Amorpha-4,7(11)-diene

Details

Top
Internal ID e41e0450-8c27-4e0f-9db0-4b5a8dbbad37
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1R,4aR,8aS)-1,6-dimethyl-4-propan-2-ylidene-2,3,4a,7,8,8a-hexahydro-1H-naphthalene
SMILES (Canonical) CC1CCC(=C(C)C)C2C1CCC(=C2)C
SMILES (Isomeric) C[C@@H]1CCC(=C(C)C)[C@@H]2[C@H]1CCC(=C2)C
InChI InChI=1S/C15H24/c1-10(2)13-8-6-12(4)14-7-5-11(3)9-15(13)14/h9,12,14-15H,5-8H2,1-4H3/t12-,14+,15-/m1/s1
InChI Key YBEONGKDMARZSS-VHDGCEQUSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H24
Molecular Weight 204.35 g/mol
Exact Mass 204.187800766 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.50
Atomic LogP (AlogP) 4.73
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

Top
YBEONGKDMARZSS-VHDGCEQUSA-N

2D Structure

Top
2D Structure of Amorpha-4,7(11)-diene

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9957 99.57%
Caco-2 + 0.9687 96.87%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Lysosomes 0.5552 55.52%
OATP2B1 inhibitior - 0.8431 84.31%
OATP1B1 inhibitior + 0.9478 94.78%
OATP1B3 inhibitior + 0.9274 92.74%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.8843 88.43%
P-glycoprotein inhibitior - 0.9317 93.17%
P-glycoprotein substrate - 0.8794 87.94%
CYP3A4 substrate - 0.5483 54.83%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7217 72.17%
CYP3A4 inhibition - 0.9141 91.41%
CYP2C9 inhibition - 0.7740 77.40%
CYP2C19 inhibition - 0.6805 68.05%
CYP2D6 inhibition - 0.9235 92.35%
CYP1A2 inhibition - 0.7008 70.08%
CYP2C8 inhibition - 0.8234 82.34%
CYP inhibitory promiscuity - 0.5618 56.18%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7800 78.00%
Carcinogenicity (trinary) Non-required 0.4519 45.19%
Eye corrosion - 0.8556 85.56%
Eye irritation + 0.6693 66.93%
Skin irritation - 0.5381 53.81%
Skin corrosion - 0.9045 90.45%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7374 73.74%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.7054 70.54%
skin sensitisation + 0.8967 89.67%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity - 0.8116 81.16%
Acute Oral Toxicity (c) III 0.6941 69.41%
Estrogen receptor binding - 0.9567 95.67%
Androgen receptor binding + 0.5646 56.46%
Thyroid receptor binding - 0.6713 67.13%
Glucocorticoid receptor binding - 0.8604 86.04%
Aromatase binding - 0.8792 87.92%
PPAR gamma - 0.8381 83.81%
Honey bee toxicity - 0.9148 91.48%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.78% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.23% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.84% 100.00%
CHEMBL2581 P07339 Cathepsin D 82.81% 98.95%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.55% 92.94%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.51% 95.56%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 80.14% 97.33%

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.
Hypericum perforatum
Zingiber officinale

Cross-Links

Top
PubChem 91753509
NPASS NPC297528