EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Free-form
UNII	YN28Z5YZ73
EPA CompTox	DTXSID20978151

Keyword(s):

Human Metabolites

Molecule Category

Free-form

UNII

YN28Z5YZ73

EPA CompTox

DTXSID20978151


InChI Key	ZRZROXNBKJAOKB-GFVHOAGBSA-N
Smiles	C[C@H](NC(=O)[C@@H](N)Cc1c[nH]c2ccccc12)C(=O)NCC(=O)NCC(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](CO)C(=O)NCC(=O)N[C@@H](CCC(O)=O)C(O)=O
InChI	InChI=1S/C35H48N10O15/c1-16(41-32(56)20(36)9-18-11-37-21-6-4-3-5-19(18)21)30(54)39-12-25(47)38-13-26(48)44-23(10-29(52)53)34(58)42-17(2)31(55)45-24(15-46)33(57)40-14-27(49)43-22(35(59)60)7-8-28(50)51/h3-6,11,16-17,20,22-24,37,46H,7-10,12-15,36H2,1-2H3,(H,38,47)(H,39,54)(H,40,57)(H,41,56)(H,42,58)(H,43,49)(H,44,48)(H,45,55)(H,50,51)(H,52,53)(H,59,60)/t16-,17-,20-,22-,23-,24-/m0/s1

InChI Key

ZRZROXNBKJAOKB-GFVHOAGBSA-N

Smiles

C[C@H](NC(=O)[C@@H](N)Cc1c[nH]c2ccccc12)C(=O)NCC(=O)NCC(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](CO)C(=O)NCC(=O)N[C@@H](CCC(O)=O)C(O)=O

InChI

InChI=1S/C35H48N10O15/c1-16(41-32(56)20(36)9-18-11-37-21-6-4-3-5-19(18)21)30(54)39-12-25(47)38-13-26(48)44-23(10-29(52)53)34(58)42-17(2)31(55)45-24(15-46)33(57)40-14-27(49)43-22(35(59)60)7-8-28(50)51/h3-6,11,16-17,20,22-24,37,46H,7-10,12-15,36H2,1-2H3,(H,38,47)(H,39,54)(H,40,57)(H,41,56)(H,42,58)(H,43,49)(H,44,48)(H,45,55)(H,50,51)(H,52,53)(H,59,60)/t16-,17-,20-,22-,23-,24-/m0/s1

Property Name	Value
Molecular Formula	C35H48N10O15
Molecular Weight	848.33
AlogP	0.99
Hydrogen Bond Acceptor	13.0
Hydrogen Bond Donor	14.0
Number of Rotational Bond	25.0
Polar Surface Area	434.66
Heavy Atoms	60.0

Property Name

Value

Molecular Formula

C35H48N10O15

Molecular Weight

848.33

AlogP

0.99

Hydrogen Bond Acceptor

13.0

Hydrogen Bond Donor

14.0

Number of Rotational Bond

25.0

Polar Surface Area

434.66

Heavy Atoms

60.0

Resources	Reference
CAS NUMBER	62568-57-4
NORMAN SUSDAT
FDA SRS	YN28Z5YZ73

Resources

Reference

CAS NUMBER

62568-57-4

NORMAN SUSDAT

FDA SRS

YN28Z5YZ73

EcoDrug+ was developed under the PREMIER Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement No 875508. The JU receives support from the EU’s Horizon 2020 research and innovation programme and the European Federation of Pharmaceutical Industries and Associations (EFPIA). The views reflect only the authors’ perspective and the JU is not responsible for any use that may be made of the information EcoDrug+ contains.

Elements of EcoDrug+ were developed under the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT Center for Science Ltd is thanked for providing computational resources. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).

Content of EcoDrug+ is provided without guarantee for correctness.

Cite Us:

Ashenafi Legehar, Siobhán Monaghan, Mael Briand, Akseli Niemelä, Leo Ghemtio, Ziaurrehman Tanoli, A Ross Brown, Charles R Tyler, Henri Xhaard, EcoDrug PLUS: an advanced database for drug target conservation analysis and environmental risk assessment, Nucleic Acids Research, Volume 54, Issue D1, 6 January 2026, Pages D1397–D1404, https://doi.org/10.1093/nar/gkaf1251

This work is licensed under Creative Commons Attribution-ShareAlike 4.0 International License

Last update: Monday, 3 November 2025

EMIDELTIDE

Structure

Physicochemical Descriptors

Cross References