NP-MRD: Showing NP-Card for Altemicidin (NP0013955)

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Record Information

Version

2.0

Created at

2021-01-05 23:14:13 UTC

Updated at

2021-07-15 17:15:56 UTC

NP-MRD ID

NP0013955

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Altemicidin

Provided By

NPAtlas

Description

Altemicidin is found in Streptomyces and Streptomyces sioyaensis. Altemicidin was first documented in 1989 (PMID: 2584138). Based on a literature review very few articles have been published on (4aR,6S,7R,7aS)-6-hydroxy-7-[(1-hydroxy-2-sulfamoylethylidene)amino]-4-(C-hydroxycarbonimidoyl)-2-methyl-1H,2H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyridine-7-carboxylic acid.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242119513D          

 45 46  0  0  0  0            999 V2000
   -1.8150   -1.9697    2.6889 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8561   -1.1400    1.4849 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0729   -0.6544    0.9739 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1554    0.1626   -0.0579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4485    0.6255   -0.5392 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6312    0.2121    0.1028 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4885    1.4133   -1.5525 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9353    0.6172   -0.7261 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5217   -0.2738   -1.9049 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0758    0.1828   -2.1331 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6230   -0.8729   -2.6428 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4290    0.7078   -0.8357 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6629    0.0740   -0.4200 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7907    0.1022   -1.2553 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8475    0.6431   -2.3930 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0830   -0.5478   -0.8246 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7412    0.4191    0.5225 S   0  0  1  0  0  6  0  0  0  0  0  0
    6.2182   -0.2569    1.0800 N   0  0  2  0  0  0  0  0  0  0  0  0
    4.9113    1.8275    0.0345 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6951    0.3742    1.6310 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6807    2.1714   -0.9151 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8076    2.6690   -1.1642 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3520    3.1115   -0.7094 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6871    0.4947    0.1360 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6165   -0.8275    0.8298 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3992   -1.3356    3.5106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1397   -2.8309    2.4763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8441   -2.2908    2.9194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0135   -0.9607    1.4505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4003    0.8884    0.2532 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7328   -0.7621    0.4255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0135    1.6246   -1.1525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5815   -1.3120   -1.5427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0890   -0.0880   -2.8111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0617    1.0282   -2.8718 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9689   -1.5217   -1.9854 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7548   -0.4127    0.4871 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7972   -0.6749   -1.6300 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8104   -1.5403   -0.4256 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3322   -1.2303    0.7086 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2134   -0.2211    2.1328 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4909    3.5146    0.2220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7058    1.2786    0.9417 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3981   -1.6696    0.1323 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1588   -0.7486    1.6378 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  2  0  0  0  0
  4  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
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 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
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 17 18  1  1  0  0  0
 17 19  2  0  0  0  0
 17 20  2  0  0  0  0
 12 21  1  6  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 12 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25  2  1  0  0  0  0
 24  8  1  0  0  0  0
  1 26  1  0  0  0  0
  1 27  1  0  0  0  0
  1 28  1  0  0  0  0
  3 29  1  0  0  0  0
  6 30  1  0  0  0  0
  6 31  1  0  0  0  0
  8 32  1  6  0  0  0
  9 33  1  0  0  0  0
  9 34  1  0  0  0  0
 10 35  1  6  0  0  0
 11 36  1  0  0  0  0
 13 37  1  0  0  0  0
 16 38  1  0  0  0  0
 16 39  1  0  0  0  0
 18 40  1  0  0  0  0
 18 41  1  0  0  0  0
 23 42  1  0  0  0  0
 24 43  1  1  0  0  0
 25 44  1  0  0  0  0
 25 45  1  0  0  0  0
M  END

