N-[2-[[(1S,2S)-1-[[(1S,2S)-1-[[(1S)-5-amino-1-[[(1S)-5-amino-1-[[(1S,2S)-1-[[(1S,2S)-1-[[(1S)-5-amino-1-[[(1S)-5-amino-1-[[(1S,2S)-1-[[(1S,2S)-1-[[(1S)-5-amino-1-[[(1S)-5-amino-1-[[(1S,2S)-1-[[(1S)-2-amino-2-oxo-1-[[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxymethyl]ethyl]carbamoyl]-2-methyl-butyl]carbamoyl]pentyl]carbamoyl]pentyl]carbamoyl]-2-methyl-butyl]carbamoyl]-2-methyl-butyl]carbamoyl]pentyl]carbamoyl]pentyl]carbamoyl]-2-methyl-butyl]carbamoyl]-2-methyl-butyl]carbamoyl]pentyl]carbamoyl]pentyl]carbamoyl]-2-methyl-butyl]carbamoyl]-2-methyl-butyl]amino]-2-oxo-ethyl]octanamide

ID: ALA5277970

Chembl Id: CHEMBL5277970

Max Phase: Preclinical

Molecular Formula: C97H184N22O22

Molecular Weight: 2010.67

Names and Identifiers

Canonical SMILES:  CCCCCCCC(=O)NCC(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@H](C(=O)N[C@@H](CO[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O)C(N)=O)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC

Standard InChI:  InChI=1S/C97H184N22O22/c1-16-24-25-26-27-46-71(121)105-53-72(122)113-73(56(9)17-2)94(137)117-75(58(11)19-4)90(133)109-63(40-28-34-47-98)85(128)107-67(44-32-38-51-102)88(131)115-78(61(14)22-7)96(139)119-77(60(13)21-6)92(135)111-65(42-30-36-49-100)86(129)108-68(45-33-39-52-103)89(132)116-79(62(15)23-8)95(138)118-76(59(12)20-5)91(134)110-64(41-29-35-48-99)84(127)106-66(43-31-37-50-101)87(130)114-74(57(10)18-3)93(136)112-69(83(104)126)55-140-97-82(125)81(124)80(123)70(54-120)141-97/h56-70,73-82,97,120,123-125H,16-55,98-103H2,1-15H3,(H2,104,126)(H,105,121)(H,106,127)(H,107,128)(H,108,129)(H,109,133)(H,110,134)(H,111,135)(H,112,136)(H,113,122)(H,114,130)(H,115,131)(H,116,132)(H,117,137)(H,118,138)(H,119,139)/t56-,57-,58-,59-,60-,61-,62-,63-,64-,65-,66-,67-,68-,69-,70+,73-,74-,75-,76-,77-,78-,79-,80-,81-,82+,97+/m0/s1

Standard InChI Key:  YFZGRZMMFAWIOK-ZQYLTBJOSA-N

Alternative Forms

1. Parent:

   

   ALA5277970

   ---

Molecule Features

Natural Product: No

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type:

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Calculated Properties

Molecular Weight: 2010.67

Molecular Weight (Monoisotopic): 2009.3956

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References

1. Cao R, Li L, Xu Z, Li J, Wu D, Wang Y, Zhu H..  (2023)  The lipidation and glycosylation enabling bioactivity enhancement and structural change of antibacterial peptide G3.,  90  [PMID:37182609] [10.1016/j.bmcl.2023.129322]

Source

Source(1):

• Scientific Literature