECT   11    9   34   35   36                                             
CONECT   12    5   13   22                                                  
CONECT   13   12   14                                                       
CONECT   14   15   13   18                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   37                                                  
CONECT   17   16   18   38                                                  
CONECT   18   17   19   14                                                  
CONECT   19   20   22   18                                                  
CONECT   20   19   21                                                       
CONECT   21   20   39   40   41                                             
CONECT   22   19   23   12                                                  
CONECT   23    3   22   42                                                  
CONECT   24    1                                                            
CONECT   25    1                                                            
CONECT   26    1                                                            
CONECT   27    4                                                            
CONECT   28    7                                                            
CONECT   29    7                                                            
CONECT   30    8                                                            
CONECT   31   10                                                            
CONECT   32   10                                                            
CONECT   33   10                                                            
CONECT   34   11                                                            
CONECT   35   11                                                            
CONECT   36   11                                                            
CONECT   37   16                                                            
CONECT   38   17                                                            
CONECT   39   21                                                            
CONECT   40   21                                                            
CONECT   41   21                                                            
CONECT   42   23                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   88    0
END

RDKit          3D

42 44  0  0  0  0  0  0  0  0999 V2000
    6.6313    3.1849    1.0340 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5605    2.9603    1.9437 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7536    1.8874    1.6942 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8875    0.9816    0.6553 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9743   -0.0779    0.5026 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2872   -0.8583   -0.5918 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2291   -1.5973   -1.2073 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7185   -1.9877   -2.5752 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1323   -1.7843   -3.7723 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8021   -2.2495   -5.0394 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8077   -1.1069   -3.9901 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9181   -0.2850    1.4101 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0802   -1.3278    1.2643 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0902   -1.4233    2.1592 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1431   -2.4025    2.1160 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7053   -2.1857    3.1546 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3159   -1.0800    3.8739 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8526   -0.5867    3.2370 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7568    0.4654    3.4178 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5926    1.3648    4.4514 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1313    0.8256    5.6601 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7955    0.6434    2.4768 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7064    1.7155    2.5923 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1689    4.0787    1.3651 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2570    3.3764    0.0229 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3380    2.3485    1.0431 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6875    1.0668   -0.0739 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0496   -2.5196   -0.6448 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3192   -0.9951   -1.2619 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6790   -2.5015   -2.5515 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9842   -1.3996   -5.7054 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1657   -2.9714   -5.5617 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7656   -2.7336   -4.8481 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1312   -1.7732   -4.5360 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3016   -0.8251   -3.0650 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9451   -0.1962   -4.5824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5211   -2.8899    3.2436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8101   -0.6758    4.7458 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1772    0.5240    5.5339 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5326   -0.0184    6.0173 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0953    1.6111    6.4208 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6023    2.4340    3.4043 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  1  0
 12  5  2  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
  4  3  2  0
 19 20  1  0
 20 21  1  0
 22 19  1  0
  3  2  1  0
 12 13  1  0
  2  1  1  0
 13 14  2  0
  5  6  1  0
 18 19  2  0
  6  7  1  0
 18 14  1  0
  3 23  1  0
  8  9  2  3
  7  8  1  0
 23 22  2  0
  9 10  1  0
 22 12  1  0
  9 11  1  0
  4 27  1  0
 23 42  1  0
 16 37  1  0
 17 38  1  0
 21 39  1  0
 21 40  1  0
 21 41  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  7 28  1  0
  7 29  1  0
  8 30  1  0
 10 31  1  0
 10 32  1  0
 10 33  1  0
 11 34  1  0
 11 35  1  0
 11 36  1  0
M  END

View in JSmol View DFT Assignments 3D Conformers

Synonyms

Not Available

Chemical Formula

C₁₈H₁₉NO₄

Average Mass

313.3530 Da

Monoisotopic Mass

313.13141 Da

IUPAC Name

4,6-dimethoxy-8-[(3-methylbut-2-en-1-yl)oxy]furo[2,3-b]quinoline

Traditional Name

4,6-dimethoxy-8-[(3-methylbut-2-en-1-yl)oxy]furo[2,3-b]quinoline

CAS Registry Number

Not Available

SMILES

[H]C(=C(C([H])([H])[H])C([H])([H])[H])C([H])([H])OC1=C2N=C3OC([H])=C([H])C3=C(OC([H])([H])[H])C2=C([H])C(OC([H])([H])[H])=C1[H]

InChI Identifier

InChI=1S/C18H19NO4/c1-11(2)5-7-22-15-10-12(20-3)9-14-16(15)19-18-13(6-8-23-18)17(14)21-4/h5-6,8-10H,7H2,1-4H3

InChI Key

YAAZBRKEIHCVOT-UHFFFAOYSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 125 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 175 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 225 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 250 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, chcl3, 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
Teclea nobilis	KNApSAcK Database	22123792
Vepris nobilis	JEOL database	Al-Rehaily, A. J., et al, Phytochemistry 64, 1405 (2003)

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as furanoquinolines. Furanoquinolines are compounds containing a furan ring fused to a quinoline.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolines and derivatives

Sub Class

Furanoquinolines

Direct Parent

Furanoquinolines

Alternative Parents

Substituents

Furanoquinoline
Furopyridine
Anisole
Alkyl aryl ether
Pyridine
Benzenoid
Furan
Heteroaromatic compound
Oxacycle
Azacycle
Ether
Organic oxygen compound
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Hydrocarbon derivative
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	3.86	ALOGPS
logP	3.55	ChemAxon
logS	-3.7	ALOGPS
pKa (Strongest Basic)	1.61	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	53.72 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	87.28 m³·mol⁻¹	ChemAxon
Polarizability	34.7 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

C00036225

Chemspider ID

557003

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

Not Available

Good Scents ID

Not Available

References

General References

Al-Rehaily, A. J., et al. (2003). Al-Rehaily, A. J., et al, Phytochemistry 64, 1405 (2003) . Phytochem..

Showing NP-Card for tecleabine (NP0030991)

MOL for NP0030991 (tecleabine)

3D MOL for NP0030991 (tecleabine)

3D SDF for NP0030991 (tecleabine)

3D-SDF for NP0030991 (tecleabine)

PDB for NP0030991 (tecleabine)

3D PDB for NP0030991 (tecleabine)

SMILES for NP0030991 (tecleabine)

INCHI for NP0030991 (tecleabine)

Structure for NP0030991 (tecleabine)

3D Structure for NP0030991 (tecleabine)