SCS-C004325

chartarlactam B

Pathway: Terpenoids Superclass: Meroterpenoids Class: Spriromeroterpenoids | Tetraketide meroterpenoids

Chemical Structure

Structure of chartarlactam B
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3D conformers are computationally generated from SMILES by RDKit for visualization and download; they are not experimental crystal or NMR structures.
Download: SDF SMILES

Source Information

Stachybotrys chartarum (soft coral-derived fungus)
Weizhou Island
DOI: 10.1021/np400824u  · Journal of Natural Products

Drug-likeness (Lipinski Ro5)

Molecular Weight
485.6 Da
Threshold ≤ 500
ALogP
4.51
Threshold ≤ 5
H-Bond Donors
3
Threshold ≤ 5
H-Bond Acceptors
5
Threshold ≤ 10
Passes Lipinski Rule of Five — drug-like candidate

Chemical Properties

Molecular Formula:
C28H39NO6
Molecular Weight:
485.6210 Da
SMILES:
C[C@@H]1CC[C@H]2C(C)(C)[C@H](O)CC[C@]2(C)[C@@]12Cc1c(O)cc3c(c1O2)CN(CCCCC(=O)O)C3=O
InChIKey:
OPCQWQMQPFYESC-SELUXCBJSA-N
InChI:
InChI=1S/C28H39NO6/c1-16-8-9-21-26(2,3)22(31)10-11-27(21,4)28(16)14-18-20(30)13-17-19(24(18)35-28)15-29(25(17)34)12-6-5-7-23(32)33/h13,16,21-22,30-31H,5-12,14-15H2,1-4H3,(H,32,33)/t16-,21+,22-,27+,28-/m1/s1
Calculated Properties
ALogP:
4.510 lipophilicity
TPSA:
107.30 Ų polar surface area
H-Bond Donors:
3
H-Bond Acceptors:
5
Rotatable Bonds:
5
Ring Count:
5 (1 aromatic)
Chiral Centers:
5
Fsp³:
0.7143 fraction sp³ carbon

Database Information

Compound ID:
SCS-C004325
NPClassifier Pathway:
Terpenoids
NPClassifier Superclass:
Meroterpenoids
NPClassifier Class:
Spriromeroterpenoids Tetraketide meroterpenoids
Glycoside:
No
NPClassifier Status:
Classified
External Links:

Biological Activity Data

No bioactivity data available for this compound.

Structure enlarged