(3E,6S,7S,10E,14S,21R,26Z)-4,11,27-trimethyl-17,31,33,35-tetraoxo-14-prop-1-en-2-ylpentacyclo[27.2.2.16,23.115,19.07,21]pentatriaconta-1(32),3,10,15,18,23(34),26,29-octaene-7-carbaldehyde

Details

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Internal ID 473f8a4a-3ee5-4189-9e82-3f3fabe82c62
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name (3E,6S,7S,10E,14S,21R,26Z)-4,11,27-trimethyl-17,31,33,35-tetraoxo-14-prop-1-en-2-ylpentacyclo[27.2.2.16,23.115,19.07,21]pentatriaconta-1(32),3,10,15,18,23(34),26,29-octaene-7-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C42H48O5/c1-26(2)37-14-12-27(3)9-7-15-42(25-43)34-17-29(5)11-13-31-22-40(46)32(23-39(31)45)16-28(4)8-6-10-30(18-34)19-35(42)20-33-21-36(44)24-38(37)41(33)47/h8-9,11,18,21-25,34-35,37H,1,6-7,10,12-17,19-20H2,2-5H3/b27-9+,28-8-,29-11+/t34-,35+,37-,42+/m0/s1
InChI Key IQYUYMLTDIXDMM-CNOSJURISA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C42H48O5
Molecular Weight 632.80 g/mol
Exact Mass 632.35017463 g/mol
Topological Polar Surface Area (TPSA) 85.40 Ų
XlogP 6.20
Atomic LogP (AlogP) 8.70
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3E,6S,7S,10E,14S,21R,26Z)-4,11,27-trimethyl-17,31,33,35-tetraoxo-14-prop-1-en-2-ylpentacyclo[27.2.2.16,23.115,19.07,21]pentatriaconta-1(32),3,10,15,18,23(34),26,29-octaene-7-carbaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9946 99.46%
Caco-2 - 0.7942 79.42%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.6642 66.42%
OATP2B1 inhibitior + 0.7148 71.48%
OATP1B1 inhibitior + 0.8752 87.52%
OATP1B3 inhibitior + 0.9161 91.61%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 0.5000 50.00%
BSEP inhibitior + 1.0000 100.00%
P-glycoprotein inhibitior + 0.9004 90.04%
P-glycoprotein substrate + 0.6293 62.93%
CYP3A4 substrate + 0.7083 70.83%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8698 86.98%
CYP3A4 inhibition - 0.7611 76.11%
CYP2C9 inhibition - 0.6986 69.86%
CYP2C19 inhibition - 0.8398 83.98%
CYP2D6 inhibition - 0.9291 92.91%
CYP1A2 inhibition - 0.8117 81.17%
CYP2C8 inhibition + 0.6999 69.99%
CYP inhibitory promiscuity - 0.8844 88.44%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5898 58.98%
Eye corrosion - 0.9812 98.12%
Eye irritation - 0.9270 92.70%
Skin irritation - 0.5372 53.72%
Skin corrosion - 0.9637 96.37%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8008 80.08%
Micronuclear - 0.8100 81.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation + 0.5054 50.54%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity + 0.8511 85.11%
Acute Oral Toxicity (c) III 0.7812 78.12%
Estrogen receptor binding + 0.7970 79.70%
Androgen receptor binding + 0.7054 70.54%
Thyroid receptor binding + 0.5559 55.59%
Glucocorticoid receptor binding + 0.8614 86.14%
Aromatase binding + 0.6219 62.19%
PPAR gamma + 0.7256 72.56%
Honey bee toxicity - 0.7545 75.45%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5051 50.51%
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
CHEMBL1951 P21397 Monoamine oxidase A 97.68% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.15% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.38% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.86% 97.25%
CHEMBL218 P21554 Cannabinoid CB1 receptor 91.29% 96.61%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.00% 89.00%
CHEMBL2581 P07339 Cathepsin D 90.36% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.88% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.98% 99.23%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.26% 95.89%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.11% 96.09%
CHEMBL1902 P62942 FK506-binding protein 1A 83.07% 97.05%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 81.72% 86.00%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 81.53% 93.00%
CHEMBL5028 O14672 ADAM10 81.14% 97.50%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.07% 95.89%
CHEMBL1859 O95180 Voltage-gated T-type calcium channel alpha-1H subunit 81.02% 98.57%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 80.62% 97.33%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.08% 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.
There are no matching plants.

Cross-Links

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PubChem 163104457
LOTUS LTS0259190
wikiData Q105118708