EcoDrugPlus


Synonyms	Juvidex Mannose 6-phosphate Mannose-6-phosphate
Status
Molecule Category	UNKNOWN
UNII	C77UQ006XD

Synonyms

Juvidex

Mannose 6-phosphate

Mannose-6-phosphate

Status

Molecule Category

UNKNOWN

UNII

C77UQ006XD


Active Pharmaceutical Ingredients Bioactive chemicals	Exact Similarity SubStructure	Threshold (%) >= 70


InChI Key	NBSCHQHZLSJFNQ-PQMKYFCFSA-N
Smiles	O=P(O)(O)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O)[C@@H]1O
InChI	InChI=1S/C6H13O9P/c7-3-2(1-14-16(11,12)13)15-6(10)5(9)4(3)8/h2-10H,1H2,(H2,11,12,13)/t2-,3-,4+,5+,6+/m1/s1

InChI Key

NBSCHQHZLSJFNQ-PQMKYFCFSA-N

Smiles

O=P(O)(O)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O)[C@@H]1O

InChI

InChI=1S/C6H13O9P/c7-3-2(1-14-16(11,12)13)15-6(10)5(9)4(3)8/h2-10H,1H2,(H2,11,12,13)/t2-,3-,4+,5+,6+/m1/s1

Property Name	Value
Molecular Formula	C6H13O9P
Molecular Weight	260.13
AlogP	-3.1
Hydrogen Bond Acceptor	7.0
Hydrogen Bond Donor	6.0
Number of Rotational Bond	3.0
Polar Surface Area	156.91
Molecular species	ACID
Aromatic Rings	0.0
Heavy Atoms	16.0

Property Name

Value

Molecular Formula

C6H13O9P

Molecular Weight

260.13

AlogP

-3.1

Hydrogen Bond Acceptor

7.0

Hydrogen Bond Donor

6.0

Number of Rotational Bond

3.0

Polar Surface Area

156.91

Molecular species

ACID

Aromatic Rings

0.0

Heavy Atoms

16.0

Resources	Reference
ChEBI	43896
ChEMBL	CHEMBL402001
DrugBank	DB02900
FDA SRS	C77UQ006XD
PDB	M6P
SureChEMBL	SCHEMBL742653
ZINC	ZINC000004096188

Resources

Reference

ChEBI

ChEMBL

DrugBank

FDA SRS

PDB

SureChEMBL

ZINC


PREMIER has received funding from the 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 this manuscript contains. Elements of the website have been developed under projects PREMIER and the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT is thanked for providing computational resources. Content of the website is provided without guarantee for correctness. Data has been collected and integrated from multiple public sources, for the largest: FDA, HUGO Gene Nomenclature Committee, ChEMBL, IUPHAR/BPS guide to pharmacology, Reactome, UniProt, and Ensembl. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).

PREMIER has received funding from the 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 this manuscript contains.

Elements of the website have been developed under projects PREMIER and the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT is thanked for providing computational resources. Content of the website is provided without guarantee for correctness. Data has been collected and integrated from multiple public sources, for the largest: FDA, HUGO Gene Nomenclature Committee, ChEMBL, IUPHAR/BPS guide to pharmacology, Reactome, UniProt, and Ensembl. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).

MANNOSE-6-PHOSPHATE

Structure

Physicochemical Descriptors

Cross References