     RDKit          3D

 45 46  0  0  0  0  0  0  0  0999 V2000
   -1.8150   -1.9697    2.6889 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8561   -1.1400    1.4849 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0729   -0.6544    0.9739 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1554    0.1626   -0.0579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4485    0.6255   -0.5392 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6312    0.2121    0.1028 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4885    1.4133   -1.5525 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9353    0.6172   -0.7261 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5217   -0.2738   -1.9049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0758    0.1828   -2.1331 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6230   -0.8729   -2.6428 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4290    0.7078   -0.8357 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6629    0.0740   -0.4200 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7907    0.1022   -1.2553 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8475    0.6431   -2.3930 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0830   -0.5478   -0.8246 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7412    0.4191    0.5225 S   0  0  1  0  0  6  0  0  0  0  0  0
    6.2182   -0.2569    1.0800 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.9113    1.8275    0.0345 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6951    0.3742    1.6310 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6807    2.1714   -0.9151 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8076    2.6690   -1.1642 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3520    3.1115   -0.7094 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6871    0.4947    0.1360 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6165   -0.8275    0.8298 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3992   -1.3356    3.5106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1397   -2.8309    2.4763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8441   -2.2908    2.9194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0135   -0.9607    1.4505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4003    0.8884    0.2532 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7328   -0.7621    0.4255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0135    1.6246   -1.1525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5815   -1.3120   -1.5427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0890   -0.0880   -2.8111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0617    1.0282   -2.8718 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9689   -1.5217   -1.9854 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7548   -0.4127    0.4871 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7972   -0.6749   -1.6300 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8104   -1.5403   -0.4256 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3322   -1.2303    0.7086 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2134   -0.2211    2.1328 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.3981   -1.6696    0.1323 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1588   -0.7486    1.6378 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
  4  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
 17 18  1  1
 17 19  2  0
 17 20  2  0
 12 21  1  6
 21 22  2  0
 21 23  1  0
 12 24  1  0
 24 25  1  0
 25  2  1  0
 24  8  1  0
  1 26  1  0
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 10 35  1  6
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 13 37  1  0
 16 38  1  0
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 18 40  1  0
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 25 45  1  0
M  END


  Mrv1652306242119513D          

 45 46  0  0  0  0            999 V2000
   -1.8150   -1.9697    2.6889 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8561   -1.1400    1.4849 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0729   -0.6544    0.9739 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1554    0.1626   -0.0579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4485    0.6255   -0.5392 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6312    0.2121    0.1028 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4885    1.4133   -1.5525 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9353    0.6172   -0.7261 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5217   -0.2738   -1.9049 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0758    0.1828   -2.1331 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6230   -0.8729   -2.6428 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4290    0.7078   -0.8357 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6629    0.0740   -0.4200 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7907    0.1022   -1.2553 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8475    0.6431   -2.3930 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0830   -0.5478   -0.8246 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7412    0.4191    0.5225 S   0  0  1  0  0  6  0  0  0  0  0  0
    6.2182   -0.2569    1.0800 N   0  0  2  0  0  0  0  0  0  0  0  0
    4.9113    1.8275    0.0345 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6951    0.3742    1.6310 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6807    2.1714   -0.9151 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8076    2.6690   -1.1642 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3520    3.1115   -0.7094 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6871    0.4947    0.1360 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6165   -0.8275    0.8298 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -1.1397   -2.8309    2.4763 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.1588   -0.7486    1.6378 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  2  0  0  0  0
  4  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
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 25  2  1  0  0  0  0
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  1 26  1  0  0  0  0
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  3 29  1  0  0  0  0
  6 30  1  0  0  0  0
  6 31  1  0  0  0  0
  8 32  1  6  0  0  0
  9 33  1  0  0  0  0
  9 34  1  0  0  0  0
 10 35  1  6  0  0  0
 11 36  1  0  0  0  0
 13 37  1  0  0  0  0
 16 38  1  0  0  0  0
 16 39  1  0  0  0  0
 18 40  1  0  0  0  0
 18 41  1  0  0  0  0
 23 42  1  0  0  0  0
 24 43  1  1  0  0  0
 25 44  1  0  0  0  0
 25 45  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0013955

