[3-acetyloxy-8a-(acetyloxymethyl)-6-hydroxy-8-(3-hydroxy-3-methylpent-4-enyl)-4,4-dimethyl-7-methylidene-2,3,4a,5,6,8-hexahydro-1H-naphthalen-2-yl] 2-methylbut-2-enoate

Details

• Internal ID: b6f5d2e4-e979-45f0-b14f-fe79479cc4d7
• Taxonomy: Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
• IUPAC Name: [3-acetyloxy-8a-(acetyloxymethyl)-6-hydroxy-8-(3-hydroxy-3-methylpent-4-enyl)-4,4-dimethyl-7-methylidene-2,3,4a,5,6,8-hexahydro-1H-naphthalen-2-yl] 2-methylbut-2-enoate
• SMILES (Canonical): CC=C(C)C(=O)OC1CC2(C(CC(C(=C)C2CCC(C)(C=C)O)O)C(C1OC(=O)C)(C)C)COC(=O)C
• SMILES (Isomeric): CC=C(C)C(=O)OC1CC2(C(CC(C(=C)C2CCC(C)(C=C)O)O)C(C1OC(=O)C)(C)C)COC(=O)C
• InChI: InChI=1S/C29H44O8/c1-10-17(3)26(33)37-23-15-29(16-35-19(5)30)21(12-13-28(9,34)11-2)18(4)22(32)14-24(29)27(7,8)25(23)36-20(6)31/h10-11,21-25,32,34H,2,4,12-16H2,1,3,5-9H3
• InChI Key: XCBRVAGJLFQTMN-UHFFFAOYSA-N
• Popularity: 0 references in papers

Physical and Chemical Properties

• Molecular Formula: C₂₉H₄₄O₈
• Molecular Weight: 520.70 g/mol
• Exact Mass: 520.30361836 g/mol
• Topological Polar Surface Area (TPSA): 119.00 Ų
• XlogP: 3.60
• Atomic LogP (AlogP): 4.05
• H-Bond Acceptor: 8
• H-Bond Donor: 2
• Rotatable Bonds: 9

Synonyms

There are no found synonyms.

2D Structure

ADMET Properties (via admetSAR 2)

Target	Value	Probability (raw)	Probability (%)
Human Intestinal Absorption	+	0.9849	98.49%
Caco-2	-	0.7172	71.72%
Blood Brain Barrier	+	0.6000	60.00%
Human oral bioavailability	-	0.6143	61.43%
Subcellular localzation	Mitochondria	0.9038	90.38%
OATP2B1 inhibitior	-	1.0000	100.00%
OATP1B1 inhibitior	+	0.8436	84.36%
OATP1B3 inhibitior	+	0.8545	85.45%
MATE1 inhibitior	-	0.9000	90.00%
OCT2 inhibitior	-	0.6025	60.25%
BSEP inhibitior	+	0.9739	97.39%
P-glycoprotein inhibitior	+	0.7447	74.47%
P-glycoprotein substrate	+	0.5591	55.91%
CYP3A4 substrate	+	0.7006	70.06%
CYP2C9 substrate	-	0.8046	80.46%
CYP2D6 substrate	-	0.9092	90.92%
CYP3A4 inhibition	-	0.6632	66.32%
CYP2C9 inhibition	-	0.7966	79.66%
CYP2C19 inhibition	-	0.8888	88.88%
CYP2D6 inhibition	-	0.9354	93.54%
CYP1A2 inhibition	-	0.8968	89.68%
CYP2C8 inhibition	+	0.5864	58.64%
CYP inhibitory promiscuity	-	0.8986	89.86%
UGT catelyzed	-	0.5000	50.00%
Carcinogenicity (binary)	-	0.9800	98.00%
Carcinogenicity (trinary)	Non-required	0.7284	72.84%
Eye corrosion	-	0.9925	99.25%
Eye irritation	-	0.9125	91.25%
Skin irritation	+	0.5202	52.02%
Skin corrosion	-	0.9663	96.63%
Ames mutagenesis	-	0.5800	58.00%
Human Ether-a-go-go-Related Gene inhibition	+	0.7685	76.85%
Micronuclear	-	0.8000	80.00%
Hepatotoxicity	-	0.6592	65.92%
skin sensitisation	-	0.7749	77.49%
Respiratory toxicity	+	0.6111	61.11%
Reproductive toxicity	+	0.8889	88.89%
Mitochondrial toxicity	+	0.7375	73.75%
Nephrotoxicity	+	0.5828	58.28%
Acute Oral Toxicity (c)	III	0.6696	66.96%
Estrogen receptor binding	+	0.7953	79.53%
Androgen receptor binding	+	0.6237	62.37%
Thyroid receptor binding	+	0.5554	55.54%
Glucocorticoid receptor binding	+	0.8130	81.30%
Aromatase binding	+	0.7231	72.31%
PPAR gamma	+	0.7054	70.54%
Honey bee toxicity	-	0.5478	54.78%
Biodegradation	-	0.7000	70.00%
Crustacea aquatic toxicity	-	0.5000	50.00%
Fish aquatic toxicity	+	1.0000	100.00%

Targets

Proven Targets:

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	95.34%	91.11%
CHEMBL3251	P19838	Nuclear factor NF-kappa-B p105 subunit	95.10%	96.09%
CHEMBL253	P34972	Cannabinoid CB2 receptor	94.53%	97.25%
CHEMBL2996	Q05655	Protein kinase C delta	94.38%	97.79%
CHEMBL3137262	O60341	LSD1/CoREST complex	90.37%	97.09%
CHEMBL221	P23219	Cyclooxygenase-1	90.22%	90.17%
CHEMBL2007	P16234	Platelet-derived growth factor receptor alpha	90.12%	91.07%
CHEMBL5966	P55899	IgG receptor FcRn large subunit p51	90.11%	90.93%
CHEMBL1841	P06241	Tyrosine-protein kinase FYN	90.01%	81.29%
CHEMBL1293249	Q13887	Kruppel-like factor 5	89.51%	86.33%
CHEMBL4793	Q86TI2	Dipeptidyl peptidase IX	88.53%	96.95%
CHEMBL2581	P07339	Cathepsin D	86.24%	98.95%
CHEMBL335	P18031	Protein-tyrosine phosphatase 1B	86.01%	95.17%
CHEMBL340	P08684	Cytochrome P450 3A4	84.58%	91.19%
CHEMBL1994	P08235	Mineralocorticoid receptor	83.21%	100.00%
CHEMBL3091268	Q92753	Nuclear receptor ROR-beta	83.09%	95.50%
CHEMBL5608	Q16288	NT-3 growth factor receptor	82.61%	95.89%
CHEMBL3807	P17706	T-cell protein-tyrosine phosphatase	82.03%	93.00%
CHEMBL3060	Q9Y345	Glycine transporter 2	81.73%	99.17%
CHEMBL1907602	P06493	Cyclin-dependent kinase 1/cyclin B1	80.65%	91.24%
CHEMBL4657	Q6V1X1	Dipeptidyl peptidase VIII	80.05%	97.21%

Plants that contains it

• Waitzia acuminata

Cross-Links

• PubChem: 162881364
• LOTUS: LTS0228164
• wikiData: Q105324874