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Beta-amyrin
- Family: Plantae - Moraceae
- Kingdom: Plantae
-
Class: Terpenoid
- Subclass: Triterpenoid
Canonical Smiles | C[C@@]12CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)O)C)C)[C@@H]1CC(CC2)(C)C)C |
---|---|
InChI | InChI=1S/C30H50O/c1-25(2)15-16-27(5)17-18-29(7)20(21(27)19-25)9-10-23-28(6)13-12-24(31)26(3,4)22(28)11-14-30(23,29)8/h9,21-24,31H,10-19H2,1-8H3/t21-,22-,23+,24-,27+,28-,29+,30+/m0/s1 |
InChIKey | JFSHUTJDVKUMTJ-QHPUVITPSA-N |
Formula | C30H50O |
HBA | 1 |
HBD | 1 |
MW | 426.73 |
Rotatable Bonds | 0 |
TPSA | 20.23 |
LogP | 8.17 |
Number Rings | 5 |
Number Aromatic Rings | 0 |
Heavy Atom Count | 31 |
Formal Charge | 0 |
Fraction CSP3 | 0.93 |
Exact Mass | 426.39 |
Number of Lipinski Rule Violations | 1 |
# | Species | Family | Kingdom | NCBI Taxonomy ID |
---|---|---|---|---|
1 | Periploca laevigata | Apocynaceae | Plantae | 413294 |
2 | Solenostemma argel | Apocynaceae | Plantae | 219273 |
3 | Trichodesma africanum | Boraginaceae | Plantae | 379304 |
4 | Centaurea africana | Asteraceae | Plantae | 2950952 |
5 | Sonchus macrocarpus | Asteraceae | Plantae | 2984305 |
6 | Commiphora kua | Burseraceae | Plantae | 246356 |
7 | Commiphora confusa | Burseraceae | Plantae | 43868 |
8 | Escinops ellenbeckii | Asteraceae | Plantae | — |
9 | Vernonia auriculifera | Asteraceae | Plantae | 3032568 |
10 | Vernonia auriculifera | Asteraceae | Plantae | 3032568 |
11 | Platycelyphium voënse | Leguminosae/Fabaceae | Plantae | 149667 |
12 | Ficus carica | Moraceae | Plantae | 3494 |
13 | Ficus sycomorus | Moraceae | Plantae | — |
Showing of synonyms
Beta-amyrin
559-70-6
Beta-Amyrenol
UNII-KM8353IPSO
3beta-hydroxyolean-12-ene
KM8353IPSO
CHEBI:10352
AMYRIN, BETA-
EINECS 209-204-6
NSC 527971
(3beta)-olean-12-en-3-ol
Olean-12-en-3-ol, (3beta)-
NSC-527971
209-204-6
Amyrin
Olean-12-en-3beta-ol
B-Amyrin
Olean-12-en-3-ol, (3b)-
(3S,4aR,6aR,6bS,8aR,12aR,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-ol
CHEMBL455098
-amyrin
Beta.-Amyrenol
Beta -Amyrin
Beta.-Amyrin
MFCD00017381
I(2)-Amyrin
.BETA.-AMYRIN [MI]
SCHEMBL377754
Beta-Amyrin, analytical standard
JFSHUTJDVKUMTJ-QHPUVITPSA-N
DTXSID201025005
EX-A6672
HY-N2922
(3-.beta.)-Olean-12-en-3-ol
BDBM50241955
AKOS032962060
FA16227
LMPR0106150015
(3S,4aR,6aR,6bS,8aR,12aR,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-icosahydropicen-3-ol
BS-32560
12-Oleanen-3-beta-ol
Olean-12-en-3b-ol
CS-0023527
NS00076600
C08616
D85202
Q27108621
(3S,4aR,5R,6aR,6bR,8S,8aR,12aR,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-eicosahydro-picen-3-ol
- Seghiri R, Boumaza O, et al. (2009). A flavonoid with cytotoxic activity and other constituents from Centaurea africana. Phytochemistry Letters,2009,2(3),114-118. [View]
- Hymete A, Rohloff J, et al. (2005). Acetylenic thiophenes from the roots of Escinops ellenbeckii from Ethiopia. Natural Product Research,2005,19(8),755-761. [View] [PubMed]
- Omar M, Defeo J, et al. (1983). Chemical and toxicity studies of Trichodesma africanum L.. Journal of Natural Products,1983,46(2),153-156. [View] [PubMed]
- Abu-Mustafa E, H. El-Tawil B, et al. (1963). Constituents of Local Plants-IV. Ficus Carica L., F. Sycomorus L. And F. Salicifolia L. Leaves. Phytochemistry, 1963, 3(6), 701-703. [View]
