3,6-Dioxy-tropan

Details

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Internal ID 35c46a7b-0779-4dfd-aae8-f98ab9db45c7
Taxonomy Alkaloids and derivatives > Tropane alkaloids
IUPAC Name 8-methyl-8-azabicyclo[3.2.1]octane-3,6-diol
SMILES (Canonical) CN1C2CC(CC1C(C2)O)O
SMILES (Isomeric) CN1C2CC(CC1C(C2)O)O
InChI InChI=1S/C8H15NO2/c1-9-5-2-6(10)4-7(9)8(11)3-5/h5-8,10-11H,2-4H2,1H3
InChI Key QWVUOVZJBNQSNS-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C8H15NO2
Molecular Weight 157.21 g/mol
Exact Mass 157.110278721 g/mol
Topological Polar Surface Area (TPSA) 43.70 Ų
XlogP -0.20
Atomic LogP (AlogP) -0.43
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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SCHEMBL1427292

2D Structure

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2D Structure of 3,6-Dioxy-tropan

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9710 97.10%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Lysosomes 0.7107 71.07%
OATP2B1 inhibitior - 0.8509 85.09%
OATP1B1 inhibitior + 0.9660 96.60%
OATP1B3 inhibitior + 0.9465 94.65%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.9639 96.39%
P-glycoprotein inhibitior - 0.9860 98.60%
P-glycoprotein substrate - 0.7949 79.49%
CYP3A4 substrate - 0.6095 60.95%
CYP2C9 substrate + 0.5706 57.06%
CYP2D6 substrate + 0.5446 54.46%
CYP3A4 inhibition - 0.9935 99.35%
CYP2C9 inhibition - 0.9393 93.93%
CYP2C19 inhibition - 0.9279 92.79%
CYP2D6 inhibition - 0.8939 89.39%
CYP1A2 inhibition - 0.8916 89.16%
CYP2C8 inhibition - 0.9964 99.64%
CYP inhibitory promiscuity - 0.9910 99.10%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6465 64.65%
Eye corrosion - 0.9634 96.34%
Eye irritation + 0.7332 73.32%
Skin irritation - 0.7486 74.86%
Skin corrosion - 0.8887 88.87%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6232 62.32%
Micronuclear - 0.5800 58.00%
Hepatotoxicity + 0.5698 56.98%
skin sensitisation - 0.8633 86.33%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity - 0.7074 70.74%
Acute Oral Toxicity (c) III 0.6257 62.57%
Estrogen receptor binding - 0.8317 83.17%
Androgen receptor binding - 0.8361 83.61%
Thyroid receptor binding - 0.8068 80.68%
Glucocorticoid receptor binding - 0.8312 83.12%
Aromatase binding - 0.8766 87.66%
PPAR gamma - 0.9214 92.14%
Honey bee toxicity - 0.8937 89.37%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity - 0.9388 93.88%

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 92.96% 96.09%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 88.78% 97.21%
CHEMBL238 Q01959 Dopamine transporter 86.56% 95.88%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.21% 97.25%
CHEMBL2581 P07339 Cathepsin D 84.28% 98.95%
CHEMBL1907598 P05106 Integrin alpha-V/beta-3 81.03% 95.71%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.48% 97.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.35% 96.95%

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.
Datura innoxia
Schizanthus hookeri

Cross-Links

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PubChem 13855893
LOTUS LTS0057740
wikiData Q105229423