Harrisonin

Details

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Internal ID 1bd6d578-0575-42f0-8250-a6347bc77ebc
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids > Limonoids
IUPAC Name methyl (Z)-3-[(1R,2R,4S,7S,8S,11R,12R,13R,17S)-7-(furan-3-yl)-13,17-dihydroxy-1,8,12,15,15-pentamethyl-5,14-dioxo-3,6,16-trioxapentacyclo[9.6.0.02,4.02,8.013,17]heptadecan-12-yl]prop-2-enoate
SMILES (Canonical) CC1(C(=O)C2(C(C3CCC4(C(OC(=O)C5C4(C3(C2(O1)O)C)O5)C6=COC=C6)C)(C)C=CC(=O)OC)O)C
SMILES (Isomeric) C[C@@]12CC[C@@H]3[C@@]([C@]4(C(=O)C(O[C@]4([C@]3([C@@]15[C@H](O5)C(=O)O[C@H]2C6=COC=C6)C)O)(C)C)O)(C)/C=C\C(=O)OC
InChI InChI=1S/C27H32O10/c1-21(2)20(30)25(31)22(3,11-8-16(28)33-6)15-7-10-23(4)17(14-9-12-34-13-14)35-19(29)18-26(23,36-18)24(15,5)27(25,32)37-21/h8-9,11-13,15,17-18,31-32H,7,10H2,1-6H3/b11-8-/t15-,17+,18-,22-,23+,24-,25+,26-,27+/m1/s1
InChI Key DYNIRWNERRSOEV-HPGFDZHLSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C27H32O10
Molecular Weight 516.50 g/mol
Exact Mass 516.19954721 g/mol
Topological Polar Surface Area (TPSA) 145.00 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.98
H-Bond Acceptor 10
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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CHEBI:5627
62026-30-6
C08766
CHEMBL2398516
DTXSID901098352
Q27106831
Methyl (2Z)-3-[(3S,3aS,5aR,6R,6aR,9aS,9bR,9cR,10aS)-3-(3-furanyl)dodecahydro-6a,9a-dihydroxy-3a,6,8,8,9b-pentamethyl-1,7-dioxo-3H-furo[3',2':4,5]cyclopent[1,2-f]oxireno[d]-2-benzopyran-6-yl]-2-propenoate
methyl (Z)-3-[(1R,2R,4S,7S,8S,11R,12R,13R,17S)-7-(furan-3-yl)-13,17-dihydroxy-1,8,12,15,15-pentamethyl-5,14-dioxo-3,6,16-trioxapentacyclo[9.6.0.02,4.02,8.013,17]heptadecan-12-yl]prop-2-enoate

2D Structure

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2D Structure of Harrisonin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9049 90.49%
Caco-2 - 0.7332 73.32%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.6929 69.29%
OATP2B1 inhibitior - 0.8584 85.84%
OATP1B1 inhibitior - 0.3486 34.86%
OATP1B3 inhibitior + 0.8656 86.56%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.8230 82.30%
P-glycoprotein inhibitior + 0.7059 70.59%
P-glycoprotein substrate - 0.5574 55.74%
CYP3A4 substrate + 0.7126 71.26%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8741 87.41%
CYP3A4 inhibition + 0.7081 70.81%
CYP2C9 inhibition - 0.7097 70.97%
CYP2C19 inhibition - 0.7077 70.77%
CYP2D6 inhibition - 0.8966 89.66%
CYP1A2 inhibition - 0.8106 81.06%
CYP2C8 inhibition + 0.6903 69.03%
CYP inhibitory promiscuity - 0.8069 80.69%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Danger 0.4369 43.69%
Eye corrosion - 0.9871 98.71%
Eye irritation - 0.9143 91.43%
Skin irritation - 0.7039 70.39%
Skin corrosion - 0.8896 88.96%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6510 65.10%
Micronuclear - 0.5800 58.00%
Hepatotoxicity - 0.5106 51.06%
skin sensitisation - 0.8263 82.63%
Respiratory toxicity + 0.7778 77.78%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity + 0.7126 71.26%
Acute Oral Toxicity (c) I 0.3754 37.54%
Estrogen receptor binding + 0.8073 80.73%
Androgen receptor binding + 0.7849 78.49%
Thyroid receptor binding + 0.6757 67.57%
Glucocorticoid receptor binding + 0.7891 78.91%
Aromatase binding + 0.7709 77.09%
PPAR gamma + 0.6061 60.61%
Honey bee toxicity - 0.7849 78.49%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9850 98.50%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL4040 P28482 MAP kinase ERK2 99.49% 83.82%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.79% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.44% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.24% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.63% 86.33%
CHEMBL221 P23219 Cyclooxygenase-1 89.11% 90.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.52% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.10% 97.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.05% 89.00%
CHEMBL340 P08684 Cytochrome P450 3A4 85.32% 91.19%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.66% 95.56%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.47% 92.62%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.14% 100.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.88% 94.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Harrisonia abyssinica
Harrisonia perforata

Cross-Links

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PubChem 5281308
LOTUS LTS0140133
wikiData Q27106831