1,3-Dimethyladamantane

Details

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Internal ID 9a9226ed-e747-40b8-b3c4-a287df2a8b5b
Taxonomy Hydrocarbons > Polycyclic hydrocarbons
IUPAC Name 1,3-dimethyladamantane
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H20/c1-11-4-9-3-10(5-11)7-12(2,6-9)8-11/h9-10H,3-8H2,1-2H3
InChI Key CWNOIUTVJRWADX-UHFFFAOYSA-N
Popularity 92 references in papers

Physical and Chemical Properties

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Molecular Formula C12H20
Molecular Weight 164.29 g/mol
Exact Mass 164.156500638 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.60
Atomic LogP (AlogP) 3.61
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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702-79-4
Adamantane, 1,3-dimethyl-
1,3-dimethyltricyclo[3.3.1.13,7]decane
96G4OD5Z59
1,3-Dimethyltricyclo(3.3.1.13,7)decane
DTXSID1049439
CHEBI:47900
1,3-dimethyltricyclo[3.3.1.1(3,7)]decane
1,3-dimethyltricyclo(3.3.1.1(3,7))decane
RefChem:414687
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1,3-Dimethyladamantane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9944 99.44%
Caco-2 + 0.7443 74.43%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.8571 85.71%
Subcellular localzation Lysosomes 0.8520 85.20%
OATP2B1 inhibitior - 0.8640 86.40%
OATP1B1 inhibitior + 0.9659 96.59%
OATP1B3 inhibitior + 0.9536 95.36%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8203 82.03%
P-glycoprotein inhibitior - 0.9737 97.37%
P-glycoprotein substrate - 0.9414 94.14%
CYP3A4 substrate - 0.6089 60.89%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.7731 77.31%
CYP3A4 inhibition - 0.8420 84.20%
CYP2C9 inhibition - 0.9063 90.63%
CYP2C19 inhibition - 0.9056 90.56%
CYP2D6 inhibition - 0.9402 94.02%
CYP1A2 inhibition - 0.8928 89.28%
CYP2C8 inhibition - 0.9852 98.52%
CYP inhibitory promiscuity - 0.7947 79.47%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5900 59.00%
Carcinogenicity (trinary) Non-required 0.4803 48.03%
Eye corrosion - 0.7208 72.08%
Eye irritation + 0.9368 93.68%
Skin irritation - 0.5325 53.25%
Skin corrosion - 0.8927 89.27%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7563 75.63%
Micronuclear - 0.8326 83.26%
Hepatotoxicity - 0.5324 53.24%
skin sensitisation + 0.8110 81.10%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity - 0.6889 68.89%
Mitochondrial toxicity - 0.6576 65.76%
Nephrotoxicity + 0.6893 68.93%
Acute Oral Toxicity (c) IV 0.5190 51.90%
Estrogen receptor binding - 0.8925 89.25%
Androgen receptor binding - 0.5213 52.13%
Thyroid receptor binding - 0.7891 78.91%
Glucocorticoid receptor binding - 0.8929 89.29%
Aromatase binding - 0.7623 76.23%
PPAR gamma - 0.8592 85.92%
Honey bee toxicity - 0.8010 80.10%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9702 97.02%

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 92.28% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.14% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.93% 97.09%
CHEMBL240 Q12809 HERG 85.39% 89.76%
CHEMBL2996 Q05655 Protein kinase C delta 80.80% 97.79%
CHEMBL238 Q01959 Dopamine transporter 80.22% 95.88%

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.
Artemisia annua
Artemisia carvifolia

Cross-Links

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PubChem 12800
NPASS NPC278878