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162105731 molecular structure
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ChemBase ID: 106676
Molecular Formular: C73H118N16O27
Molecular Mass: 1651.80902
Monoisotopic Mass: 1650.8352326
SMILES and InChIs

SMILES:
CC[C@H](C)[C@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@@H](N)CCCCN)[C@@H](C)O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](CC(C)C)[C@@H](O)CC(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](Cc1ccccc1)C(=O)O
Canonical SMILES:
NCCCC[C@@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H]([C@H](CC(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)O)Cc1ccccc1)CCC(=O)O)C)C(C)C)O)CC(C)C)CC(=O)N)C(C)C)CCC(=O)O)CO)[C@H](CC)C)CCC(=O)O)CCC(=O)O)[C@H](O)C)N
InChI:
InChI=1S/C73H118N16O27/c1-11-37(8)59(88-66(108)45(23-27-56(101)102)79-63(105)43(21-25-54(97)98)81-72(114)60(39(10)91)89-62(104)41(75)19-15-16-28-74)71(113)85-49(33-90)68(110)80-44(22-26-55(99)100)65(107)87-58(36(6)7)70(112)83-47(31-51(76)93)67(109)82-46(29-34(2)3)50(92)32-52(94)86-57(35(4)5)69(111)77-38(9)61(103)78-42(20-24-53(95)96)64(106)84-48(73(115)116)30-40-17-13-12-14-18-40/h12-14,17-18,34-39,41-50,57-60,90-92H,11,15-16,19-33,74-75H2,1-10H3,(H2,76,93)(H,77,111)(H,78,103)(H,79,105)(H,80,110)(H,81,114)(H,82,109)(H,83,112)(H,84,106)(H,85,113)(H,86,94)(H,87,107)(H,88,108)(H,89,104)(H,95,96)(H,97,98)(H,99,100)(H,101,102)(H,115,116)/t37-,38-,39+,41-,42-,43-,44-,45-,46-,47-,48-,49-,50-,57-,58-,59-,60-/m0/s1
InChIKey:
CQTBDEGWLSDJEP-JMAXQNTPSA-N

Cite this record

CBID:106676 http://www.chembase.cn/molecule-106676.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
Synonyms
Lys-Thr-Glu-Glu-Ile-Ser-Glu-Val-Asn(STATINE)-Val-Ala-Glu-Phe-OH
LTEEISEVD(STATINE)VAEF-OH
Lys-Thr-Glu-Glu-Ile-Ser-Glu-Val-Asn(STATINE)-Val-Ala-Glu-Phe-OH
PubChem SID
162105731
PubChem CID
16149643

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID Price
MP Biomedicals
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Data Source Data ID
PubChem 16149643 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 2.874119  H Acceptors 29 
H Donor 24  LogD (pH = 5.5) -15.956926 
LogD (pH = 7.4) -20.999943  Log P -11.809896 
Molar Refractivity 401.6683 cm3 Polarizability 158.93611 Å3
Polar Surface Area 720.62 Å2 Rotatable Bonds 57 
Lipinski's Rule of Five false 

PROPERTIES

PROPERTIES

Safety Information Product Information Bioassay(PubChem)
MSDS Link
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Certificate of Analysis
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DETAILS

DETAILS

MP Biomedicals MP Biomedicals
MP Biomedicals - 03STA200 external link
An inhibitor for secretase

REFERENCES

REFERENCES

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  • • Sinha, S. et al., Nature, 402:537 (1999).
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PATENTS

PATENTS

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INTERNET

INTERNET

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