NP-MRD: Showing NP-Card for (2r,11s,13r)-22-chloro-2,5,28-trihydroxy-21-methoxy-7-methyl-14,16,19-trioxa-6-azaheptacyclo[15.11.1.0²,¹¹.0⁴,⁹.0¹³,²⁹.0¹⁸,²⁷.0²⁰,²⁵]nonacosa-1(29),4,6,8,17,20,22,24,27-nonaene-3,10,26-trione (NP0157947)

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Record Information

Version

1.0

Created at

2022-09-02 15:27:10 UTC

Updated at

2022-09-02 15:27:10 UTC

NP-MRD ID

NP0157947

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,11s,13r)-22-chloro-2,5,28-trihydroxy-21-methoxy-7-methyl-14,16,19-trioxa-6-azaheptacyclo[15.11.1.0²,¹¹.0⁴,⁹.0¹³,²⁹.0¹⁸,²⁷.0²⁰,²⁵]nonacosa-1(29),4,6,8,17,20,22,24,27-nonaene-3,10,26-trione

Description

Xantholipin belongs to the class of organic compounds known as xanthones. These are polycyclic aromatic compounds containing a xanthene moiety conjugated to a ketone group at carbon 9. Xanthene is a tricyclic compound made up of two benzene rings linearly fused to each other through a pyran ring. It was first documented in 2020 (PMID: 32651204). Based on a literature review a significant number of articles have been published on Xantholipin (PMID: 35512262) (PMID: 34962769) (PMID: 34564766) (PMID: 32649177).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022217272D          

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M  END

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  Mrv1652309022217272D          

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 36 37  2  0  0  0  0
 36 38  1  0  0  0  0
 14 38  1  0  0  0  0
 25 38  1  0  0  0  0
 38 39  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0157947

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C2OC3=C4OCO[C@@H]5C[C@@H]6C(=O)C7=CC(C)=NC(O)=C7C(=O)[C@]6(O)C(C(O)=C3C(=O)C2=CC=C1Cl)=C45

> <INCHI_IDENTIFIER>
InChI=1S/C27H18ClNO10/c1-8-5-10-14(26(34)29-8)25(33)27(35)11(18(10)30)6-13-15-17(27)20(32)16-19(31)9-3-4-12(28)22(36-2)21(9)39-24(16)23(15)38-7-37-13/h3-5,11,13,32,35H,6-7H2,1-2H3,(H,29,34)/t11-,13-,27-/m1/s1

> <INCHI_KEY>
HSVRTPZWHMWONP-JUEDDRGBSA-N

> <FORMULA>
C27H18ClNO10

> <MOLECULAR_WEIGHT>
551.89

> <EXACT_MASS>
551.0619235

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
51.48063390894022

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,11S,13R)-22-chloro-2,5,28-trihydroxy-21-methoxy-7-methyl-14,16,19-trioxa-6-azaheptacyclo[15.11.1.0^{2,11}.0^{4,9}.0^{13,29}.0^{18,27}.0^{20,25}]nonacosa-1(29),4(9),5,7,17,20(25),21,23,27-nonaene-3,10,26-trione

> <ALOGPS_LOGP>
2.94

> <JCHEM_LOGP>
3.641716281333334

> <ALOGPS_LOGS>
-3.41

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.844604448944661

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.758002520395808

> <JCHEM_PKA_STRONGEST_BASIC>
0.2581505813775058

> <JCHEM_POLAR_SURFACE_AREA>
161.70999999999998

> <JCHEM_REFRACTIVITY>
133.14879999999994

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.13e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,11S,13R)-22-chloro-2,5,28-trihydroxy-21-methoxy-7-methyl-14,16,19-trioxa-6-azaheptacyclo[15.11.1.0^{2,11}.0^{4,9}.0^{13,29}.0^{18,27}.0^{20,25}]nonacosa-1(29),4(9),5,7,17,20(25),21,23,27-nonaene-3,10,26-trione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0      -8.088   1.463   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -6.559   1.286   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -5.947  -0.127   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -6.865  -1.363   0.000  0.00  0.00           C+0
HETATM    5 Cl   UNK     0      -8.394  -1.187   0.000  0.00  0.00          Cl+0
HETATM    6  C   UNK     0      -6.253  -2.777   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -4.723  -2.953   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -3.805  -1.717   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.275  -1.893   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -1.663  -3.307   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -1.357  -0.657   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.173  -0.833   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       0.785  -2.247   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       1.091   0.403   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.479   1.816   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.051   1.993   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.969   0.756   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -3.499   0.933   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -4.417  -0.303   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -1.663   3.406   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -0.745   4.643   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       0.785   4.466   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       1.397   3.053   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.926   2.876   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.538   1.463   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.068   1.286   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       5.986   2.523   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       5.680  -0.127   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       7.210  -0.303   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       7.822  -1.717   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       9.352  -1.893   0.000  0.00  0.00           C+0
HETATM   32  N   UNK     0       6.904  -2.953   0.000  0.00  0.00           N+0
HETATM   33  C   UNK     0       5.374  -2.777   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       4.456  -4.013   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       4.762  -1.363   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       3.232  -1.187   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       2.314  -2.423   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       2.620   0.227   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       1.703  -1.010   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   19                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   19                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   17                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   38                                                  
CONECT   15   14   16   23                                                  
CONECT   16   15   17   20                                                  
CONECT   17   16   11   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18    3    8                                                  
CONECT   20   16   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   15   24                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   38                                                  
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   35                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   28   36                                                  
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   14   25   39                                             
CONECT   39   38                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   90    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₇H₁₈ClNO₁₀

