4-[[(2S,3R,4R,4aR,8aR)-3-(hydroxymethyl)-4-[(E)-5-hydroxy-3-methylpent-3-enyl]-4,8,8a-trimethyl-1,2,3,4a,5,6-hexahydronaphthalen-2-yl]oxy]-4-oxobutanoic acid

Details

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Internal ID 347ee858-654e-4ef5-bf70-6239013b6338
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Colensane and clerodane diterpenoids
IUPAC Name 4-[[(2S,3R,4R,4aR,8aR)-3-(hydroxymethyl)-4-[(E)-5-hydroxy-3-methylpent-3-enyl]-4,8,8a-trimethyl-1,2,3,4a,5,6-hexahydronaphthalen-2-yl]oxy]-4-oxobutanoic acid
SMILES (Canonical) CC1=CCCC2C1(CC(C(C2(C)CCC(=CCO)C)CO)OC(=O)CCC(=O)O)C
SMILES (Isomeric) CC1=CCC[C@H]2[C@]1(C[C@@H]([C@H]([C@]2(C)CC/C(=C/CO)/C)CO)OC(=O)CCC(=O)O)C
InChI InChI=1S/C24H38O6/c1-16(11-13-25)10-12-23(3)18(15-26)19(30-22(29)9-8-21(27)28)14-24(4)17(2)6-5-7-20(23)24/h6,11,18-20,25-26H,5,7-10,12-15H2,1-4H3,(H,27,28)/b16-11+/t18-,19+,20-,23+,24+/m1/s1
InChI Key KFWNRUNSSBZDEP-MUFKJQONSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C24H38O6
Molecular Weight 422.60 g/mol
Exact Mass 422.26683893 g/mol
Topological Polar Surface Area (TPSA) 104.00 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.86
H-Bond Acceptor 5
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 4-[[(2S,3R,4R,4aR,8aR)-3-(hydroxymethyl)-4-[(E)-5-hydroxy-3-methylpent-3-enyl]-4,8,8a-trimethyl-1,2,3,4a,5,6-hexahydronaphthalen-2-yl]oxy]-4-oxobutanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9778 97.78%
Caco-2 - 0.5302 53.02%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.8652 86.52%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8788 87.88%
OATP1B3 inhibitior + 0.8453 84.53%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6140 61.40%
BSEP inhibitior + 0.7224 72.24%
P-glycoprotein inhibitior - 0.4921 49.21%
P-glycoprotein substrate - 0.6794 67.94%
CYP3A4 substrate + 0.6467 64.67%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.8819 88.19%
CYP3A4 inhibition - 0.6695 66.95%
CYP2C9 inhibition - 0.8930 89.30%
CYP2C19 inhibition - 0.8982 89.82%
CYP2D6 inhibition - 0.9434 94.34%
CYP1A2 inhibition - 0.8399 83.99%
CYP2C8 inhibition + 0.4669 46.69%
CYP inhibitory promiscuity - 0.9291 92.91%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6616 66.16%
Eye corrosion - 0.9932 99.32%
Eye irritation - 0.9427 94.27%
Skin irritation - 0.5470 54.70%
Skin corrosion - 0.9717 97.17%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6834 68.34%
Micronuclear - 0.8100 81.00%
Hepatotoxicity - 0.6449 64.49%
skin sensitisation - 0.8982 89.82%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.5976 59.76%
Acute Oral Toxicity (c) III 0.6292 62.92%
Estrogen receptor binding + 0.7702 77.02%
Androgen receptor binding + 0.6014 60.14%
Thyroid receptor binding + 0.6604 66.04%
Glucocorticoid receptor binding + 0.8137 81.37%
Aromatase binding + 0.7316 73.16%
PPAR gamma + 0.5433 54.33%
Honey bee toxicity - 0.8476 84.76%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6755 67.55%
Fish aquatic toxicity + 0.9893 98.93%

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
CHEMBL4040 P28482 MAP kinase ERK2 98.90% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.09% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.83% 91.11%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 94.05% 94.23%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 93.41% 94.62%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 93.01% 94.08%
CHEMBL221 P23219 Cyclooxygenase-1 89.79% 90.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.99% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.84% 97.09%
CHEMBL2581 P07339 Cathepsin D 88.40% 98.95%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 88.40% 93.00%
CHEMBL340 P08684 Cytochrome P450 3A4 88.28% 91.19%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.64% 86.33%
CHEMBL211 P08172 Muscarinic acetylcholine receptor M2 85.44% 94.97%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.65% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.08% 95.56%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 82.25% 95.50%
CHEMBL5255 O00206 Toll-like receptor 4 80.93% 92.50%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.15% 96.00%

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.
Baccharis pteronioides

Cross-Links

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PubChem 14633062
LOTUS LTS0120089
wikiData Q105140585