[(1S,3R,13R,14R,17S,18R,19R,20R,21S,22R,23R,24R)-19,21,22,24-tetraacetyloxy-20-(acetyloxymethyl)-14,25-dihydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-9-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-18-yl] furan-3-carboxylate

Details

• Internal ID: 50cbf447-e0d3-4602-80b8-b61dedbeb266
• Taxonomy: Lipids and lipid-like molecules > Prenol lipids > Terpene lactones
• IUPAC Name: [(1S,3R,13R,14R,17S,18R,19R,20R,21S,22R,23R,24R)-19,21,22,24-tetraacetyloxy-20-(acetyloxymethyl)-14,25-dihydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-9-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-18-yl] furan-3-carboxylate
• SMILES (Canonical): CC1C2=C(C=NC=C2)C(=O)OCC3(C4C(C(C5(C(C(C(C(C5(C4OC(=O)C)O3)(C)O)OC(=O)C1(C)O)OC(=O)C6=COC=C6)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C)C
• SMILES (Isomeric): C[C@@H]1C2=C(C=NC=C2)C(=O)OC[C@]3([C@@H]4[C@H]([C@H]([C@@]5([C@H]([C@H]([C@@H](C([C@]5([C@@H]4OC(=O)C)O3)(C)O)OC(=O)[C@]1(C)O)OC(=O)C6=COC=C6)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C)C
• InChI: InChI=1S/C41H47NO20/c1-18-25-10-12-42-14-26(25)35(49)55-16-37(7)27-28(56-20(3)44)32(58-22(5)46)40(17-54-19(2)43)33(59-23(6)47)29(60-34(48)24-11-13-53-15-24)31(61-36(50)38(18,8)51)39(9,52)41(40,62-37)30(27)57-21(4)45/h10-15,18,27-33,51-52H,16-17H2,1-9H3/t18-,27-,28-,29+,30-,31+,32-,33+,37+,38-,39?,40-,41+/m1/s1
• InChI Key: AVGYGFTXSUAKEM-RWRFEADFSA-N
• Popularity: 1 reference in papers

Physical and Chemical Properties

• Molecular Formula: C₄₁H₄₇NO₂₀
• Molecular Weight: 873.80 g/mol
• Exact Mass: 873.26914289 g/mol
• Topological Polar Surface Area (TPSA): 286.00 Ų
• XlogP: 0.20
• Atomic LogP (AlogP): 1.04
• H-Bond Acceptor: 21
• H-Bond Donor: 2
• Rotatable Bonds: 8

Synonyms

There are no found synonyms.

2D Structure

ADMET Properties (via admetSAR 2)

Target	Value	Probability (raw)	Probability (%)
Human Intestinal Absorption	+	0.7871	78.71%
Caco-2	-	0.8475	84.75%
Blood Brain Barrier	-	0.5750	57.50%
Human oral bioavailability	-	0.5429	54.29%
Subcellular localzation	Mitochondria	0.5919	59.19%
OATP2B1 inhibitior	-	0.7156	71.56%
OATP1B1 inhibitior	+	0.7819	78.19%
OATP1B3 inhibitior	+	0.9080	90.80%
MATE1 inhibitior	-	0.8800	88.00%
OCT2 inhibitior	-	0.8250	82.50%
BSEP inhibitior	+	0.9817	98.17%
P-glycoprotein inhibitior	+	0.8164	81.64%
P-glycoprotein substrate	+	0.6910	69.10%
CYP3A4 substrate	+	0.7212	72.12%
CYP2C9 substrate	-	0.6014	60.14%
CYP2D6 substrate	-	0.8857	88.57%
CYP3A4 inhibition	-	0.8279	82.79%
CYP2C9 inhibition	-	0.7820	78.20%
CYP2C19 inhibition	-	0.7450	74.50%
CYP2D6 inhibition	-	0.9358	93.58%
CYP1A2 inhibition	-	0.6585	65.85%
CYP2C8 inhibition	+	0.8314	83.14%
CYP inhibitory promiscuity	-	0.6104	61.04%
UGT catelyzed	-	0.5000	50.00%
Carcinogenicity (binary)	-	0.9700	97.00%
Carcinogenicity (trinary)	Non-required	0.5222	52.22%
Eye corrosion	-	0.9905	99.05%
Eye irritation	-	0.9023	90.23%
Skin irritation	-	0.8260	82.60%
Skin corrosion	-	0.9432	94.32%
Ames mutagenesis	-	0.5900	59.00%
Human Ether-a-go-go-Related Gene inhibition	+	0.6469	64.69%
Micronuclear	-	0.5800	58.00%
Hepatotoxicity	+	0.5782	57.82%
skin sensitisation	-	0.8629	86.29%
Respiratory toxicity	+	0.8111	81.11%
Reproductive toxicity	+	0.7889	78.89%
Mitochondrial toxicity	+	0.8625	86.25%
Nephrotoxicity	+	0.6840	68.40%
Acute Oral Toxicity (c)	III	0.4692	46.92%
Estrogen receptor binding	+	0.7980	79.80%
Androgen receptor binding	+	0.7413	74.13%
Thyroid receptor binding	+	0.6370	63.70%
Glucocorticoid receptor binding	+	0.7655	76.55%
Aromatase binding	+	0.6661	66.61%
PPAR gamma	+	0.7805	78.05%
Honey bee toxicity	-	0.7278	72.78%
Biodegradation	-	0.8750	87.50%
Crustacea aquatic toxicity	+	0.5203	52.03%
Fish aquatic toxicity	+	0.8973	89.73%

