3beta,4alpha,10alpha-trihydroxy-1beta,2beta-epoxy-8alpha-valeryloxy-11,13-dehydroguaia-6alpha,12-olide - Compound Card

3beta,4alpha,10alpha-trihydroxy-1beta,2beta-epoxy-8alpha-valeryloxy-11,13-dehydroguaia-6alpha,12-olide

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3beta,4alpha,10alpha-trihydroxy-1beta,2beta-epoxy-8alpha-valeryloxy-11,13-dehydroguaia-6alpha,12-olide

Structure
Zoomed Structure
  • Family: Plantae - Asteraceae
  • Kingdom: Plantae
  • Class: Terpenoid
    • Subclass: Sesquiterpene Lactone
Canonical Smiles CC(CC(=O)O[C@H]1C[C@@](C)(O)[C@@]23[C@@H]([C@@H]4[C@@H]1[C@H](C)C(=O)O4)[C@]([C@H]([C@H]3O2)O)(C)O)C
InChI InChI=1S/C20H30O8/c1-8(2)6-11(21)26-10-7-18(4,24)20-14(13-12(10)9(3)17(23)27-13)19(5,25)15(22)16(20)28-20/h8-10,12-16,22,24-25H,6-7H2,1-5H3/t9-,10-,12+,13-,14-,15-,16+,18+,19-,20-/m0/s1
InChIKey PWSUYVPATIVWCL-TYURWWHESA-N
Formula C20H30O8
HBA 8
HBD 3
MW 398.45
Rotatable Bonds 3
TPSA 125.82
LogP 0.16
Number Rings 4
Number Aromatic Rings 0
Heavy Atom Count 28
Formal Charge 0
Fraction CSP3 0.9
Exact Mass 398.19
Number of Lipinski Rule Violations 0
# Species Family Kingdom NCBI Taxonomy ID
1 Otanthus maritimus Asteraceae Plantae 1155244

Showing of synonyms

  • Jakupovic J, Boeker R, et al. (1988). Highly oxygenated guaianolides from Otanthus maritimus. Phytochemistry,1988,27(4),1135-1140. [View]
Pubchem: 14021404
Nmrshiftdb2: 60056763

No compound-protein relationship available.

Structure

SMILES: C123C(O3)CCC1C4C(CC(=O)O4)CCC2

Level: 0

Mol. Weight: 398.45 g/mol

No bioactivities available.

Absorption

Caco-2 (logPapp)
-5.19
Human Oral Bioavailability 20%
Non-Bioavailable
Human Intestinal Absorption
Absorbed
Madin-Darby Canine Kidney
-4.78
Human Oral Bioavailability 50%
Bioavailable
P-Glycoprotein Inhibitor
Non-Inhibitor
P-Glycoprotein Substrate
Non-Substrate
Skin Permeability
-2.24

Distribution

Blood-Brain Barrier (CNS)
-
Blood-Brain Barrier
Penetrable
Fraction Unbound (Human)
0.31
Plasma Protein Binding
36.54
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
Non-Inhibitor
OATP1B3
Non-Inhibitor

Excretion

Clearance
10.06
Organic Cation Transporter 2
Non-Inhibitor
Half-Life of Drug
-

Toxicity

AMES Mutagenesis
Safe
Avian
Safe
Bee
Toxic
Bioconcentration Factor
-0.08
Biodegradation
Safe
Carcinogenesis
Safe
Crustacean
Safe
Liver Injury I (DILI)
Safe
Eye Corrosion
Safe
Eye Irritation
Safe
Maximum Tolerated Dose
0.3
Liver Injury II
Safe
hERG Blockers
Safe
Daphnia Maga
6.14
Micronucleos
Toxic
NR-AhR
Safe
NR-AR
Safe
NR-AR-LBD
Safe
NR-Aromatase
Safe
NR-ER
Safe
NR-ER-LBD
Safe
NR-GR
Safe
NR-PPAR-gamma
Safe
NR-TR
Safe
T. Pyriformis
-8.86
Rat (Acute)
5.17
Rat (Chronic Oral)
2.35
Fathead Minnow
3.8
Respiratory Disease
Safe
Skin Sensitisation
Safe
SR-ARE
Safe
SR-ATAD5
Safe
SR-HSE
Safe
SR-MMP
Safe
SR-p53
Safe

General Properties

Boiling Point
402.81
Hydration Free Energy
-8.85
Log(D) at pH=7.4
0.28
Log(P)
0.63
Log S
-2.38
Log(Vapor Pressure)
-8.24
Melting Point
141.23
pKa Acid
5.19
pKa Basic
3.39
Protein Name UniProt ID Entry Name Species #Pharmacophore Points Probability (0.7 ≤ Tversky Score ≤ 1.0)
Sarcoplasmic/endoplasmic reticulum calcium ATPase 1 P04191 AT2A1_RABIT Oryctolagus cuniculus 3 0.8137
Sarcoplasmic/endoplasmic reticulum calcium ATPase 1 P04191 AT2A1_RABIT Oryctolagus cuniculus 3 0.8137
Lysozyme C II P11941 LYSC2_ONCMY Oncorhynchus mykiss 3 0.7763
Lysozyme C II P11941 LYSC2_ONCMY Oncorhynchus mykiss 3 0.7763
Cytochrome P450 Q93H81 Q93H81_STRAX Streptomyces avermitilis 3 0.7427
Cytochrome P450 Q93H81 Q93H81_STRAX Streptomyces avermitilis 3 0.7427
Lactoylglutathione lyase Q9CPU0 LGUL_MOUSE Mus musculus 2 0.7266
Lactoylglutathione lyase Q9CPU0 LGUL_MOUSE Mus musculus 2 0.7266

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