Average Mass

551.8900 Da

Monoisotopic Mass

551.06192 Da

IUPAC Name

(2R,11S,13R)-22-chloro-2,5,28-trihydroxy-21-methoxy-7-methyl-14,16,19-trioxa-6-azaheptacyclo[15.11.1.0^{2,11}.0^{4,9}.0^{13,29}.0^{18,27}.0^{20,25}]nonacosa-1(29),4(9),5,7,17,20(25),21,23,27-nonaene-3,10,26-trione

Traditional Name

CAS Registry Number

Not Available

SMILES

COC1=C2OC3=C4OCO[C@@H]5C[C@@H]6C(=O)C7=CC(C)=NC(O)=C7C(=O)[C@]6(O)C(C(O)=C3C(=O)C2=CC=C1Cl)=C45

InChI Identifier

InChI=1S/C27H18ClNO10/c1-8-5-10-14(26(34)29-8)25(33)27(35)11(18(10)30)6-13-15-17(27)20(32)16-19(31)9-3-4-12(28)22(36-2)21(9)39-24(16)23(15)38-7-37-13/h3-5,11,13,32,35H,6-7H2,1-2H3,(H,29,34)/t11-,13-,27-/m1/s1

InChI Key

HSVRTPZWHMWONP-JUEDDRGBSA-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, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as xanthones. These are polycyclic aromatic compounds containing a xanthene moiety conjugated to a ketone group at carbon 9. Xanthene is a tricyclic compound made up of two benzene rings linearly fused to each other through a pyran ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

Xanthones

Alternative Parents

Substituents

Xanthone
Naphthopyranone
Phenanthrene
Naphthopyran
Chromone
Isoquinolone
Naphthalene
Tetralin
Anisole
Aryl alkyl ketone
Aryl ketone
Methylpyridine
Alkyl aryl ether
Pyranone
Pyridinone
Pyridine
Pyran
Benzenoid
Aryl halide
Aryl chloride
Heteroaromatic compound
Vinylogous amide
Vinylogous acid
Tertiary alcohol
Ketone
Lactam
Ether
Acetal
Oxacycle
Azacycle
Organochloride
Organic nitrogen compound
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organohalogen compound
Organooxygen compound
Organonitrogen compound
Alcohol
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	2.94	ALOGPS
logP	3.64	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	8.76	ChemAxon
pKa (Strongest Basic)	0.26	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	161.71 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	133.15 m³·mol⁻¹	ChemAxon
Polarizability	51.48 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

9181348

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11006158

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Leetanasaksakul K, Koomsiri W, Suga T, Matsuo H, Hokari R, Wattana-Amorn P, Takahashi YK, Shiomi K, Nakashima T, Inahashi Y, Thamchaipenet A: Sattahipmycin, a Hexacyclic Xanthone Produced by a Marine-Derived Streptomyces. J Nat Prod. 2022 May 27;85(5):1211-1217. doi: 10.1021/acs.jnatprod.1c00870. Epub 2022 May 5. [PubMed:35512262 ]
Toplak M, Teufel R: Three Rings to Rule Them All: How Versatile Flavoenzymes Orchestrate the Structural Diversification of Natural Products. Biochemistry. 2022 Jan 18;61(2):47-56. doi: 10.1021/acs.biochem.1c00763. Epub 2021 Dec 28. [PubMed:34962769 ]
Vela Gurovic MS, Diaz ML, Gallo CA, Dietrich J: Phylogenomics, CAZyome and core secondary metabolome of Streptomyces albus species. Mol Genet Genomics. 2021 Nov;296(6):1299-1311. doi: 10.1007/s00438-021-01823-9. Epub 2021 Sep 26. [PubMed:34564766 ]
Kong L, Wang Q, Deng Z, You D: Flavin Adenine Dinucleotide-Dependent Halogenase XanH and Engineering of Multifunctional Fusion Halogenases. Appl Environ Microbiol. 2020 Sep 1;86(18):e01225-20. doi: 10.1128/AEM.01225-20. Print 2020 Sep 1. [PubMed:32651204 ]
Kong L, Wang Q, Yang W, Shen J, Li Y, Zheng X, Wang L, Chu Y, Deng Z, Chooi YH, You D: Three Recently Diverging Duplicated Methyltransferases Exhibit Substrate-Dependent Regioselectivity Essential for Xantholipin Biosynthesis. ACS Chem Biol. 2020 Aug 21;15(8):2107-2115. doi: 10.1021/acschembio.0c00296. Epub 2020 Jul 23. [PubMed:32649177 ]
LOTUS database [Link]