- Manguro LO, Ugi I, et al. (2003). Dammarane triterpenes of Commiphora confusa resin. Chemical and Pharmaceutical Bulletin,2003,51(5),483-486. [View] [PubMed]
- Gumula I, Heydenreic M, et al. (2012). Four isoflavanones from the stem bark of Platycelphium voënse.. Phytochemistry Letters,2012,5(1),150–154. [View] [PubMed]
- Manguro LO, Ugi I, et al. (2003). Further bisabolenes and dammarane triterpenes of Commiphora kua resin.. Chemical and Pharmaceutical Bulletin,2003,51(5),479-482. [View] [PubMed]
- Askri M, Mighri Z, et al. (1989). Medicinal plants of Tunisia. the structure of periplocadiol, a new elemane-type sesquiterpene isolated from the roots of Periploca laevigata. Journal of Natural Products,1989,52(4),792-796. [View]
- Hassan HA, Hamed AI, et al. (2001). Pregnene derivatives from Solenostemma argel leaves. Phytochemistry,2001,57(4),507-511. [View] [PubMed]
- Kiplimo JJ, Koorbanally NA. (2012). The phytochemistry and biological activity of secondary metabolites from Kenyan Vernonia and Vepris species. PhD Thesis, University of Kwazulu-Natal, South Africa,2012. [View] [PubMed]
- Kiplimo JJ, Koorbanally NA, et al. (2011). Triterpenoids from Vernonia auriculifera Hiern exhibit antimicrobial activity. African Journal of Pharmacy and Pharmacology,2011,5(8),1150-1156. [View] [PubMed]
- Mahmoud Z, El-Masry S, et al. (1983). Two eudesmanolides from Sonchus macrocarpus. Phytochemistry,1983,22(5),1290-1291. [View]
Pubchem:
73145
Cas:
559-70-6
Gnps:
CCMSLIB00000579938
Zinc:
ZINC000003978270
Kegg Ligand:
C08616
Chebi:
10352
Nmrshiftdb2:
60018438
Metabolights:
MTBLC10352
Chembl:
CHEMBL455098
Bindingdb:
50241955
CPRiL:
61879
SMILES: C1CCCC2C1CCC(C2=3)C4C(CC3)C5C(CC4)CCCC5
Level: 0
Mol. Weight: 426.73 g/mol
Antibacterial
Absorption
- Caco-2 (logPapp)
- -4.81
- Human Oral Bioavailability 20%
- Bioavailable
- Human Intestinal Absorption
- Absorbed
- Madin-Darby Canine Kidney
- -4.42
- Human Oral Bioavailability 50%
- Bioavailable
- P-Glycoprotein Inhibitor
- Non-Inhibitor
- P-Glycoprotein Substrate
- Non-Substrate
- Skin Permeability
- -2.68
Distribution
- Blood-Brain Barrier (CNS)
- -
- Blood-Brain Barrier
- Penetrable
- Fraction Unbound (Human)
- 1.65
- Plasma Protein Binding
- 84.81
- 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
- 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
- 11.97
- Organic Cation Transporter 2
- Non-Inhibitor
- Half-Life of Drug
- -
Toxicity
- AMES Mutagenesis
- Safe
- Avian
- Safe
- Bee
- Toxic
- Bioconcentration Factor
- 1.02
- Biodegradation
- Safe
- Carcinogenesis
- Safe
- Crustacean
- Toxic
- Liver Injury I (DILI)
- Safe
- Eye Corrosion
- Safe
- Eye Irritation
- Safe
- Maximum Tolerated Dose
- 1.62
- Liver Injury II
- Safe
- hERG Blockers
- Toxic
- Daphnia Maga
- 5.9
- Micronucleos
- Safe
- NR-AhR
- Safe
- NR-AR
- Toxic
- NR-AR-LBD
- Safe
- NR-Aromatase
- Safe
- NR-ER
- Safe
- NR-ER-LBD
- Safe
- NR-GR
- Safe
- NR-PPAR-gamma
- Safe
- NR-TR
- Toxic
- T. Pyriformis
- -31.75
- Rat (Acute)
- 2.32
- Rat (Chronic Oral)
- 1.29
- Fathead Minnow
- 3.92
- Respiratory Disease
- Toxic
- Skin Sensitisation
- Toxic
- SR-ARE
- Safe
- SR-ATAD5
- Safe
- SR-HSE
- Safe
- SR-MMP
- Safe
- SR-p53
- Safe
General Properties
- Boiling Point
- 397.78
- Hydration Free Energy
- -3.77
- Log(D) at pH=7.4
- 7.4
- Log(P)
- 8.55
- Log S
- -7.26
- Log(Vapor Pressure)
- -7.48
- Melting Point
- 237.5
- pKa Acid
- 13.09
- pKa Basic
- 8.06