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC(=O)[C@]1(N([H])C(=O)C([H])([H])[S](=O)(=O)N([H])[H])[C@@]([H])(O[H])C([H])([H])[C@@]2([H])C(=C([H])N(C([H])([H])[H])C([H])([H])[C@@]12[H])C(=O)N([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C13H20N4O7S/c1-17-3-7(11(14)20)6-2-9(18)13(12(21)22,8(6)4-17)16-10(19)5-25(15,23)24/h3,6,8-9,18H,2,4-5H2,1H3,(H2,14,20)(H,16,19)(H,21,22)(H2,15,23,24)/t6-,8+,9-,13+/m0/s1

> <INCHI_KEY>
VZRFZUPFQKSXPV-VPFIQFBESA-N

> <FORMULA>
C13H20N4O7S

> <MOLECULAR_WEIGHT>
376.38

> <EXACT_MASS>
376.105270174

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
34.82174750555157

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(4aR,6S,7R,7aS)-4-carbamoyl-6-hydroxy-2-methyl-7-(2-sulfamoylacetamido)-1H,2H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyridine-7-carboxylic acid

> <ALOGPS_LOGP>
-1.50

> <JCHEM_LOGP>
-4.065862399333333

> <ALOGPS_LOGS>
-1.48

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
10.366908860540065

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.3070996809299085

> <JCHEM_PKA_STRONGEST_BASIC>
0.4523804419577974

> <JCHEM_POLAR_SURFACE_AREA>
193.11999999999998

> <JCHEM_REFRACTIVITY>
83.90069999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.24e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4aR,6S,7R,7aS)-4-carbamoyl-6-hydroxy-2-methyl-7-(2-sulfamoylacetamido)-1H,4aH,5H,6H,7aH-cyclopenta[c]pyridine-7-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 45 46  0  0  0  0  0  0  0  0999 V2000
   -1.8150   -1.9697    2.6889 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8561   -1.1400    1.4849 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0729   -0.6544    0.9739 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1554    0.1626   -0.0579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4485    0.6255   -0.5392 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6312    0.2121    0.1028 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4885    1.4133   -1.5525 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9353    0.6172   -0.7261 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5217   -0.2738   -1.9049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0758    0.1828   -2.1331 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6230   -0.8729   -2.6428 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4290    0.7078   -0.8357 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6629    0.0740   -0.4200 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7907    0.1022   -1.2553 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8475    0.6431   -2.3930 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0830   -0.5478   -0.8246 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7412    0.4191    0.5225 S   0  0  1  0  0  6  0  0  0  0  0  0
    6.2182   -0.2569    1.0800 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.9113    1.8275    0.0345 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6951    0.3742    1.6310 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6807    2.1714   -0.9151 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8076    2.6690   -1.1642 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3520    3.1115   -0.7094 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6871    0.4947    0.1360 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6165   -0.8275    0.8298 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3992   -1.3356    3.5106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1397   -2.8309    2.4763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8441   -2.2908    2.9194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0135   -0.9607    1.4505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4003    0.8884    0.2532 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7328   -0.7621    0.4255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0135    1.6246   -1.1525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5815   -1.3120   -1.5427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0890   -0.0880   -2.8111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0617    1.0282   -2.8718 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9689   -1.5217   -1.9854 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7548   -0.4127    0.4871 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7972   -0.6749   -1.6300 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8104   -1.5403   -0.4256 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3322   -1.2303    0.7086 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2134   -0.2211    2.1328 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4909    3.5146    0.2220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7058    1.2786    0.9417 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3981   -1.6696    0.1323 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1588   -0.7486    1.6378 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
  4  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
 17 18  1  1
 17 19  2  0
 17 20  2  0
 12 21  1  6
 21 22  2  0
 21 23  1  0
 12 24  1  0
 24 25  1  0
 25  2  1  0
 24  8  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  3 29  1  0
  6 30  1  0
  6 31  1  0
  8 32  1  6
  9 33  1  0
  9 34  1  0
 10 35  1  6
 11 36  1  0
 13 37  1  0
 16 38  1  0
 16 39  1  0
 18 40  1  0
 18 41  1  0
 23 42  1  0
 24 43  1  1
 25 44  1  0
 25 45  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0      -1.815  -1.970   2.689  0.00  0.00           C+0
HETATM    2  N   UNK     0      -1.856  -1.140   1.485  0.00  0.00           N+0
HETATM    3  C   UNK     0      -3.073  -0.654   0.974  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.155   0.163  -0.058  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.449   0.626  -0.539  0.00  0.00           C+0
HETATM    6  N   UNK     0      -5.631   0.212   0.103  0.00  0.00           N+0
HETATM    7  O   UNK     0      -4.489   1.413  -1.553  0.00  0.00           O+0
