Apigenin 8-C-glucoside - Compound Card

Apigenin 8-C-glucoside

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Apigenin 8-C-glucoside

Structure
Zoomed Structure
  • Family: Plantae - Neuradaceae
  • Kingdom: Plantae
  • Class: Flavonoid
    • Subclass: Flavonoid Glycoside
Canonical Smiles OC[C@H]1O[C@H]([C@@H]([C@H]([C@@H]1O)O)O[C@@H]1O[C@H](C)[C@H]([C@@H]([C@@H]1O)O)O)c1c(O)cc(c2c1oc(cc2=O)c1ccc(cc1)O)O
InChI InChI=1S/C27H30O14/c1-9-19(33)21(35)23(37)27(38-9)41-26-22(36)20(34)16(8-28)40-25(26)18-13(31)6-12(30)17-14(32)7-15(39-24(17)18)10-2-4-11(29)5-3-10/h2-7,9,16,19-23,25-31,33-37H,8H2,1H3/t9-,16-,19-,20-,21+,22+,23+,25+,26-,27+/m1/s1
InChIKey LYGPBZVKGHHTIE-NQQFNCMQSA-N
Formula C27H30O14
HBA 14
HBD 9
MW 578.52
Rotatable Bonds 5
TPSA 239.97
LogP -1.06
Number Rings 5
Number Aromatic Rings 3
Heavy Atom Count 41
Formal Charge 0
Fraction CSP3 0.44
Exact Mass 578.16
Number of Lipinski Rule Violations 3
# Species Family Kingdom NCBI Taxonomy ID
1 Borago officinalis Boraginaceae Plantae 13363
2 Neurada procumbens Neuradaceae Plantae 32215
3 Neurada procumbens Neuradaceae Plantae 32215

Showing of synonyms

  • Zemmouri H, Ammar S, et al. (2014). Chemical composition and antioxidant activity of Borago officinalis L. leaf extract growing in Algeria. Arabian Journal of Chemistry,2014,in press. [View]
  • Marzouk MM, Hussein SR, et al. (2014). Flavonoids from Neurada procumbens L. (Neuradaceae) in Egypt. Biochemical Systematics and Ecology,2014,57,67-68. [View]
  • Marzouk M, Hussein SR, et al. (2013). Flavonoids from Neurada procumbens L. (Neuradaceae) in Egypt. Planta Medica,2013,79-PI46. [View]
Pubchem: 20055288
Nmrshiftdb2: 60024623
CPRiL: 54730
Structure

SMILES: c1ccccc1-c(cc2=O)oc(c23)c(ccc3)C4C(CCCO4)OC5CCCCO5

Level: 3

Mol. Weight: 578.52 g/mol

Structure

SMILES: O=c1ccoc(c12)c(ccc2)C3C(CCCO3)OC4CCCCO4

Level: 2

Mol. Weight: 578.52 g/mol

Structure

SMILES: O1CCCCC1c(ccc2)c(c23)oc(cc3=O)-c4ccccc4

Level: 2

Mol. Weight: 578.52 g/mol

Structure

SMILES: O=c1ccoc(c12)c(ccc2)C3CCCCO3

Level: 1

Mol. Weight: 578.52 g/mol

Structure

SMILES: c1cccc(c12)oc(cc2=O)-c3ccccc3

Level: 1

Mol. Weight: 578.52 g/mol

Structure

SMILES: C1OCCCC1OC2CCCCO2

Level: 1

Mol. Weight: 578.52 g/mol

Structure

SMILES: c1cccc(c12)occc2=O

Level: 0

Mol. Weight: 578.52 g/mol

Structure

SMILES: C1CCOCC1

Level: 0

Mol. Weight: 578.52 g/mol

Structure

SMILES: c1ccccc1

Level: 0

Mol. Weight: 578.52 g/mol

No bioactivities available.

Absorption

Caco-2 (logPapp)
-6.37
Human Oral Bioavailability 20%
Non-Bioavailable
Human Intestinal Absorption
Non-Absorbed
Madin-Darby Canine Kidney
-5.730
Human Oral Bioavailability 50%
Non-Bioavailable
P-Glycoprotein Inhibitor
Non-Inhibitor
P-Glycoprotein Substrate
Substrate
Skin Permeability
4.95

Distribution

Blood-Brain Barrier (CNS)
-
Blood-Brain Barrier
Non-Penetrable
Fraction Unbound (Human)
0.760
Plasma Protein Binding
68.94
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
9.230
Organic Cation Transporter 2
Non-Inhibitor
Half-Life of Drug
-

Toxicity

AMES Mutagenesis
Toxic
Avian
Safe
Bee
Safe
Bioconcentration Factor
-3.150
Biodegradation
Safe
Carcinogenesis
Safe
Crustacean
Safe
Liver Injury I (DILI)
Safe
Eye Corrosion
Safe
Eye Irritation
Safe
Maximum Tolerated Dose
0.800
Liver Injury II
Toxic
hERG Blockers
Safe
Daphnia Maga
5.610
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
-5816.250
Rat (Acute)
2.470
Rat (Chronic Oral)
4.090
Fathead Minnow
13.290
Respiratory Disease
Safe
Skin Sensitisation
Safe
SR-ARE
Safe
SR-ATAD5
Safe
SR-HSE
Safe
SR-MMP
Safe
SR-p53
Toxic

General Properties

Boiling Point
546.320
Hydration Free Energy
-2.950
Log(D) at pH=7.4
-0.120
Log(P)
0.52
Log S
-4.15
Log(Vapor Pressure)
-11.35
Melting Point
177.38
pKa Acid
4.87
pKa Basic
8.53
Protein Name UniProt ID Entry Name Species #Pharmacophore Points Probability (0.7 ≤ Tversky Score ≤ 1.0)
Histone deacetylase 4 P56524 HDAC4_HUMAN Homo sapiens 3 0.8706
Histone deacetylase 4 P56524 HDAC4_HUMAN Homo sapiens 3 0.8706
Carbonic anhydrase 2 P00918 CAH2_HUMAN Homo sapiens 3 0.7620
Carbonic anhydrase 2 P00918 CAH2_HUMAN Homo sapiens 3 0.7620
Nuclear receptor subfamily 4immunitygroup A member 1 P22736 NR4A1_HUMAN Homo sapiens 3 0.7596
Nuclear receptor subfamily 4immunitygroup A member 1 P22736 NR4A1_HUMAN Homo sapiens 3 0.7596
Lactotransferrin P24627 TRFL_BOVIN Bos taurus 2 0.7488
Lactotransferrin P24627 TRFL_BOVIN Bos taurus 2 0.7488
Basic phospholipase A2 VRV-PL-VIIIa P59071 PA2B8_DABRR Daboia russelii 2 0.7082
Basic phospholipase A2 VRV-PL-VIIIa P59071 PA2B8_DABRR Daboia russelii 2 0.7082
Alpha amylase B8CZ54 B8CZ54_HALOH Halothermothrix orenii 3 0.7050
Alpha amylase B8CZ54 B8CZ54_HALOH Halothermothrix orenii 3 0.7050
Neuropilin-1 O14786 NRP1_HUMAN Homo sapiens 3 0.7033
Neuropilin-1 O14786 NRP1_HUMAN Homo sapiens 3 0.7033

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