1,2,5,5-Tetramethyl-1,3-cyclopentadiene

Details

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Internal ID 45b5878f-f626-44b7-b6b5-ee665f9eb7b2
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name 1,2,5,5-tetramethylcyclopenta-1,3-diene
SMILES (Canonical) CC1=C(C(C=C1)(C)C)C
SMILES (Isomeric) CC1=C(C(C=C1)(C)C)C
InChI InChI=1S/C9H14/c1-7-5-6-9(3,4)8(7)2/h5-6H,1-4H3
InChI Key FZQSOBIGZJECPN-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C9H14
Molecular Weight 122.21 g/mol
Exact Mass 122.109550447 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.92
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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FZQSOBIGZJECPN-UHFFFAOYSA-N
1,2,5,5-Tetramethyl-1,3-cyclopentadiene #
1,3-Cyclopentadiene, 1,2,5,5-tetramethyl-

2D Structure

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2D Structure of 1,2,5,5-Tetramethyl-1,3-cyclopentadiene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9891 98.91%
Caco-2 + 0.8727 87.27%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.8429 84.29%
Subcellular localzation Lysosomes 0.6186 61.86%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9457 94.57%
OATP1B3 inhibitior + 0.9263 92.63%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8321 83.21%
P-glycoprotein inhibitior - 0.9748 97.48%
P-glycoprotein substrate - 0.9738 97.38%
CYP3A4 substrate - 0.6829 68.29%
CYP2C9 substrate - 0.6202 62.02%
CYP2D6 substrate - 0.8230 82.30%
CYP3A4 inhibition - 0.8269 82.69%
CYP2C9 inhibition - 0.8275 82.75%
CYP2C19 inhibition - 0.8194 81.94%
CYP2D6 inhibition - 0.9400 94.00%
CYP1A2 inhibition - 0.8487 84.87%
CYP2C8 inhibition - 0.9927 99.27%
CYP inhibitory promiscuity + 0.5235 52.35%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5417 54.17%
Carcinogenicity (trinary) Warning 0.5368 53.68%
Eye corrosion + 0.6981 69.81%
Eye irritation + 0.9778 97.78%
Skin irritation + 0.7073 70.73%
Skin corrosion - 0.8301 83.01%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7377 73.77%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.7750 77.50%
skin sensitisation + 0.8989 89.89%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.7111 71.11%
Mitochondrial toxicity - 0.6305 63.05%
Nephrotoxicity + 0.5430 54.30%
Acute Oral Toxicity (c) III 0.8354 83.54%
Estrogen receptor binding - 0.9049 90.49%
Androgen receptor binding - 0.9123 91.23%
Thyroid receptor binding - 0.8179 81.79%
Glucocorticoid receptor binding - 0.8941 89.41%
Aromatase binding - 0.8591 85.91%
PPAR gamma - 0.8920 89.20%
Honey bee toxicity - 0.9670 96.70%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.7800 78.00%
Fish aquatic toxicity + 0.9492 94.92%

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
CHEMBL5697 Q9GZT9 Egl nine homolog 1 93.52% 93.40%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 90.05% 85.30%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.14% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 82.95% 94.75%

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.
Cnidium monnieri
Scleromitrion diffusum
Scutellaria barbata

Cross-Links

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PubChem 572142
NPASS NPC86941