Hexamethylcyclotrisiloxane

Details

Top
Internal ID ef19bb92-f680-4ad4-aee9-2e89460507d2
Taxonomy Organometallic compounds > Organometalloid compounds > Organosilicon compounds > Organoheterosilanes
IUPAC Name 2,2,4,4,6,6-hexamethyl-1,3,5,2,4,6-trioxatrisilinane
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H18O3Si3/c1-10(2)7-11(3,4)9-12(5,6)8-10/h1-6H3
InChI Key HTDJPCNNEPUOOQ-UHFFFAOYSA-N
Popularity 426 references in papers

Physical and Chemical Properties

Top
Molecular Formula C6H18O3Si3
Molecular Weight 222.46 g/mol
Exact Mass 222.05637404 g/mol
Topological Polar Surface Area (TPSA) 27.70 Ų
XlogP 0.00
Atomic LogP (AlogP) 2.16
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

Top
541-05-9
Cyclotrisiloxane, hexamethyl-
Dimethylsiloxane cyclic trimer
SDK 10
DTXSID6027185
EPV75L8O0R
DC 246
LS 8120
DTXCID307185
RefChem:786203
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of Hexamethylcyclotrisiloxane

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8720 87.20%
Caco-2 + 0.5554 55.54%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Mitochondria 0.6285 62.85%
OATP2B1 inhibitior - 0.8650 86.50%
OATP1B1 inhibitior + 0.9701 97.01%
OATP1B3 inhibitior + 0.9571 95.71%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9382 93.82%
P-glycoprotein inhibitior - 0.9721 97.21%
P-glycoprotein substrate - 0.9900 99.00%
CYP3A4 substrate - 0.7774 77.74%
CYP2C9 substrate - 0.7829 78.29%
CYP2D6 substrate - 0.7930 79.30%
CYP3A4 inhibition - 0.9320 93.20%
CYP2C9 inhibition - 0.8840 88.40%
CYP2C19 inhibition - 0.8216 82.16%
CYP2D6 inhibition - 0.9324 93.24%
CYP1A2 inhibition - 0.7397 73.97%
CYP2C8 inhibition - 0.9901 99.01%
CYP inhibitory promiscuity - 0.9518 95.18%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7219 72.19%
Carcinogenicity (trinary) Non-required 0.5769 57.69%
Eye corrosion + 0.7709 77.09%
Eye irritation + 1.0000 100.00%
Skin irritation - 0.8720 87.20%
Skin corrosion - 0.9640 96.40%
Ames mutagenesis - 0.9900 99.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7926 79.26%
Micronuclear - 0.5100 51.00%
Hepatotoxicity + 0.9052 90.52%
skin sensitisation - 0.7420 74.20%
Respiratory toxicity - 0.8667 86.67%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity - 0.6872 68.72%
Nephrotoxicity + 0.7915 79.15%
Acute Oral Toxicity (c) III 0.5054 50.54%
Estrogen receptor binding - 0.8811 88.11%
Androgen receptor binding - 0.9080 90.80%
Thyroid receptor binding - 0.8249 82.49%
Glucocorticoid receptor binding - 0.9107 91.07%
Aromatase binding - 0.7569 75.69%
PPAR gamma - 0.7078 70.78%
Honey bee toxicity - 0.8896 88.96%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity - 0.8558 85.58%

Targets

Top

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
No predicted targets yet!

Plants that contains it

Top
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.
Hedychium yunnanense

Cross-Links

Top
PubChem 10914
NPASS NPC188413