HETATM    8  C   UNK     0      -1.935   0.617  -0.726  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.522  -0.274  -1.905  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.076   0.183  -2.133  0.00  0.00           C+0
HETATM   11  O   UNK     0       0.623  -0.873  -2.643  0.00  0.00           O+0
HETATM   12  C   UNK     0       0.429   0.708  -0.836  0.00  0.00           C+0
HETATM   13  N   UNK     0       1.663   0.074  -0.420  0.00  0.00           N+0
HETATM   14  C   UNK     0       2.791   0.102  -1.255  0.00  0.00           C+0
HETATM   15  O   UNK     0       2.848   0.643  -2.393  0.00  0.00           O+0
HETATM   16  C   UNK     0       4.083  -0.548  -0.825  0.00  0.00           C+0
HETATM   17  S   UNK     0       4.741   0.419   0.523  0.00  0.00           S+0
HETATM   18  N   UNK     0       6.218  -0.257   1.080  0.00  0.00           N+0
HETATM   19  O   UNK     0       4.911   1.827   0.035  0.00  0.00           O+0
HETATM   20  O   UNK     0       3.695   0.374   1.631  0.00  0.00           O+0
HETATM   21  C   UNK     0       0.681   2.171  -0.915  0.00  0.00           C+0
HETATM   22  O   UNK     0       1.808   2.669  -1.164  0.00  0.00           O+0
HETATM   23  O   UNK     0      -0.352   3.111  -0.709  0.00  0.00           O+0
HETATM   24  C   UNK     0      -0.687   0.495   0.136  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.617  -0.828   0.830  0.00  0.00           C+0
HETATM   26  H   UNK     0      -1.399  -1.336   3.511  0.00  0.00           H+0
HETATM   27  H   UNK     0      -1.140  -2.831   2.476  0.00  0.00           H+0
HETATM   28  H   UNK     0      -2.844  -2.291   2.919  0.00  0.00           H+0
HETATM   29  H   UNK     0      -4.013  -0.961   1.450  0.00  0.00           H+0
HETATM   30  H   UNK     0      -6.400   0.888   0.253  0.00  0.00           H+0
HETATM   31  H   UNK     0      -5.733  -0.762   0.426  0.00  0.00           H+0
HETATM   32  H   UNK     0      -2.014   1.625  -1.153  0.00  0.00           H+0
HETATM   33  H   UNK     0      -1.581  -1.312  -1.543  0.00  0.00           H+0
HETATM   34  H   UNK     0      -2.089  -0.088  -2.811  0.00  0.00           H+0
HETATM   35  H   UNK     0      -0.062   1.028  -2.872  0.00  0.00           H+0
HETATM   36  H   UNK     0       0.969  -1.522  -1.985  0.00  0.00           H+0
HETATM   37  H   UNK     0       1.755  -0.413   0.487  0.00  0.00           H+0
HETATM   38  H   UNK     0       4.797  -0.675  -1.630  0.00  0.00           H+0
HETATM   39  H   UNK     0       3.810  -1.540  -0.426  0.00  0.00           H+0
HETATM   40  H   UNK     0       6.332  -1.230   0.709  0.00  0.00           H+0
HETATM   41  H   UNK     0       6.213  -0.221   2.133  0.00  0.00           H+0
HETATM   42  H   UNK     0      -0.491   3.515   0.222  0.00  0.00           H+0
HETATM   43  H   UNK     0      -0.706   1.279   0.942  0.00  0.00           H+0
HETATM   44  H   UNK     0      -0.398  -1.670   0.132  0.00  0.00           H+0
HETATM   45  H   UNK     0       0.159  -0.749   1.638  0.00  0.00           H+0
CONECT    1    2   26   27   28                                             
CONECT    2    1    3   25                                                  
CONECT    3    2    4   29                                                  
CONECT    4    3    5    8                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5   30   31                                                  
CONECT    7    5                                                            
CONECT    8    4    9   24   32                                             
CONECT    9    8   10   33   34                                             
CONECT   10    9   11   12   35                                             
CONECT   11   10   36                                                       
CONECT   12   10   13   21   24                                             
CONECT   13   12   14   37                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   38   39                                             
CONECT   17   16   18   19   20                                             
CONECT   18   17   40   41                                                  
CONECT   19   17                                                            
CONECT   20   17                                                            
CONECT   21   12   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   42                                                       
CONECT   24   12   25    8   43                                             
CONECT   25   24    2   44   45                                             
CONECT   26    1                                                            
CONECT   27    1                                                            
CONECT   28    1                                                            
CONECT   29    3                                                            
CONECT   30    6                                                            
CONECT   31    6                                                            
CONECT   32    8                                                            
CONECT   33    9                                                            
CONECT   34    9                                                            
CONECT   35   10                                                            
CONECT   36   11                                                            
CONECT   37   13                                                            
CONECT   38   16                                                            
CONECT   39   16                                                            
CONECT   40   18                                                            
CONECT   41   18                                                            
CONECT   42   23                                                            
CONECT   43   24                                                            
CONECT   44   25                                                            
CONECT   45   25                                                            
MASTER        0    0    0    0    0    0    0    0   45    0   92    0
END

