Argeloside F - Compound Card

Argeloside F

Select a section from the left sidebar

Argeloside F

Family: Plantae - Apocynaceae
Kingdom: Plantae
Class: Steroid
- Subclass: Pregnane Glycoside

Canonical Smiles	COC1CC(OC(C1OC1CC(OC)C(C(O1)C)OC1OC(C)C(C(C1O)OC)OC1OC(CO)C(C(C1O)O)O)C)OC1C(O)CC(OC1C)O[C@H]1CC[C@]2(C(=CC[C@@H]3[C@@H]2CC[C@]2([C@@]43O[C@H]3[C@@H]2[C@](O4)(C)OC3)C)C1)C
InChI	InChI=1S/C54H86O22/c1-23-43(31(56)18-36(65-23)69-28-13-15-51(5)27(17-28)11-12-30-29(51)14-16-52(6)48-35-22-64-53(48,7)76-54(30,52)75-35)71-37-19-32(61-8)44(24(2)66-37)72-38-20-33(62-9)45(25(3)67-38)73-50-42(60)47(63-10)46(26(4)68-50)74-49-41(59)40(58)39(57)34(21-55)70-49/h11,23-26,28-50,55-60H,12-22H2,1-10H3/t23?,24?,25?,26?,28-,29-,30+,31?,32?,33?,34?,35+,36?,37?,38?,39?,40?,41?,42?,43?,44?,45?,46?,47?,48-,49?,50?,51-,52+,53+,54-/m0/s1
InChIKey	CYZMTPXCWHTCPU-KVZMHDEHSA-N
Formula	C₅₄H₈₆O₂₂
HBA	22
HBD	6
MW	1087.26
Rotatable Bonds	14
TPSA	269.06
LogP	1.67
Number Rings	11
Number Aromatic Rings	0
Heavy Atom Count	76
Formal Charge	0
Fraction CSP3	0.96
Exact Mass	1086.56
Number of Lipinski Rule Violations	3

#	Species	Family	Kingdom	NCBI Taxonomy ID
1	Solenostemma argel	Apocynaceae	Plantae	219273

Showing of synonyms

Perrone A, Plaza A, et al. (2006). 14,15-Secopregnane derivatives from the leaves of Solenostemma argel. Journal of Natural Products,2006,69(1),50-54. [View] [PubMed]

Pubchem: 11251763

Chembl: CHEMBL450701

CPRiL: 430539

SMILES: O1C2OCC(O3)C2C(C134)CCC5C4CC=C6C5CCC(C6)OC(OC7)CCC7OC(OC8)CCC8OC(OC9)CCC9OC(OC1)CCC1OC1CCCCO1

Level: 5

Mol. Weight: 1087.26 g/mol

SMILES: O1C2OCC(O3)C2C(C134)CCC5C4CC=C6C5CCC(C6)OC(OC7)CCC7OC(OC8)CCC8OC(OC9)CCC9OC1CCCCO1

Level: 4

Mol. Weight: 1087.26 g/mol

SMILES: O1CCCCC1OC2CCC(OC2)OC3CCC(OC3)OC4CCC(OC4)OC5CCCOC5

Level: 4

Mol. Weight: 1087.26 g/mol

SMILES: O1C2OCC(O3)C2C(C134)CCC5C4CC=C6C5CCC(C6)OC(OC7)CCC7OC(OC8)CCC8OC9CCCCO9

Level: 3

Mol. Weight: 1087.26 g/mol

SMILES: C1OCCCC1OC(OC2)CCC2OC(OC3)CCC3OC4CCCCO4

Level: 3

Mol. Weight: 1087.26 g/mol

SMILES: O1C2OCC(O3)C2C(C134)CCC5C4CC=C6C5CCC(C6)OC(OC7)CCC7OC8CCCCO8

Level: 2

Mol. Weight: 1087.26 g/mol

SMILES: O1CCCCC1OC2CCC(OC2)OC3CCCOC3

Level: 2

Mol. Weight: 1087.26 g/mol

SMILES: O1C2OCC(O3)C2C(C134)CCC5C4CC=C6C5CCC(C6)OC7CCCCO7

Level: 1

Mol. Weight: 1087.26 g/mol

SMILES: C1OCCCC1OC2CCCCO2

Level: 1

Mol. Weight: 1087.26 g/mol

SMILES: O1C2OCC(O3)C2C(C134)CCC5C4CC=C6C5CCCC6

Level: 0

Mol. Weight: 1087.26 g/mol

SMILES: C1CCOCC1

Level: 0

Mol. Weight: 1087.26 g/mol

Inhibition of tnf-alpha release

Absorption

Caco-2 (logPapp): -6.0
Human Oral Bioavailability 20%: Bioavailable
Human Intestinal Absorption: Absorbed
Madin-Darby Canine Kidney: 1605912.550
Human Oral Bioavailability 50%: Non-Bioavailable
P-Glycoprotein Inhibitor: Non-Inhibitor
P-Glycoprotein Substrate: Substrate
Skin Permeability: 209874666.5

Distribution

Blood-Brain Barrier (CNS): -
Blood-Brain Barrier: Non-Penetrable
Fraction Unbound (Human): 0.640
Plasma Protein Binding: 55.76
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: Substrate
OATP1B1: Non-Inhibitor
OATP1B3: Non-Inhibitor

Excretion

Clearance: 3.230
Organic Cation Transporter 2: Non-Inhibitor
Half-Life of Drug: -

Toxicity

General Properties

Boiling Point: 42842074112.770
Hydration Free Energy: -2.920
Log(D) at pH=7.4: -23801.500
Log(P): 0.53
Log S: -3.68
Log(Vapor Pressure): -1410767661.61
Melting Point: 120.76
pKa Acid: -10279580.11
pKa Basic: -82685.67

Protein Name	UniProt ID	Entry Name	Species	#Pharmacophore Points	Probability (0.7 ≤ Tversky Score ≤ 1.0)
Nuclear receptor ROR-alpha	P35398	RORA_HUMAN	Homo sapiens	5	0.7098
Nuclear receptor ROR-alpha	P35398	RORA_HUMAN	Homo sapiens	5	0.7098