(4aR,4bR,7S,10aR)-7-[(1S)-1,2-dihydroxyethyl]-1,1,4a,7-tetramethyl-2,3,4b,5,6,8,10,10a-octahydrophenanthren-4-one

Details

• Internal ID: 5af526fa-60c8-4d94-8525-91183b22a0c2
• Taxonomy: Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
• IUPAC Name: (4aR,4bR,7S,10aR)-7-[(1S)-1,2-dihydroxyethyl]-1,1,4a,7-tetramethyl-2,3,4b,5,6,8,10,10a-octahydrophenanthren-4-one
• InChI: InChI=1S/C20H32O3/c1-18(2)9-8-16(22)20(4)14-7-10-19(3,17(23)12-21)11-13(14)5-6-15(18)20/h5,14-15,17,21,23H,6-12H2,1-4H3/t14-,15-,17-,19+,20+/m1/s1
• InChI Key: HJNUJRDGRMXBAR-CTZQRVGRSA-N
• Popularity: 2 references in papers

Physical and Chemical Properties

• Molecular Formula: C₂₀H₃₂O₃
• Molecular Weight: 320.50 g/mol
• Exact Mass: 320.23514488 g/mol
• Topological Polar Surface Area (TPSA): 57.50 Ų
• XlogP: 2.70
• Atomic LogP (AlogP): 3.49
• H-Bond Acceptor: 3
• H-Bond Donor: 2
• Rotatable Bonds: 2

Synonyms

There are no found synonyms.

2D Structure

ADMET Properties (via admetSAR 2)

Target	Value	Probability (raw)	Probability (%)
Human Intestinal Absorption	+	0.9947	99.47%
Caco-2	+	0.7401	74.01%
Blood Brain Barrier	+	0.6385	63.85%
Human oral bioavailability	-	0.5857	58.57%
Subcellular localzation	Mitochondria	0.8789	87.89%
OATP2B1 inhibitior	-	0.8597	85.97%
OATP1B1 inhibitior	+	0.9155	91.55%
OATP1B3 inhibitior	+	0.9426	94.26%
MATE1 inhibitior	-	1.0000	100.00%
OCT2 inhibitior	+	0.5352	53.52%
BSEP inhibitior	+	0.6590	65.90%
P-glycoprotein inhibitior	-	0.7651	76.51%
P-glycoprotein substrate	-	0.7909	79.09%
CYP3A4 substrate	+	0.5911	59.11%
CYP2C9 substrate	-	0.8326	83.26%
CYP2D6 substrate	-	0.8034	80.34%
CYP3A4 inhibition	-	0.7961	79.61%
CYP2C9 inhibition	-	0.8174	81.74%
CYP2C19 inhibition	-	0.8645	86.45%
CYP2D6 inhibition	-	0.9323	93.23%
CYP1A2 inhibition	-	0.8916	89.16%
CYP2C8 inhibition	-	0.8513	85.13%
CYP inhibitory promiscuity	-	0.8936	89.36%
UGT catelyzed	-	0.6000	60.00%
Carcinogenicity (binary)	-	0.9600	96.00%
Carcinogenicity (trinary)	Non-required	0.6880	68.80%
Eye corrosion	-	0.9920	99.20%
Eye irritation	-	0.9387	93.87%
Skin irritation	-	0.5827	58.27%
Skin corrosion	-	0.9629	96.29%
Ames mutagenesis	-	0.6500	65.00%
Human Ether-a-go-go-Related Gene inhibition	-	0.4545	45.45%
Micronuclear	-	0.9000	90.00%
Hepatotoxicity	-	0.6788	67.88%
skin sensitisation	-	0.7558	75.58%
Respiratory toxicity	+	0.6889	68.89%
Reproductive toxicity	+	0.8889	88.89%
Mitochondrial toxicity	+	0.7500	75.00%
Nephrotoxicity	-	0.6495	64.95%
Acute Oral Toxicity (c)	III	0.7430	74.30%
Estrogen receptor binding	+	0.7810	78.10%
Androgen receptor binding	+	0.5515	55.15%
Thyroid receptor binding	+	0.7092	70.92%
Glucocorticoid receptor binding	+	0.8701	87.01%
Aromatase binding	+	0.6215	62.15%
PPAR gamma	+	0.6849	68.49%
Honey bee toxicity	-	0.8936	89.36%
Biodegradation	-	0.7750	77.50%
Crustacea aquatic toxicity	-	0.7500	75.00%
Fish aquatic toxicity	+	0.9798	97.98%

Targets

Proven Targets:

No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID	UniProt ID	Name	Probability	Model accuracy
CHEMBL253	P34972	Cannabinoid CB2 receptor	97.27%	97.25%
CHEMBL5619	P27695	DNA-(apurinic or apyrimidinic site) lyase	96.53%	91.11%
CHEMBL3251	P19838	Nuclear factor NF-kappa-B p105 subunit	96.03%	96.09%
CHEMBL4040	P28482	MAP kinase ERK2	96.01%	83.82%
CHEMBL2581	P07339	Cathepsin D	93.64%	98.95%
CHEMBL3137262	O60341	LSD1/CoREST complex	90.32%	97.09%
CHEMBL1937	Q92769	Histone deacetylase 2	89.37%	94.75%
CHEMBL1994	P08235	Mineralocorticoid receptor	86.41%	100.00%
CHEMBL4203	Q9HAZ1	Dual specificity protein kinase CLK4	86.00%	94.45%
CHEMBL3108638	O15164	Transcription intermediary factor 1-alpha	85.82%	95.56%
CHEMBL3038477	P67870	Casein kinase II alpha/beta	83.66%	99.23%
CHEMBL3351	Q13085	Acetyl-CoA carboxylase 1	83.44%	93.04%
CHEMBL4026	P40763	Signal transducer and activator of transcription 3	80.57%	82.69%
CHEMBL5845	P23415	Glycine receptor subunit alpha-1	80.43%	90.71%
CHEMBL1907600	Q00535	Cyclin-dependent kinase 5/CDK5 activator 1	80.34%	93.03%

Plants that contains it

• Rhizophora apiculata

Cross-Links

• PubChem: 53496372
• LOTUS: LTS0225952
• wikiData: Q105029349