D-Mannuronicacidlactone

Details

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Internal ID 334b8ab9-8fce-4b63-8593-276a8580647c
Taxonomy Organoheterocyclic compounds > Dioxepanes > 1,4-dioxepanes
IUPAC Name 3,4,8-trihydroxy-2,6-dioxabicyclo[3.2.1]octan-7-one
SMILES (Canonical) C1(C2C(C(OC1C(=O)O2)O)O)O
SMILES (Isomeric) C1(C2C(C(OC1C(=O)O2)O)O)O
InChI InChI=1S/C6H8O6/c7-1-3-2(8)5(9)12-4(1)6(10)11-3/h1-5,7-9H
InChI Key NNKCVJYUFBVOMM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C6H8O6
Molecular Weight 176.12 g/mol
Exact Mass 176.03208797 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP -2.10
Atomic LogP (AlogP) -2.65
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 0

Synonyms

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7424-09-1
SCHEMBL20156770

2D Structure

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2D Structure of D-Mannuronicacidlactone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.4688 46.88%
Caco-2 - 0.9259 92.59%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.5789 57.89%
OATP2B1 inhibitior - 0.8629 86.29%
OATP1B1 inhibitior + 0.9310 93.10%
OATP1B3 inhibitior + 0.9541 95.41%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9820 98.20%
P-glycoprotein inhibitior - 0.9679 96.79%
P-glycoprotein substrate - 0.9864 98.64%
CYP3A4 substrate - 0.6455 64.55%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8684 86.84%
CYP3A4 inhibition - 0.6758 67.58%
CYP2C9 inhibition - 0.9633 96.33%
CYP2C19 inhibition - 0.8812 88.12%
CYP2D6 inhibition - 0.9349 93.49%
CYP1A2 inhibition - 0.8696 86.96%
CYP2C8 inhibition - 0.9916 99.16%
CYP inhibitory promiscuity - 0.9578 95.78%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6801 68.01%
Eye corrosion - 0.9560 95.60%
Eye irritation - 0.8259 82.59%
Skin irritation - 0.5395 53.95%
Skin corrosion - 0.9100 91.00%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8366 83.66%
Micronuclear + 0.6100 61.00%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation - 0.8711 87.11%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity - 0.5889 58.89%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity + 0.7647 76.47%
Acute Oral Toxicity (c) IV 0.5630 56.30%
Estrogen receptor binding - 0.7810 78.10%
Androgen receptor binding - 0.8377 83.77%
Thyroid receptor binding - 0.6490 64.90%
Glucocorticoid receptor binding - 0.8639 86.39%
Aromatase binding - 0.8185 81.85%
PPAR gamma - 0.7996 79.96%
Honey bee toxicity - 0.7810 78.10%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity - 0.6471 64.71%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.91% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.21% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.20% 99.23%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Prunus avium

Cross-Links

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PubChem 14178454
LOTUS LTS0001714
wikiData Q105182186