Targets

Proven Targets:

No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID	UniProt ID	Name	Probability	Model accuracy
CHEMBL4261	Q16665	Hypoxia-inducible factor 1 alpha	98.41%	85.14%
CHEMBL221	P23219	Cyclooxygenase-1	98.21%	90.17%
CHEMBL253	P34972	Cannabinoid CB2 receptor	97.99%	97.25%
CHEMBL1293249	Q13887	Kruppel-like factor 5	96.97%	86.33%
CHEMBL2996	Q05655	Protein kinase C delta	96.62%	97.79%
CHEMBL3251	P19838	Nuclear factor NF-kappa-B p105 subunit	96.60%	96.09%
CHEMBL1293277	O15118	Niemann-Pick C1 protein	95.45%	81.11%
CHEMBL2581	P07339	Cathepsin D	94.58%	98.95%
CHEMBL2039	P27338	Monoamine oxidase B	94.14%	92.51%
CHEMBL1951	P21397	Monoamine oxidase A	93.18%	91.49%
CHEMBL3038477	P67870	Casein kinase II alpha/beta	91.27%	99.23%
CHEMBL4481	P35228	Nitric oxide synthase, inducible	90.84%	94.80%
CHEMBL1907602	P06493	Cyclin-dependent kinase 1/cyclin B1	89.07%	91.24%
CHEMBL2007	P16234	Platelet-derived growth factor receptor alpha	88.91%	91.07%
CHEMBL5608	Q16288	NT-3 growth factor receptor	87.76%	95.89%
CHEMBL1806	P11388	DNA topoisomerase II alpha	86.85%	89.00%
CHEMBL3807	P17706	T-cell protein-tyrosine phosphatase	86.42%	93.00%
CHEMBL5028	O14672	ADAM10	85.65%	97.50%
CHEMBL5619	P27695	DNA-(apurinic or apyrimidinic site) lyase	85.47%	91.11%
CHEMBL1293267	Q9HC97	G-protein coupled receptor 35	84.66%	89.34%
CHEMBL4026	P40763	Signal transducer and activator of transcription 3	84.64%	82.69%
CHEMBL2635	P51452	Dual specificity protein phosphatase 3	84.09%	94.00%
CHEMBL5163	Q9NY46	Sodium channel protein type III alpha subunit	84.02%	96.90%
CHEMBL2094127	P06493	Cyclin-dependent kinase 1/cyclin B	83.90%	96.00%
CHEMBL4303	P08238	Heat shock protein HSP 90-beta	83.36%	96.77%
CHEMBL1293294	P51151	Ras-related protein Rab-9A	82.32%	87.67%
CHEMBL2107	P61073	C-X-C chemokine receptor type 4	82.21%	93.10%
CHEMBL1994	P08235	Mineralocorticoid receptor	80.85%	100.00%
CHEMBL1868	P17948	Vascular endothelial growth factor receptor 1	80.40%	96.47%

Plants that contains it

• Tripterygium wilfordii

Cross-Links

• PubChem: 477599
• LOTUS: LTS0058473
• wikiData: Q105100187