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5,6,11,14,17(R)-pentaacetoxy-5-(2-acetoxyacetoxy)-3-benzoyloxy-15-hydroxysegetan-9-one
- Family: Plantae - Euphorbiaceae
- Kingdom: Plantae
-
Class: Terpenoid
- Subclass: Diterpenoid
Canonical Smiles | CC(=O)O[C@@H]1[C@H]2[C@@H](Oc3ccccc3)[C@H](C[C@]2(O)C([C@@]2(C([C@@]1(OC(=O)C)C[C@@H]1[C@@H]2[C@@H](C(C1=O)(C)C)OC(=O)C)OC(=O)C)C)OC(=O)C)C |
---|---|
InChI | InChI=1S/C36H46O13/c1-17-15-35(43)26(27(17)48-23-13-11-10-12-14-23)30(45-19(3)38)36(49-22(6)41)16-24-25(29(44-18(2)37)33(7,8)28(24)42)34(9,31(35)46-20(4)39)32(36)47-21(5)40/h10-14,17,24-27,29-32,43H,15-16H2,1-9H3/t17-,24+,25+,26+,27-,29-,30+,31?,32?,34+,35+,36+/m0/s1 |
InChIKey | LINXZMLYWAEFLT-NPZYNBEJSA-N |
Formula | C36H46O13 |
HBA | 13 |
HBD | 1 |
MW | 686.75 |
Rotatable Bonds | 7 |
TPSA | 178.03 |
LogP | 3.11 |
Number Rings | 5 |
Number Aromatic Rings | 1 |
Heavy Atom Count | 49 |
Formal Charge | 0 |
Fraction CSP3 | 0.67 |
Exact Mass | 686.29 |
Number of Lipinski Rule Violations | 2 |
# | Species | Family | Kingdom | NCBI Taxonomy ID |
---|---|---|---|---|
1 | Euphorbia paralias | Euphorbiaceae | Plantae | 756629 |
Showing of synonyms
5,6,11,14,17(R)-pentaacetoxy-5-(2-acetoxyacetoxy)-3-benzoyloxy-15-hydroxysegetan-9-one
No compound-protein relationship available.
SMILES: O=C1CCC(C12)C3CC(C2)CC4C(C3)CCC4Oc5ccccc5
Level: 1
Mol. Weight: 686.75 g/mol
SMILES: O=C1CCC(C12)C3CC(C2)CC4C(C3)CCC4
Level: 0
Mol. Weight: 686.75 g/mol
SMILES: c1ccccc1
Level: 0
Mol. Weight: 686.75 g/mol
No bioactivities available.
Absorption
- Caco-2 (logPapp)
- -5.31
- Human Oral Bioavailability 20%
- Non-Bioavailable
- Human Intestinal Absorption
- Absorbed
- Madin-Darby Canine Kidney
- -4.39
- Human Oral Bioavailability 50%
- Non-Bioavailable
- P-Glycoprotein Inhibitor
- Inhibitor
- P-Glycoprotein Substrate
- Substrate
- Skin Permeability
- 63.15
Distribution
- Blood-Brain Barrier (CNS)
- -
- Blood-Brain Barrier
- Non-Penetrable
- Fraction Unbound (Human)
- 0.38
- Plasma Protein Binding
- 94.02
- Steady State Volume of Distribution
- -
Metabolism
- Breast Cancer Resistance Protein
- Non-Inhibitor
- CYP 1A2 Inhibitor
- Non-Inhibitor
- CYP 1A2 Substrate
- Non-Substrate
- CYP 2C19 Inhibitor
- Non-Inhibitor
- CYP 2C19 Substrate
- Non-Substrate
- CYP 2C9 Inhibitor
- Non-Inhibitor
- CYP 2C9 Substrate
- Non-Substrate
- CYP 2D6 Inhibitor
- Non-Inhibitor
- CYP 2D6 Substrate
- Non-Substrate
- CYP 3A4 Inhibitor
- Inhibitor
- CYP 3A4 Substrate
- Substrate
- OATP1B1
- Inhibitor
- OATP1B3
- Inhibitor
Excretion
- Clearance
- 7.86
- Organic Cation Transporter 2
- Non-Inhibitor
- Half-Life of Drug
- -
Toxicity
- AMES Mutagenesis
- Safe
- Avian
- Safe
- Bee
- Toxic
- Bioconcentration Factor
- 0.61
- Biodegradation
- Safe
- Carcinogenesis
- Safe
- Crustacean
- Safe
- Liver Injury I (DILI)
- Safe
- Eye Corrosion
- Safe
- Eye Irritation
- Safe
- Maximum Tolerated Dose
- 0.7
- Liver Injury II
- Toxic
- hERG Blockers
- Safe
- Daphnia Maga
- 8.33
- Micronucleos
- Toxic
- NR-AhR
- Safe
- NR-AR
- Toxic
- NR-AR-LBD
- Safe
- NR-Aromatase
- Safe
- NR-ER
- Safe
- NR-ER-LBD
- Safe
- NR-GR
- Toxic
- NR-PPAR-gamma
- Safe
- NR-TR
- Safe
- T. Pyriformis
- -119363.46
- Rat (Acute)
- 4.64
- Rat (Chronic Oral)
- 2.88
- Fathead Minnow
- 164.76
- Respiratory Disease
- Safe
- Skin Sensitisation
- Safe
- SR-ARE
- Safe
- SR-ATAD5
- Safe
- SR-HSE
- Safe
- SR-MMP
- Toxic
- SR-p53
- Safe
General Properties
- Boiling Point
- 8424.54
- Hydration Free Energy
- -2.92
- Log(D) at pH=7.4
- 2.06
- Log(P)
- 3.38
- Log S
- -4.81
- Log(Vapor Pressure)
- -297.92
- Melting Point
- 227.72
- pKa Acid
- 6.49
- pKa Basic
- -0.8
No predicted protein targets found for this compound.