3-[(3S,3aR,5aS,6S,7S,9aR,9bR)-3-[(2S,5S)-2,5-dihydroxy-6-methylhept-6-en-2-yl]-6,9a,9b-trimethyl-7-prop-1-en-2-yl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoic acid

Details

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Internal ID 185b0594-10f9-4eb9-9251-d7249ea78128
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesterterpenoids
IUPAC Name 3-[(3S,3aR,5aS,6S,7S,9aR,9bR)-3-[(2S,5S)-2,5-dihydroxy-6-methylhept-6-en-2-yl]-6,9a,9b-trimethyl-7-prop-1-en-2-yl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoic acid
SMILES (Canonical) CC(=C)C1CCC2(C(C1(C)CCC(=O)O)CCC3C2(CCC3C(C)(CCC(C(=C)C)O)O)C)C
SMILES (Isomeric) CC(=C)[C@@H]1CC[C@@]2([C@H]([C@@]1(C)CCC(=O)O)CC[C@H]3[C@]2(CC[C@@H]3[C@](C)(CC[C@@H](C(=C)C)O)O)C)C
InChI InChI=1S/C30H50O4/c1-19(2)21-11-17-29(7)25(27(21,5)15-14-26(32)33)10-9-22-23(12-16-28(22,29)6)30(8,34)18-13-24(31)20(3)4/h21-25,31,34H,1,3,9-18H2,2,4-8H3,(H,32,33)/t21-,22+,23-,24-,25-,27-,28+,29+,30-/m0/s1
InChI Key HHLNMULUIBCHEA-BEQPVHHASA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H50O4
Molecular Weight 474.70 g/mol
Exact Mass 474.37091007 g/mol
Topological Polar Surface Area (TPSA) 77.80 Ų
XlogP 7.60
Atomic LogP (AlogP) 6.76
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-[(3S,3aR,5aS,6S,7S,9aR,9bR)-3-[(2S,5S)-2,5-dihydroxy-6-methylhept-6-en-2-yl]-6,9a,9b-trimethyl-7-prop-1-en-2-yl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9899 98.99%
Caco-2 - 0.6511 65.11%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.6670 66.70%
OATP2B1 inhibitior - 0.5680 56.80%
OATP1B1 inhibitior + 0.8606 86.06%
OATP1B3 inhibitior - 0.2455 24.55%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior + 0.8080 80.80%
P-glycoprotein inhibitior - 0.5636 56.36%
P-glycoprotein substrate + 0.5121 51.21%
CYP3A4 substrate + 0.6840 68.40%
CYP2C9 substrate - 0.8151 81.51%
CYP2D6 substrate - 0.8662 86.62%
CYP3A4 inhibition - 0.7145 71.45%
CYP2C9 inhibition - 0.9055 90.55%
CYP2C19 inhibition - 0.9268 92.68%
CYP2D6 inhibition - 0.9550 95.50%
CYP1A2 inhibition - 0.8929 89.29%
CYP2C8 inhibition + 0.4543 45.43%
CYP inhibitory promiscuity - 0.8160 81.60%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.6864 68.64%
Eye corrosion - 0.9935 99.35%
Eye irritation - 0.9109 91.09%
Skin irritation + 0.6050 60.50%
Skin corrosion - 0.9655 96.55%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3999 39.99%
Micronuclear - 0.8500 85.00%
Hepatotoxicity - 0.6698 66.98%
skin sensitisation - 0.5393 53.93%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.8750 87.50%
Nephrotoxicity - 0.7864 78.64%
Acute Oral Toxicity (c) III 0.6201 62.01%
Estrogen receptor binding + 0.6471 64.71%
Androgen receptor binding + 0.7494 74.94%
Thyroid receptor binding + 0.5527 55.27%
Glucocorticoid receptor binding + 0.7417 74.17%
Aromatase binding + 0.6844 68.44%
PPAR gamma + 0.6885 68.85%
Honey bee toxicity - 0.7702 77.02%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6800 68.00%
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 99.15% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.65% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.65% 91.11%
CHEMBL218 P21554 Cannabinoid CB1 receptor 95.98% 96.61%
CHEMBL2581 P07339 Cathepsin D 95.66% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.06% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.70% 97.09%
CHEMBL4227 P25090 Lipoxin A4 receptor 89.10% 100.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.81% 85.14%
CHEMBL4040 P28482 MAP kinase ERK2 86.66% 83.82%
CHEMBL340 P08684 Cytochrome P450 3A4 83.58% 91.19%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 83.31% 89.05%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.21% 96.95%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.54% 95.89%
CHEMBL5285 Q99683 Mitogen-activated protein kinase kinase kinase 5 82.33% 92.26%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.20% 100.00%
CHEMBL5028 O14672 ADAM10 80.74% 97.50%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.52% 100.00%

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.
Alnus japonica

Cross-Links

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PubChem 162929479
LOTUS LTS0162869
wikiData Q105028357