RDKit          3D

45 46  0  0  0  0  0  0  0  0999 V2000
   -1.8150   -1.9697    2.6889 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8561   -1.1400    1.4849 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0729   -0.6544    0.9739 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1554    0.1626   -0.0579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4485    0.6255   -0.5392 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6312    0.2121    0.1028 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4885    1.4133   -1.5525 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9353    0.6172   -0.7261 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5217   -0.2738   -1.9049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0758    0.1828   -2.1331 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6230   -0.8729   -2.6428 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4290    0.7078   -0.8357 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6629    0.0740   -0.4200 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7907    0.1022   -1.2553 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8475    0.6431   -2.3930 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0830   -0.5478   -0.8246 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7412    0.4191    0.5225 S   0  0  1  0  0  6  0  0  0  0  0  0
    6.2182   -0.2569    1.0800 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.9113    1.8275    0.0345 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6951    0.3742    1.6310 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6807    2.1714   -0.9151 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8076    2.6690   -1.1642 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3520    3.1115   -0.7094 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6871    0.4947    0.1360 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6165   -0.8275    0.8298 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3992   -1.3356    3.5106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1397   -2.8309    2.4763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8441   -2.2908    2.9194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0135   -0.9607    1.4505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4003    0.8884    0.2532 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7328   -0.7621    0.4255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0135    1.6246   -1.1525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5815   -1.3120   -1.5427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0890   -0.0880   -2.8111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0617    1.0282   -2.8718 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9689   -1.5217   -1.9854 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7548   -0.4127    0.4871 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7972   -0.6749   -1.6300 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8104   -1.5403   -0.4256 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3322   -1.2303    0.7086 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2134   -0.2211    2.1328 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4909    3.5146    0.2220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7058    1.2786    0.9417 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3981   -1.6696    0.1323 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1588   -0.7486    1.6378 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
  4  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
 17 18  1  1
 17 19  2  0
 17 20  2  0
 12 21  1  6
 21 22  2  0
 21 23  1  0
 12 24  1  0
 24 25  1  0
 25  2  1  0
 24  8  1  0
  1 26  1  0
  1 27  1  0
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  6 31  1  0
  8 32  1  6
  9 33  1  0
  9 34  1  0
 10 35  1  6
 11 36  1  0
 13 37  1  0
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 23 42  1  0
 24 43  1  1
 25 44  1  0
 25 45  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
(4AR,6S,7R,7as)-6-hydroxy-7-[(1-hydroxy-2-sulfamoylethylidene)amino]-4-(C-hydroxycarbonimidoyl)-2-methyl-1H,2H,4ah,5H,6H,7H,7ah-cyclopenta[c]pyridine-7-carboxylate	Generator
(4AR,6S,7R,7as)-6-hydroxy-7-[(1-hydroxy-2-sulphamoylethylidene)amino]-4-(C-hydroxycarbonimidoyl)-2-methyl-1H,2H,4ah,5H,6H,7H,7ah-cyclopenta[c]pyridine-7-carboxylate	Generator
(4AR,6S,7R,7as)-6-hydroxy-7-[(1-hydroxy-2-sulphamoylethylidene)amino]-4-(C-hydroxycarbonimidoyl)-2-methyl-1H,2H,4ah,5H,6H,7H,7ah-cyclopenta[c]pyridine-7-carboxylic acid	Generator

