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16alpha-hydroxy-5,6-dehydrocalotropin
- Family: Plantae - Apocynaceae
- Kingdom: Plantae
-
Class: Glycoside
- Subclass: Cardenolide Glycoside
| Canonical Smiles | O=C[C@]12C[C@H]3O[C@@]4(O)[C@@H](O)C[C@H](O[C@H]4O[C@@H]3CC1=CC[C@@H]1[C@@H]2CC[C@]2([C@]1(O)C[C@H]([C@@H]2C1=CC(=O)OC1)O)C)C |
|---|---|
| InChI | InChI=1S/C29H38O10/c1-14-7-22(32)29(35)25(37-14)38-20-9-16-3-4-18-17(27(16,13-30)11-21(20)39-29)5-6-26(2)24(15-8-23(33)36-12-15)19(31)10-28(18,26)34/h3,8,13-14,17-22,24-25,31-32,34-35H,4-7,9-12H2,1-2H3/t14-,17+,18-,19-,20-,21-,22+,24+,25+,26-,27-,28+,29+/m1/s1 |
| InChIKey | BCHAIGZJQCUIHZ-KGTCOYFRSA-N |
| Formula | C29H38O10 |
| HBA | 10 |
| HBD | 4 |
| MW | 546.61 |
| Rotatable Bonds | 2 |
| TPSA | 151.98 |
| LogP | 0.89 |
| Number Rings | 7 |
| Number Aromatic Rings | 0 |
| Heavy Atom Count | 39 |
| Formal Charge | 0 |
| Fraction CSP3 | 0.79 |
| Exact Mass | 546.25 |
| Number of Lipinski Rule Violations | 1 |
| # | Species | Family | Kingdom | NCBI Taxonomy ID |
|---|---|---|---|---|
| 1 | Gomphocarpus sinaicus | Apocynaceae | Plantae | 2291033 |
Showing of synonyms
16alpha-hydroxy-5,6-dehydrocalotropin
- El-Askary H, Holzl J, et al. (1995). Cardenolide glycosides from Gomphocarpus sinaicus. Phytochemistry,1995,38(4),943-946. [View]
No compound-protein relationship available.
SMILES: C1OC(=O)C=C1C2CCC(C23)C4C(CC3)C5C(=CC4)CC6C(C5)OC7C(O6)OCCC7
Level: 1
Mol. Weight: 546.61 g/mol
SMILES: C1CCC(C12)CCC3C2CC=C4C3CC5C(C4)OC6C(O5)CCCO6
Level: 0
Mol. Weight: 546.61 g/mol
SMILES: O=C1C=CCO1
Level: 0
Mol. Weight: 546.61 g/mol
No bioactivities available.
Absorption
- Caco-2 (logPapp)
- -5.47
- Human Oral Bioavailability 20%
- Non-Bioavailable
- Human Intestinal Absorption
- Absorbed
- Madin-Darby Canine Kidney
- -4.94
- Human Oral Bioavailability 50%
- Bioavailable
- P-Glycoprotein Inhibitor
- Non-Inhibitor
- P-Glycoprotein Substrate
- Substrate
- Skin Permeability
- 0.78
Distribution
- Blood-Brain Barrier (CNS)
- -
- Blood-Brain Barrier
- Penetrable
- Fraction Unbound (Human)
- 0.57
- Plasma Protein Binding
- 55.52
- 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
- Non-Inhibitor
- CYP 3A4 Substrate
- Non-Substrate
- OATP1B1
- Non-Inhibitor
- OATP1B3
- Non-Inhibitor
Excretion
- Clearance
- 2.76
- Organic Cation Transporter 2
- Non-Inhibitor
- Half-Life of Drug
- -
Toxicity
- AMES Mutagenesis
- Toxic
- Avian
- Safe
- Bee
- Toxic
- Bioconcentration Factor
- -3.18
- Biodegradation
- Safe
- Carcinogenesis
- Safe
- Crustacean
- Safe
- Liver Injury I (DILI)
- Safe
- Eye Corrosion
- Safe
- Eye Irritation
- Safe
- Maximum Tolerated Dose
- -1.28
- Liver Injury II
- Toxic
- hERG Blockers
- Toxic
- Daphnia Maga
- 6.88
- Micronucleos
- Toxic
- NR-AhR
- Safe
- NR-AR
- Safe
- NR-AR-LBD
- Toxic
- NR-Aromatase
- Toxic
- NR-ER
- Toxic
- NR-ER-LBD
- Safe
- NR-GR
- Toxic
- NR-PPAR-gamma
- Safe
- NR-TR
- Toxic
- T. Pyriformis
- -4110.65
- Rat (Acute)
- 4.96
- Rat (Chronic Oral)
- 1.9
- Fathead Minnow
- 12.76
- Respiratory Disease
- Safe
- Skin Sensitisation
- Safe
- SR-ARE
- Safe
- SR-ATAD5
- Toxic
- SR-HSE
- Safe
- SR-MMP
- Toxic
- SR-p53
- Safe
General Properties
- Boiling Point
- 421.92
- Hydration Free Energy
- -2.92
- Log(D) at pH=7.4
- 1.98
- Log(P)
- 0.09
- Log S
- -3.28
- Log(Vapor Pressure)
- -10.51
- Melting Point
- 258.0
- pKa Acid
- 5.4
- pKa Basic
- 4.69
No predicted protein targets found for this compound.