Stachene

Details

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Internal ID a6e44a6c-2f6e-4917-847f-7bc21d8a1fb1
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name (1R,4R,9R,10S,13R)-5,5,9,13-tetramethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-ene
SMILES (Canonical) CC1(CCCC2(C1CCC34C2CCC(C3)(C=C4)C)C)C
SMILES (Isomeric) C[C@@]12CC[C@H]3[C@@]4(CCCC([C@H]4CC[C@@]3(C1)C=C2)(C)C)C
InChI InChI=1S/C20H32/c1-17(2)8-5-9-19(4)15(17)7-11-20-13-12-18(3,14-20)10-6-16(19)20/h12-13,15-16H,5-11,14H2,1-4H3/t15-,16+,18+,19-,20+/m1/s1
InChI Key GXMKKDDGINQVBE-QVHQYWGISA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C20H32
Molecular Weight 272.50 g/mol
Exact Mass 272.250401021 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 7.50
Atomic LogP (AlogP) 5.98
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Stachene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9945 99.45%
Caco-2 + 0.8840 88.40%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Lysosomes 0.7038 70.38%
OATP2B1 inhibitior - 0.8549 85.49%
OATP1B1 inhibitior + 0.8985 89.85%
OATP1B3 inhibitior + 0.9483 94.83%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.5218 52.18%
P-glycoprotein inhibitior - 0.8265 82.65%
P-glycoprotein substrate - 0.9232 92.32%
CYP3A4 substrate + 0.5359 53.59%
CYP2C9 substrate - 0.7979 79.79%
CYP2D6 substrate - 0.7660 76.60%
CYP3A4 inhibition - 0.9267 92.67%
CYP2C9 inhibition - 0.8009 80.09%
CYP2C19 inhibition - 0.7368 73.68%
CYP2D6 inhibition - 0.9436 94.36%
CYP1A2 inhibition - 0.8433 84.33%
CYP2C8 inhibition - 0.7418 74.18%
CYP inhibitory promiscuity - 0.7367 73.67%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7500 75.00%
Carcinogenicity (trinary) Non-required 0.5074 50.74%
Eye corrosion - 0.8973 89.73%
Eye irritation - 0.8085 80.85%
Skin irritation - 0.5925 59.25%
Skin corrosion - 0.9470 94.70%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4207 42.07%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5959 59.59%
skin sensitisation + 0.7888 78.88%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity - 0.5778 57.78%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.5525 55.25%
Acute Oral Toxicity (c) III 0.7455 74.55%
Estrogen receptor binding + 0.6559 65.59%
Androgen receptor binding + 0.5907 59.07%
Thyroid receptor binding + 0.6205 62.05%
Glucocorticoid receptor binding - 0.4949 49.49%
Aromatase binding - 0.5000 50.00%
PPAR gamma - 0.6082 60.82%
Honey bee toxicity - 0.8364 83.64%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5100 51.00%
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
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.11% 97.25%
CHEMBL4040 P28482 MAP kinase ERK2 94.06% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.29% 96.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 88.33% 82.69%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 86.71% 96.38%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.38% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.86% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.13% 91.11%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.52% 95.89%
CHEMBL1937 Q92769 Histone deacetylase 2 83.11% 94.75%
CHEMBL4370 P16662 UDP-glucuronosyltransferase 2B7 83.09% 100.00%
CHEMBL5203 P33316 dUTP pyrophosphatase 81.96% 99.18%
CHEMBL4072 P07858 Cathepsin B 81.51% 93.67%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.48% 92.94%

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.
Manihot esculenta

Cross-Links

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PubChem 12304253
LOTUS LTS0040517
wikiData Q105023193