ID: ALA4282474

Max Phase: Preclinical

Molecular Formula: C52H74N4O17

Molecular Weight: 1027.17

Molecule Type: Small molecule

Representations

Canonical SMILES:  COC[C@@H](OC)C(=O)O[C@H](CC[C@H](C)[C@H](C[C@@H]1OC(=O)C[C@@H](O)C/C=C/C(=O)[C@H](C)[C@H](OC)c2coc(n2)-c2coc(n2)-c2coc(n2)/C=C/C[C@H](OC)[C@H]1C)OC)[C@H](C)[C@H](OC(C)=O)[C@H](C)/C=C/N(C)C=O

Standard InChI:  InChI=1S/C52H74N4O17/c1-30(19-20-42(73-52(62)45(66-11)28-63-8)34(5)48(71-35(6)58)31(2)21-22-56(7)29-57)43(65-10)24-44-33(4)41(64-9)17-14-18-46-53-38(26-68-46)50-55-39(27-70-50)51-54-37(25-69-51)49(67-12)32(3)40(60)16-13-15-36(59)23-47(61)72-44/h13-14,16,18,21-22,25-27,29-34,36,41-45,48-49,59H,15,17,19-20,23-24,28H2,1-12H3/b16-13+,18-14+,22-21+/t30-,31+,32-,33+,34-,36-,41-,42+,43-,44-,45+,48+,49-/m0/s1

Standard InChI Key:  ZYDMLFOHENLMIN-GTNGWFEESA-N

Molecule Features

Natural Product: No

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type: Small molecule

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Properties

Molecular Weight: 1027.17

Molecular Weight (Monoisotopic): 1026.5049

AlogP:

#Rotatable Bonds:

Polar Surface Area:

Molecular Species:

HBA:

HBD:

#RO5 Violations:

HBA (Lipinski):

HBD (Lipinski):

#RO5 Violations (Lipinski):

CX Acidic pKa:

CX Basic pKa:

CX LogP:

CX LogD:

Aromatic Rings:

Heavy Atoms:

QED Weighted:

Np Likeness Score:

References

1. Suo R, Takada K, Kohtsuka H, Ise Y, Okada S, Matsunaga S..  (2018)  Miuramides A and B, Trisoxazole Macrolides from a Mycale sp. Marine Sponge That Induce a Protrusion Phenotype in Cultured Mammalian Cells.,  81  (4): [PMID:29613787] [10.1021/acs.jnatprod.8b00101]

2. Hirayama Y,Yamagishi K,Suzuki T,Kawagishi H,Kita M,Kigoshi H.  (2016)  Analysis of the aplyronine A-induced protein-protein interaction between actin and tubulin by surface plasmon resonance.,  24  (12.0): [PMID:27161875] [10.1016/j.bmc.2016.04.049]

Source

Source(1):

• Scientific Literature