Chemical Formula

C₁₃H₂₀N₄O₇S

Average Mass

376.3800 Da

Monoisotopic Mass

376.10527 Da

IUPAC Name

(4aR,6S,7R,7aS)-4-carbamoyl-6-hydroxy-2-methyl-7-(2-sulfamoylacetamido)-1H,2H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyridine-7-carboxylic acid

Traditional Name

(4aR,6S,7R,7aS)-4-carbamoyl-6-hydroxy-2-methyl-7-(2-sulfamoylacetamido)-1H,4aH,5H,6H,7aH-cyclopenta[c]pyridine-7-carboxylic acid

CAS Registry Number

Not Available

SMILES

CN1C[C@@H]2[C@@H](C[C@H](O)[C@@]2(NC(=O)CS(N)(=O)=O)C(O)=O)C(=C1)C(N)=O

InChI Identifier

InChI=1S/C13H20N4O7S/c1-17-3-7(11(14)20)6-2-9(18)13(12(21)22,8(6)4-17)16-10(19)5-25(15,23)24/h3,6,8-9,18H,2,4-5H2,1H3,(H2,14,20)(H,16,19)(H,21,22)(H2,15,23,24)/t6-,8+,9-,13+/m0/s1

InChI Key

VZRFZUPFQKSXPV-VPFIQFBESA-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
Streptomyces	NPAtlas	2584138
Streptomyces sioyaensis	LOTUS Database	35616633

Species Where Detected

Species Name	Source	Reference
Streptomyces sioyaensis SA-1758	KNApSAcK Database	22123792

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	-1.5	ALOGPS
logP	-4.1	ChemAxon
logS	-1.5	ALOGPS
pKa (Strongest Acidic)	3.31	ChemAxon
pKa (Strongest Basic)	0.45	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	193.12 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	83.9 m³·mol⁻¹	ChemAxon
Polarizability	34.82 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

NPAtlas ID

NPA013044

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

9211348

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11036174

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Takahashi A, Ikeda D, Nakamura H, Naganawa H, Kurasawa S, Okami Y, Takeuchi T, IitakaY: Altemicidin, a new acaricidal and antitumor substance. II. Structure determination. J Antibiot (Tokyo). 1989 Nov;42(11):1562-6. doi: 10.7164/antibiotics.42.1562. [PubMed:2584138 ]

Showing NP-Card for Altemicidin (NP0013955)

MOL for NP0013955 (Altemicidin)

3D MOL for NP0013955 (Altemicidin)

3D SDF for NP0013955 (Altemicidin)

3D-SDF for NP0013955 (Altemicidin)

PDB for NP0013955 (Altemicidin)

3D PDB for NP0013955 (Altemicidin)

SMILES for NP0013955 (Altemicidin)

INCHI for NP0013955 (Altemicidin)

Structure for NP0013955 (Altemicidin)

3D Structure for NP0013955 (Altemicidin)