[(3R,5S,7R,8R,9S,10S,12S,13R,14S,17R)-7,12-bis[[2-[(2-amino-3-methyl-butanoyl)amino]acetyl]oxy]-10,13-dimethyl-17-[(1R)-1-methyl-4-oxo-4-[[1-[3-[4-[[[(4R)-4-[(3R,5S,7R,8R,9S,10S,12S,13R,14S,17R)-3,7,12-tris[[2-[(2-amino-3-methyl-butanoyl)amino]acetyl]oxy]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]pentanoyl]amino]methyl]triazol-1-yl]propyl]triazol-4-yl]methylamino]butyl]-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl]2-[(2-amino-3-methyl-butanoyl)amino]acetate hexahydrochloride

ID: ALA5180522

Chembl Id: CHEMBL5180522

PubChem CID: 168272807

Max Phase: Preclinical

Molecular Formula: C99H170Cl6N20O20

Molecular Weight: 1954.52

Associated Items:

Names and Identifiers

Canonical SMILES:  CC(C)C(N)C(=O)NCC(=O)O[C@@H]1CC[C@@]2(C)[C@@H](C1)C[C@@H](OC(=O)CNC(=O)C(N)C(C)C)[C@@H]1[C@@H]2C[C@H](OC(=O)CNC(=O)C(N)C(C)C)[C@]2(C)[C@@H]([C@H](C)CCC(=O)NCc3cn(CCCn4cc(CNC(=O)CC[C@@H](C)[C@H]5CC[C@H]6[C@@H]7[C@H](OC(=O)CNC(=O)C(N)C(C)C)C[C@@H]8C[C@H](OC(=O)CNC(=O)C(N)C(C)C)CC[C@]8(C)[C@H]7C[C@H](OC(=O)CNC(=O)C(N)C(C)C)[C@]56C)nn4)nn3)CC[C@@H]12.Cl.Cl.Cl.Cl.Cl.Cl

Standard InChI:  InChI=1S/C99H164N20O20.6ClH/c1-50(2)84(100)90(128)108-42-76(122)134-62-28-30-96(15)58(34-62)36-70(136-78(124)44-110-92(130)86(102)52(5)6)82-66-24-22-64(98(66,17)72(38-68(82)96)138-80(126)46-112-94(132)88(104)54(9)10)56(13)20-26-74(120)106-40-60-48-118(116-114-60)32-19-33-119-49-61(115-117-119)41-107-75(121)27-21-57(14)65-23-25-67-83-69(39-73(99(65,67)18)139-81(127)47-113-95(133)89(105)55(11)12)97(16)31-29-63(135-77(123)43-109-91(129)85(101)51(3)4)35-59(97)37-71(83)137-79(125)45-111-93(131)87(103)53(7)8;;;;;;/h48-59,62-73,82-89H,19-47,100-105H2,1-18H3,(H,106,120)(H,107,121)(H,108,128)(H,109,129)(H,110,130)(H,111,131)(H,112,132)(H,113,133);6*1H/t56-,57-,58+,59+,62-,63-,64-,65-,66+,67+,68+,69+,70-,71-,72+,73+,82+,83+,84?,85?,86?,87?,88?,89?,96+,97+,98-,99-;;;;;;/m1....../s1

Standard InChI Key:  OJVWNCFSWNOHOL-UQPPUXSHSA-N

Associated Targets(non-human)

Enterococcus faecium (13803 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
3LL cell line (138 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cell membrane (1233 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mus musculus (284745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Calculated Properties

Molecular Weight: 1954.52Molecular Weight (Monoisotopic): 1953.2431AlogP: #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. Saini V, Mehta D, Gupta S, Kumar S, Rani P, Rana K, Rajput K, Jain D, Pal G, Aggarwal B, Pal S, Gupta SK, Kumar Y, Ramu VS, Bajaj A..  (2022)  Targeting Vancomycin-Resistant Enterococci (VRE) Infections and Van Operon-Mediated Drug Resistance Using Dimeric Cholic Acid-Peptide Conjugates.,  65  (22.0): [PMID:36331380] [10.1021/acs.jmedchem.2c01293]

Source