2,2-Dimethylchroman

Details

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Internal ID 908cbe2d-3e2b-4f2a-9713-d1e12d9799d7
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > 2,2-dimethyl-1-benzopyrans
IUPAC Name 2,2-dimethyl-3,4-dihydrochromene
SMILES (Canonical) CC1(CCC2=CC=CC=C2O1)C
SMILES (Isomeric) CC1(CCC2=CC=CC=C2O1)C
InChI InChI=1S/C11H14O/c1-11(2)8-7-9-5-3-4-6-10(9)12-11/h3-6H,7-8H2,1-2H3
InChI Key MITIYLBEZOKYLX-UHFFFAOYSA-N
Popularity 50 references in papers

Physical and Chemical Properties

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Molecular Formula C11H14O
Molecular Weight 162.23 g/mol
Exact Mass 162.104465066 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.79
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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2H-1-Benzopyran, 3,4-dihydro-2,2-dimethyl-
Chroman, 2,2-dimethyl-
DTXSID00152598
NSC 63863
RefChem:243559
DTXCID4075089
MITIYLBEZOKYLX-UHFFFAOYSA-N
1198-96-5
2,2-Dimethylchromane
2,2-dimethyl-3,4-dihydro-2H-1-benzopyran
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2,2-Dimethylchroman

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9960 99.60%
Caco-2 + 0.9467 94.67%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.5213 52.13%
OATP2B1 inhibitior - 0.8661 86.61%
OATP1B1 inhibitior + 0.9434 94.34%
OATP1B3 inhibitior + 0.9742 97.42%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.9469 94.69%
P-glycoprotein inhibitior - 0.9888 98.88%
P-glycoprotein substrate - 0.9725 97.25%
CYP3A4 substrate - 0.5732 57.32%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate + 0.5000 50.00%
CYP3A4 inhibition - 0.8064 80.64%
CYP2C9 inhibition - 0.8233 82.33%
CYP2C19 inhibition + 0.5188 51.88%
CYP2D6 inhibition - 0.8206 82.06%
CYP1A2 inhibition + 0.7276 72.76%
CYP2C8 inhibition - 0.9347 93.47%
CYP inhibitory promiscuity - 0.6911 69.11%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Non-required 0.5947 59.47%
Eye corrosion - 0.9150 91.50%
Eye irritation + 0.8426 84.26%
Skin irritation - 0.5278 52.78%
Skin corrosion - 0.9127 91.27%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5332 53.32%
Micronuclear - 0.9241 92.41%
Hepatotoxicity + 0.5322 53.22%
skin sensitisation + 0.5972 59.72%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.5529 55.29%
Acute Oral Toxicity (c) III 0.8165 81.65%
Estrogen receptor binding - 0.8704 87.04%
Androgen receptor binding - 0.7709 77.09%
Thyroid receptor binding - 0.8941 89.41%
Glucocorticoid receptor binding - 0.9182 91.82%
Aromatase binding - 0.8910 89.10%
PPAR gamma - 0.9116 91.16%
Honey bee toxicity - 0.9112 91.12%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.7500 75.00%
Fish aquatic toxicity + 0.7957 79.57%

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 96.22% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.95% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.29% 95.56%
CHEMBL2581 P07339 Cathepsin D 88.28% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.92% 93.99%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.36% 86.33%
CHEMBL3902 P09211 Glutathione S-transferase Pi 80.90% 93.81%

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 persica

Cross-Links

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PubChem 136936
NPASS NPC29272