1,2,3,4,5-Pentamethylcyclopentadiene

Details

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Internal ID 42dc8925-957a-4e31-af54-4a076d520e00
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name 1,2,3,4,5-pentamethylcyclopenta-1,3-diene
SMILES (Canonical) CC1C(=C(C(=C1C)C)C)C
SMILES (Isomeric) CC1C(=C(C(=C1C)C)C)C
InChI InChI=1S/C10H16/c1-6-7(2)9(4)10(5)8(6)3/h6H,1-5H3
InChI Key WQIQNKQYEUMPBM-UHFFFAOYSA-N
Popularity 130 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16
Molecular Weight 136.23 g/mol
Exact Mass 136.125200510 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 1.90
Atomic LogP (AlogP) 3.31
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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1,2,3,4,5-Pentamethylcyclopentadiene
1,2,3,4,5-pentamethylcyclopenta-1,3-diene
Pentamethylcyclopentadiene
Cyclopentadiene, 1,2,3,4,5-pentamethyl-
1,3-Cyclopentadiene, 1,2,3,4,5-pentamethyl-
1,3-Cyclopentadiene, pentamethyl-
1,2,3,4,5-Pentamethyl-1,3-cyclopentadiene
DSE3MRZ77C
EINECS 223-743-4
NSC-222823
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1,2,3,4,5-Pentamethylcyclopentadiene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9927 99.27%
Caco-2 - 0.5210 52.10%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.9143 91.43%
Subcellular localzation Lysosomes 0.5983 59.83%
OATP2B1 inhibitior - 0.8660 86.60%
OATP1B1 inhibitior + 0.9664 96.64%
OATP1B3 inhibitior + 0.9503 95.03%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9190 91.90%
P-glycoprotein inhibitior - 0.9620 96.20%
P-glycoprotein substrate - 0.9728 97.28%
CYP3A4 substrate - 0.7560 75.60%
CYP2C9 substrate - 0.8074 80.74%
CYP2D6 substrate - 0.8164 81.64%
CYP3A4 inhibition - 0.8923 89.23%
CYP2C9 inhibition - 0.8858 88.58%
CYP2C19 inhibition - 0.8290 82.90%
CYP2D6 inhibition - 0.9187 91.87%
CYP1A2 inhibition - 0.7954 79.54%
CYP2C8 inhibition - 0.9879 98.79%
CYP inhibitory promiscuity + 0.5061 50.61%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5417 54.17%
Carcinogenicity (trinary) Warning 0.5118 51.18%
Eye corrosion + 0.8208 82.08%
Eye irritation + 0.9709 97.09%
Skin irritation + 0.7994 79.94%
Skin corrosion - 0.7764 77.64%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7499 74.99%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.7500 75.00%
skin sensitisation + 0.8925 89.25%
Respiratory toxicity - 0.8444 84.44%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity + 0.4611 46.11%
Acute Oral Toxicity (c) III 0.6284 62.84%
Estrogen receptor binding - 0.8499 84.99%
Androgen receptor binding - 0.7992 79.92%
Thyroid receptor binding - 0.7148 71.48%
Glucocorticoid receptor binding - 0.8611 86.11%
Aromatase binding - 0.7691 76.91%
PPAR gamma - 0.8402 84.02%
Honey bee toxicity - 0.9164 91.64%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.7000 70.00%
Fish aquatic toxicity + 0.9293 92.93%

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
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 84.44% 86.00%

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.
Chrysanthemum indicum
Schisandra chinensis

Cross-Links

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PubChem 77667
NPASS NPC82399