Viscumitol

Details

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Internal ID 552eb9f3-d861-4b0b-9e56-04c10fab9fe8
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Secondary alcohols > Cyclohexanols
IUPAC Name (1R,2S,3R,4S,5R,6S)-5,6-dimethoxycyclohexane-1,2,3,4-tetrol
SMILES (Canonical) COC1C(C(C(C(C1OC)O)O)O)O
SMILES (Isomeric) CO[C@@H]1[C@H]([C@@H]([C@@H]([C@H]([C@@H]1OC)O)O)O)O
InChI InChI=1S/C8H16O6/c1-13-7-5(11)3(9)4(10)6(12)8(7)14-2/h3-12H,1-2H3/t3-,4+,5+,6-,7-,8+
InChI Key HREVPIABJKTEDU-CNVXYERZSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C8H16O6
Molecular Weight 208.21 g/mol
Exact Mass 208.09468823 g/mol
Topological Polar Surface Area (TPSA) 99.40 Ų
XlogP -2.60
Atomic LogP (AlogP) -2.53
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 2

Synonyms

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DTXSID70726664
145680-48-4
Q7935898

2D Structure

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2D Structure of Viscumitol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7258 72.58%
Caco-2 - 0.8412 84.12%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.7133 71.33%
OATP2B1 inhibitior - 0.8622 86.22%
OATP1B1 inhibitior + 0.9663 96.63%
OATP1B3 inhibitior + 0.9777 97.77%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9640 96.40%
P-glycoprotein inhibitior - 0.9426 94.26%
P-glycoprotein substrate - 0.9858 98.58%
CYP3A4 substrate - 0.6861 68.61%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7322 73.22%
CYP3A4 inhibition - 0.8970 89.70%
CYP2C9 inhibition - 0.9237 92.37%
CYP2C19 inhibition - 0.9093 90.93%
CYP2D6 inhibition - 0.9230 92.30%
CYP1A2 inhibition - 0.8864 88.64%
CYP2C8 inhibition - 0.9853 98.53%
CYP inhibitory promiscuity - 0.8981 89.81%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8123 81.23%
Carcinogenicity (trinary) Non-required 0.6809 68.09%
Eye corrosion - 0.8298 82.98%
Eye irritation - 0.7077 70.77%
Skin irritation - 0.5735 57.35%
Skin corrosion - 0.8265 82.65%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6077 60.77%
Micronuclear - 0.5900 59.00%
Hepatotoxicity - 0.8125 81.25%
skin sensitisation - 0.6792 67.92%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity - 0.5613 56.13%
Acute Oral Toxicity (c) III 0.7017 70.17%
Estrogen receptor binding - 0.7846 78.46%
Androgen receptor binding - 0.8667 86.67%
Thyroid receptor binding + 0.5221 52.21%
Glucocorticoid receptor binding - 0.8021 80.21%
Aromatase binding - 0.7029 70.29%
PPAR gamma - 0.7146 71.46%
Honey bee toxicity - 0.7282 72.82%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity - 0.6720 67.20%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.32% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 80.36% 90.17%

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.
Viscum album

Cross-Links

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PubChem 57459394
LOTUS LTS0013476
wikiData Q7935898