4,5-Dimethyl-1,2,3,6,7,8,8a,8b-octahydrobiphenylene

Details

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Internal ID 247aa4cd-0ddb-47ec-bc75-322582f532d9
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name 4,5-dimethyl-1,2,3,6,7,8,8a,8b-octahydrobiphenylene
SMILES (Canonical) CC1=C2C(CCC1)C3C2=C(CCC3)C
SMILES (Isomeric) CC1=C2C(CCC1)C3C2=C(CCC3)C
InChI InChI=1S/C14H20/c1-9-5-3-7-11-12-8-4-6-10(2)14(12)13(9)11/h11-12H,3-8H2,1-2H3
InChI Key LPONMLCILIVSGA-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H20
Molecular Weight 188.31 g/mol
Exact Mass 188.156500638 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 2.90
Atomic LogP (AlogP) 4.23
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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106988-87-8
DTXSID60342579
LPONMLCILIVSGA-UHFFFAOYSA-N
4,5-Dimethyl-1,2,3,6,7,8,8a,8b-octahydrobiphenylene #
Biphenylene, 1,2,3,6,7,8,8a,8b-octahydro-4,5-dimethyl-

2D Structure

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2D Structure of 4,5-Dimethyl-1,2,3,6,7,8,8a,8b-octahydrobiphenylene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9954 99.54%
Caco-2 + 0.9420 94.20%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Lysosomes 0.6780 67.80%
OATP2B1 inhibitior - 0.8405 84.05%
OATP1B1 inhibitior + 0.9352 93.52%
OATP1B3 inhibitior + 0.9536 95.36%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.8111 81.11%
P-glycoprotein inhibitior - 0.8534 85.34%
P-glycoprotein substrate - 0.9790 97.90%
CYP3A4 substrate - 0.6969 69.69%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7546 75.46%
CYP3A4 inhibition - 0.8633 86.33%
CYP2C9 inhibition - 0.7810 78.10%
CYP2C19 inhibition - 0.7292 72.92%
CYP2D6 inhibition - 0.8970 89.70%
CYP1A2 inhibition - 0.6316 63.16%
CYP2C8 inhibition - 0.9455 94.55%
CYP inhibitory promiscuity - 0.5749 57.49%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Non-required 0.4064 40.64%
Eye corrosion - 0.8344 83.44%
Eye irritation + 0.8636 86.36%
Skin irritation - 0.5869 58.69%
Skin corrosion - 0.9060 90.60%
Ames mutagenesis - 0.9400 94.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4348 43.48%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.7835 78.35%
skin sensitisation + 0.8530 85.30%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity - 0.5778 57.78%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity + 0.5442 54.42%
Acute Oral Toxicity (c) III 0.7497 74.97%
Estrogen receptor binding - 0.8496 84.96%
Androgen receptor binding + 0.6856 68.56%
Thyroid receptor binding - 0.6411 64.11%
Glucocorticoid receptor binding - 0.7861 78.61%
Aromatase binding - 0.8785 87.85%
PPAR gamma - 0.7958 79.58%
Honey bee toxicity - 0.9700 97.00%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL3137262 O60341 LSD1/CoREST complex 87.94% 97.09%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 83.44% 95.58%
CHEMBL3155 P34969 Serotonin 7 (5-HT7) receptor 81.72% 90.71%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.32% 96.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.23% 95.89%

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.
Bupleurum chinense
Bupleurum falcatum
Bupleurum scorzonerifolium

Cross-Links

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PubChem 583087
NPASS NPC226692