Showing NP-Card for (2r,11s,13r)-22-chloro-2,5,28-trihydroxy-21-methoxy-7-methyl-14,16,19-trioxa-6-azaheptacyclo[15.11.1.0²,¹¹.0⁴,⁹.0¹³,²⁹.0¹⁸,²⁷.0²⁰,²⁵]nonacosa-1(29),4,6,8,17,20,22,24,27-nonaene-3,10,26-trione (NP0157947)

MOL for NP0157947 ((2r,11s,13r)-22-chloro-2,5,28-trihydroxy-21-methoxy-7-methyl-14,16,19-trioxa-6-azaheptacyclo[15.11.1.0²,¹¹.0⁴,⁹.0¹³,²⁹.0¹⁸,²⁷.0²⁰,²⁵]nonacosa-1(29),4,6,8,17,20,22,24,27-nonaene-3,10,26-trione)

3D MOL for NP0157947 ((2r,11s,13r)-22-chloro-2,5,28-trihydroxy-21-methoxy-7-methyl-14,16,19-trioxa-6-azaheptacyclo[15.11.1.0²,¹¹.0⁴,⁹.0¹³,²⁹.0¹⁸,²⁷.0²⁰,²⁵]nonacosa-1(29),4,6,8,17,20,22,24,27-nonaene-3,10,26-trione)

3D SDF for NP0157947 ((2r,11s,13r)-22-chloro-2,5,28-trihydroxy-21-methoxy-7-methyl-14,16,19-trioxa-6-azaheptacyclo[15.11.1.0²,¹¹.0⁴,⁹.0¹³,²⁹.0¹⁸,²⁷.0²⁰,²⁵]nonacosa-1(29),4,6,8,17,20,22,24,27-nonaene-3,10,26-trione)

3D-SDF for NP0157947 ((2r,11s,13r)-22-chloro-2,5,28-trihydroxy-21-methoxy-7-methyl-14,16,19-trioxa-6-azaheptacyclo[15.11.1.0²,¹¹.0⁴,⁹.0¹³,²⁹.0¹⁸,²⁷.0²⁰,²⁵]nonacosa-1(29),4,6,8,17,20,22,24,27-nonaene-3,10,26-trione)

PDB for NP0157947 ((2r,11s,13r)-22-chloro-2,5,28-trihydroxy-21-methoxy-7-methyl-14,16,19-trioxa-6-azaheptacyclo[15.11.1.0²,¹¹.0⁴,⁹.0¹³,²⁹.0¹⁸,²⁷.0²⁰,²⁵]nonacosa-1(29),4,6,8,17,20,22,24,27-nonaene-3,10,26-trione)

3D PDB for NP0157947 ((2r,11s,13r)-22-chloro-2,5,28-trihydroxy-21-methoxy-7-methyl-14,16,19-trioxa-6-azaheptacyclo[15.11.1.0²,¹¹.0⁴,⁹.0¹³,²⁹.0¹⁸,²⁷.0²⁰,²⁵]nonacosa-1(29),4,6,8,17,20,22,24,27-nonaene-3,10,26-trione)

SMILES for NP0157947 ((2r,11s,13r)-22-chloro-2,5,28-trihydroxy-21-methoxy-7-methyl-14,16,19-trioxa-6-azaheptacyclo[15.11.1.0²,¹¹.0⁴,⁹.0¹³,²⁹.0¹⁸,²⁷.0²⁰,²⁵]nonacosa-1(29),4,6,8,17,20,22,24,27-nonaene-3,10,26-trione)

INCHI for NP0157947 ((2r,11s,13r)-22-chloro-2,5,28-trihydroxy-21-methoxy-7-methyl-14,16,19-trioxa-6-azaheptacyclo[15.11.1.0²,¹¹.0⁴,⁹.0¹³,²⁹.0¹⁸,²⁷.0²⁰,²⁵]nonacosa-1(29),4,6,8,17,20,22,24,27-nonaene-3,10,26-trione)

Structure for NP0157947 ((2r,11s,13r)-22-chloro-2,5,28-trihydroxy-21-methoxy-7-methyl-14,16,19-trioxa-6-azaheptacyclo[15.11.1.0²,¹¹.0⁴,⁹.0¹³,²⁹.0¹⁸,²⁷.0²⁰,²⁵]nonacosa-1(29),4,6,8,17,20,22,24,27-nonaene-3,10,26-trione)

3D Structure for NP0157947 ((2r,11s,13r)-22-chloro-2,5,28-trihydroxy-21-methoxy-7-methyl-14,16,19-trioxa-6-azaheptacyclo[15.11.1.0²,¹¹.0⁴,⁹.0¹³,²⁹.0¹⁸,²⁷.0²⁰,²⁵]nonacosa-1(29),4,6,8,17,20,22,24,27-nonaene-3,10,26-trione)