EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Free-form
UNII	2BR5PL6H39
EPA CompTox	DTXSID701016176

Keyword(s):

Human Metabolites

Molecule Category

Free-form

UNII

2BR5PL6H39

EPA CompTox

DTXSID701016176


InChI Key	YKAVHPRGGAUFDN-JTQLBUQXSA-N
Smiles	CC[C@H]1OC(=O)[C@H](C)[C@@H](O[C@H]2C[C@@](C)(OC)[C@@H](O)[C@H](C)O2)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)C[C@@H]([C@H]2O)N(C)C)[C@@]2(C)C[C@@H](C)[C@]3(O2)O[C@@]1(C)[C@H](O)[C@H]3C
InChI	InChI=1S/C37H65NO12/c1-14-25-36(10)29(40)22(6)37(50-36)18(2)16-35(9,49-37)31(48-33-27(39)24(38(11)12)15-19(3)44-33)20(4)28(21(5)32(42)46-25)47-26-17-34(8,43-13)30(41)23(7)45-26/h18-31,33,39-41H,14-17H2,1-13H3/t18-,19-,20+,21-,22-,23+,24+,25-,26+,27-,28+,29-,30+,31-,33+,34-,35-,36-,37+/m1/s1

InChI Key

YKAVHPRGGAUFDN-JTQLBUQXSA-N

Smiles

CC[C@H]1OC(=O)[C@H](C)[C@@H](O[C@H]2C[C@@](C)(OC)[C@@H](O)[C@H](C)O2)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)C[C@@H]([C@H]2O)N(C)C)[C@@]2(C)C[C@@H](C)[C@]3(O2)O[C@@]1(C)[C@H](O)[C@H]3C

InChI

InChI=1S/C37H65NO12/c1-14-25-36(10)29(40)22(6)37(50-36)18(2)16-35(9,49-37)31(48-33-27(39)24(38(11)12)15-19(3)44-33)20(4)28(21(5)32(42)46-25)47-26-17-34(8,43-13)30(41)23(7)45-26/h18-31,33,39-41H,14-17H2,1-13H3/t18-,19-,20+,21-,22-,23+,24+,25-,26+,27-,28+,29-,30+,31-,33+,34-,35-,36-,37+/m1/s1

Property Name	Value
Molecular Formula	C37H65N1O12
Molecular Weight	715.45
AlogP	2.99
Hydrogen Bond Acceptor	13.0
Hydrogen Bond Donor	3.0
Number of Rotational Bond	7.0
Polar Surface Area	154.84
Heavy Atoms	50.0

Property Name

Value

Molecular Formula

C37H65N1O12

Molecular Weight

715.45

AlogP

2.99

Hydrogen Bond Acceptor

13.0

Hydrogen Bond Donor

3.0

Number of Rotational Bond

7.0

Polar Surface Area

154.84

Heavy Atoms

50.0

Resources	Reference
CAS NUMBER	23893-13-2
NORMAN SUSDAT
FDA SRS	2BR5PL6H39
PubChem	83949
ChemSpider	30988539.0

Resources

Reference

CAS NUMBER

23893-13-2

NORMAN SUSDAT

FDA SRS

2BR5PL6H39

PubChem

83949

ChemSpider

30988539.0

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

ANHYDROERYTHROMYCIN A

Structure

Physicochemical Descriptors

Cross References