Punicalagin - Compound Card

Punicalagin

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Punicalagin

Structure
Zoomed Structure
  • Family: Plantae - Combretaceae
  • Kingdom: Plantae
  • Class: Tannin
Canonical Smiles O[C@@H]1O[C@@H]2COC(=O)c3cc(O)c(c(c3c3c(O)c(O)c4c5c3c(=O)oc3c(c(c(c6c(C(=O)O[C@H]2[C@H]2[C@H]1OC(=O)c1cc(O)c(c(c1c1c(C(=O)O2)cc(c(c1O)O)O)O)O)cc(O)c(c6O)O)c(c(=O)o4)c53)O)O)O)O
InChI InChI=1S/C48H28O30/c49-10-1-6-17(31(59)27(10)55)19-23-21-22-24(47(70)76-38(21)35(63)33(19)61)20(34(62)36(64)39(22)75-46(23)69)18-9(4-13(52)28(56)32(18)60)43(66)74-37-14(5-72-42(6)65)73-48(71)41-40(37)77-44(67)7-2-11(50)25(53)29(57)15(7)16-8(45(68)78-41)3-12(51)26(54)30(16)58/h1-4,14,37,40-41,48-64,71H,5H2/t14-,37-,40+,41-,48-/m1/s1
InChIKey ZJVUMAFASBFUBG-RILGRMFESA-N
Formula C48H28O30
HBA 30
HBD 17
MW 1084.72
Rotatable Bonds 0
TPSA 518.76
LogP 1.96
Number Rings 11
Number Aromatic Rings 8
Heavy Atom Count 78
Formal Charge 0
Fraction CSP3 0.12
Exact Mass 1084.07
Number of Lipinski Rule Violations 3
# Species Family Kingdom NCBI Taxonomy ID
1 Combretum molle Combretaceae Plantae 507414

Showing of synonyms

  • Asres K, Bucar F, et al. (2001). Investigations on antimycobacterial activity of some Ethiopian medicinal plants. Phytotherapy Research,2001,15(4),323-326. [View] [PubMed]
Pubchem: 16148440
Nmrshiftdb2: 60025349
Bindingdb: 50377922
CPRiL: 58623
Structure

SMILES: c1cc2oc(=O)c3c(ccc4oc5=O)c(cccc6)c6C(=O)OC(C7COC(=O)c(c8c1c5c2c34)cccc8)C9C(CO7)OC(=O)c1c(cccc1)c1c(C(=O)O9)cccc1

Level: 0

Mol. Weight: 1084.72 g/mol

No bioactivities available.

Absorption

Caco-2 (logPapp)
-6.09
Human Oral Bioavailability 20%
Non-Bioavailable
Human Intestinal Absorption
Non-Absorbed
Madin-Darby Canine Kidney
2934387.97
Human Oral Bioavailability 50%
Non-Bioavailable
P-Glycoprotein Inhibitor
Non-Inhibitor
P-Glycoprotein Substrate
Non-Substrate
Skin Permeability
383490739.74

Distribution

Blood-Brain Barrier (CNS)
-
Blood-Brain Barrier
Non-Penetrable
Fraction Unbound (Human)
0.53
Plasma Protein Binding
27.74
Steady State Volume of Distribution
-

Metabolism

Breast Cancer Resistance Protein
Inhibitor
CYP 1A2 Inhibitor
Non-Inhibitor
CYP 1A2 Substrate
Non-Substrate
CYP 2C19 Inhibitor
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
Inhibitor

Excretion

Clearance
10.43
Organic Cation Transporter 2
Inhibitor
Half-Life of Drug
-

Toxicity

AMES Mutagenesis
Safe
Avian
Toxic
Bee
Safe
Bioconcentration Factor
-8919115.32
Biodegradation
Safe
Carcinogenesis
Safe
Crustacean
Toxic
Liver Injury I (DILI)
Toxic
Eye Corrosion
Safe
Eye Irritation
Safe
Maximum Tolerated Dose
-3.16
Liver Injury II
Toxic
hERG Blockers
Toxic
Daphnia Maga
4.05
Micronucleos
Toxic
NR-AhR
Toxic
NR-AR
Safe
NR-AR-LBD
Toxic
NR-Aromatase
Safe
NR-ER
Safe
NR-ER-LBD
Safe
NR-GR
Safe
NR-PPAR-gamma
Safe
NR-TR
Safe
T. Pyriformis
-696017245146.72
Rat (Acute)
2.46
Rat (Chronic Oral)
1491.98
Fathead Minnow
878573471.51
Respiratory Disease
Toxic
Skin Sensitisation
Safe
SR-ARE
Toxic
SR-ATAD5
Safe
SR-HSE
Safe
SR-MMP
Toxic
SR-p53
Toxic

General Properties

Boiling Point
78282633400.15
Hydration Free Energy
-2.92
Log(D) at pH=7.4
-43516.65
Log(P)
-3.86
Log S
-7.0
Log(Vapor Pressure)
-2577807476.34
Melting Point
227.02
pKa Acid
-18783373.88
pKa Basic
-151077.26
Protein Name UniProt ID Entry Name Species #Pharmacophore Points Probability (0.7 ≤ Tversky Score ≤ 1.0)
Beta-secretase 1 P56817 BACE1_HUMAN Homo sapiens 3 0.7492
Beta-secretase 1 P56817 BACE1_HUMAN Homo sapiens 3 0.7492

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