4-[(E)-2-[(1R,4aS,5R,8aR)-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-6-oxo-1,3,4,4a,7,8-hexahydronaphthalen-1-yl]ethenyl]-2H-furan-5-one

Details

• Internal ID: c7df6f87-8870-4efd-a0c1-7c9c08a66dbf
• Taxonomy: Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Diterpene lactones
• IUPAC Name: 4-[(E)-2-[(1R,4aS,5R,8aR)-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-6-oxo-1,3,4,4a,7,8-hexahydronaphthalen-1-yl]ethenyl]-2H-furan-5-one
• SMILES (Canonical): CC12CCC(=O)C(C1CCC(=C)C2C=CC3=CCOC3=O)(C)CO
• SMILES (Isomeric): C[C@@]12CCC(=O)[C@@]([C@H]1CCC(=C)[C@H]2/C=C/C3=CCOC3=O)(C)CO
• InChI: InChI=1S/C20H26O4/c1-13-4-7-16-19(2,10-8-17(22)20(16,3)12-21)15(13)6-5-14-9-11-24-18(14)23/h5-6,9,15-16,21H,1,4,7-8,10-12H2,2-3H3/b6-5+/t15-,16+,19+,20+/m1/s1
• InChI Key: VZUQDSZLBXYRHS-WHCBKWPTSA-N
• Popularity: 2 references in papers

Physical and Chemical Properties

• Molecular Formula: C₂₀H₂₆O₄
• Molecular Weight: 330.40 g/mol
• Exact Mass: 330.18310931 g/mol
• Topological Polar Surface Area (TPSA): 63.60 Ų
• XlogP: 2.90
• Atomic LogP (AlogP): 2.98
• H-Bond Acceptor: 4
• H-Bond Donor: 1
• Rotatable Bonds: 3

Synonyms

There are no found synonyms.

2D Structure

ADMET Properties (via admetSAR 2)

Target	Value	Probability (raw)	Probability (%)
Human Intestinal Absorption	+	0.9632	96.32%
Caco-2	+	0.5312	53.12%
Blood Brain Barrier	+	0.6750	67.50%
Human oral bioavailability	-	0.5286	52.86%
Subcellular localzation	Mitochondria	0.7441	74.41%
OATP2B1 inhibitior	-	1.0000	100.00%
OATP1B1 inhibitior	+	0.8895	88.95%
OATP1B3 inhibitior	+	0.9383	93.83%
MATE1 inhibitior	-	0.9212	92.12%
OCT2 inhibitior	+	0.6412	64.12%
BSEP inhibitior	+	0.6269	62.69%
P-glycoprotein inhibitior	-	0.7283	72.83%
P-glycoprotein substrate	-	0.7586	75.86%
CYP3A4 substrate	+	0.6205	62.05%
CYP2C9 substrate	-	1.0000	100.00%
CYP2D6 substrate	-	0.9120	91.20%
CYP3A4 inhibition	-	0.6477	64.77%
CYP2C9 inhibition	-	0.9135	91.35%
CYP2C19 inhibition	-	0.8917	89.17%
CYP2D6 inhibition	-	0.9434	94.34%
CYP1A2 inhibition	-	0.7769	77.69%
CYP2C8 inhibition	-	0.6115	61.15%
CYP inhibitory promiscuity	-	0.8903	89.03%
UGT catelyzed	+	1.0000	100.00%
Carcinogenicity (binary)	-	1.0000	100.00%
Carcinogenicity (trinary)	Non-required	0.5423	54.23%
Eye corrosion	-	0.9878	98.78%
Eye irritation	-	0.9490	94.90%
Skin irritation	+	0.5403	54.03%
Skin corrosion	-	0.9187	91.87%
Ames mutagenesis	-	0.6424	64.24%
Human Ether-a-go-go-Related Gene inhibition	+	0.6607	66.07%
Micronuclear	-	0.8200	82.00%
Hepatotoxicity	-	0.6949	69.49%
skin sensitisation	-	0.8787	87.87%
Respiratory toxicity	+	0.6556	65.56%
Reproductive toxicity	+	0.8778	87.78%
Mitochondrial toxicity	+	0.6750	67.50%
Nephrotoxicity	+	0.5194	51.94%
Acute Oral Toxicity (c)	III	0.6412	64.12%
Estrogen receptor binding	+	0.5340	53.40%
Androgen receptor binding	+	0.5784	57.84%
Thyroid receptor binding	+	0.6113	61.13%
Glucocorticoid receptor binding	+	0.6455	64.55%
Aromatase binding	+	0.7129	71.29%
PPAR gamma	-	0.5171	51.71%
Honey bee toxicity	-	0.8596	85.96%
Biodegradation	-	0.8750	87.50%
Crustacea aquatic toxicity	-	0.6300	63.00%
Fish aquatic toxicity	+	0.9935	99.35%

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	97.97%	91.11%
CHEMBL253	P34972	Cannabinoid CB2 receptor	97.19%	97.25%
CHEMBL2581	P07339	Cathepsin D	90.51%	98.95%
CHEMBL3108638	O15164	Transcription intermediary factor 1-alpha	89.98%	95.56%
CHEMBL1994	P08235	Mineralocorticoid receptor	89.03%	100.00%
CHEMBL3137262	O60341	LSD1/CoREST complex	87.03%	97.09%
CHEMBL3038477	P67870	Casein kinase II alpha/beta	85.85%	99.23%
CHEMBL1937	Q92769	Histone deacetylase 2	83.46%	94.75%
CHEMBL4026	P40763	Signal transducer and activator of transcription 3	81.71%	82.69%

Plants that contains it

• Andrographis paniculata

Cross-Links

• PubChem: 44577191
• NPASS: NPC209355
• ChEMBL: CHEMBL466153
• LOTUS: LTS0237708
• wikiData: Q105300002