Molecule

ID:132982

General Information
Structure
MolImage
Molecular Formula
C₇₀H₁₁₂N₂₄O₂₃
Molecular Mass
1657.78528
Exact Mass
1656.83321596
Charge
0
InChI
InChI=1S/C70H112N24O23/c1-33(2)53(92-62(110)47(28-52(101)102)85-50(98)30-80-59(107)43(20-21-51(99)100)87-55(103)34(3)82-58(106)41(72)26-38-16-18-40(97)19-17-38)65(113)90-46(27-39-29-77-32-81-39)61(109)83-36(5)57(105)93-54(37(6)96)66(114)91-48(31-95)63(111)88-44(12-7-8-22-71)67(115)94-25-11-15-49(94)64(112)84-35(4)56(104)86-42(13-9-23-78-69(73)74)60(108)89-45(68(116)117)14-10-24-79-70(75)76/h16-19,29,32-37,41-49,53-54,95-97H,7-15,20-28,30-31,71-72H2,1-6H3,(H,77,81)(H,80,107)(H,82,106)(H,83,109)(H,84,112)(H,85,98)(H,86,104)(H,87,103)(H,88,111)(H,89,108)(H,90,113)(H,91,114)(H,92,110)(H,93,105)(H,99,100)(H,101,102)(H,116,117)(H4,73,74,78)(H4,75,76,79)/t34-,35-,36-,37+,41-,42-,43-,44-,45-,46-,47-,48-,49-,53-,54-/m0/s1
InChIKey
JJNXAJMLWIIHBK-QOECIXTQSA-N
Canonic Smiles
NCCCC[C@@H](C(=O)N1CCC[C@H]1C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)O)CCCNC(=N)N)CCCNC(=N)N)C)NC(=O)[C@@H](NC(=O)[C@H]([C@H](O)C)NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](C(C)C)NC(=O)[C@@H](NC(=O)CNC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](Cc1ccc(cc1)O)N)C)CCC(=O)O)CC(=O)O)Cc1nc[nH]c1)C)CO
Isomeric Smiles
C[C@H]([C@@H](C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCCN)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](C(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)CNC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](Cc1ccc(cc1)O)N)O
Calculated Properties
JChem
Acid pKa
3.0924344
H Acceptors
32
H Donor
28
LogD (pH = 5.5)
-19.72173
LogD (pH = 7.4)
-17.303562
Log P
-16.803595
Molar Refractivity
426.9434
Polarizability
158.5555
Polar Surface Area
775.72
Rotatable Bonds
52
Lipinski's Rule of Five
false
Data Source
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Names and Identifiers
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Registration numbers
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Properties
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Related Proteins
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Molecular Spectra
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Molecule Details
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References
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Bioactivity
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