Nervonin B

Details

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Internal ID 2869bbce-9f84-43b0-bcef-95dd98bdc87d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Kaurane diterpenoids
IUPAC Name [(1R,2R,3R,4R,6S,8S,9S,10S,11S,13S)-2,3-diacetyloxy-6,8-dihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate
SMILES (Canonical) CC(=O)OC1CC2CC3(C1C4(C(CC(C(C4C(C3OC(=O)C)OC(=O)C)(C)C)O)O)C)C(=O)C2=C
SMILES (Isomeric) CC(=O)O[C@H]1C[C@@H]2C[C@]3([C@@H]1[C@@]4([C@H](C[C@@H](C([C@H]4[C@H]([C@@H]3OC(=O)C)OC(=O)C)(C)C)O)O)C)C(=O)C2=C
InChI InChI=1S/C26H36O9/c1-11-15-8-16(33-12(2)27)20-25(7)18(31)9-17(30)24(5,6)21(25)19(34-13(3)28)23(35-14(4)29)26(20,10-15)22(11)32/h15-21,23,30-31H,1,8-10H2,2-7H3/t15-,16+,17+,18+,19-,20+,21-,23+,25+,26+/m1/s1
InChI Key NOZXMJPFKFLMJK-LYVLPCRDSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C26H36O9
Molecular Weight 492.60 g/mol
Exact Mass 492.23593272 g/mol
Topological Polar Surface Area (TPSA) 136.00 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.72
H-Bond Acceptor 9
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Nervonin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9826 98.26%
Caco-2 - 0.6548 65.48%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.6311 63.11%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8878 88.78%
OATP1B3 inhibitior + 0.8657 86.57%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.4888 48.88%
P-glycoprotein inhibitior + 0.6201 62.01%
P-glycoprotein substrate - 0.6687 66.87%
CYP3A4 substrate + 0.6611 66.11%
CYP2C9 substrate - 0.7947 79.47%
CYP2D6 substrate - 0.8731 87.31%
CYP3A4 inhibition - 0.7441 74.41%
CYP2C9 inhibition - 0.8308 83.08%
CYP2C19 inhibition - 0.8365 83.65%
CYP2D6 inhibition - 0.9232 92.32%
CYP1A2 inhibition - 0.8792 87.92%
CYP2C8 inhibition - 0.6919 69.19%
CYP inhibitory promiscuity - 0.9173 91.73%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6186 61.86%
Eye corrosion - 0.9891 98.91%
Eye irritation - 0.8896 88.96%
Skin irritation - 0.5441 54.41%
Skin corrosion - 0.9319 93.19%
Ames mutagenesis - 0.6042 60.42%
Human Ether-a-go-go-Related Gene inhibition - 0.4558 45.58%
Micronuclear - 0.5900 59.00%
Hepatotoxicity + 0.5575 55.75%
skin sensitisation - 0.6009 60.09%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity + 0.6961 69.61%
Acute Oral Toxicity (c) I 0.4224 42.24%
Estrogen receptor binding + 0.7824 78.24%
Androgen receptor binding + 0.6334 63.34%
Thyroid receptor binding + 0.5465 54.65%
Glucocorticoid receptor binding + 0.6893 68.93%
Aromatase binding + 0.5913 59.13%
PPAR gamma + 0.6846 68.46%
Honey bee toxicity - 0.6964 69.64%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9928 99.28%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.10% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.51% 94.45%
CHEMBL340 P08684 Cytochrome P450 3A4 90.79% 91.19%
CHEMBL2581 P07339 Cathepsin D 90.58% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.57% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.93% 85.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.33% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.66% 95.56%
CHEMBL259 P32245 Melanocortin receptor 4 82.53% 95.38%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.29% 99.23%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.31% 91.07%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.97% 95.50%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.39% 93.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 80.15% 82.69%

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.
Isodon nervosus

Cross-Links

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PubChem 24862639
NPASS NPC200957
ChEMBL CHEMBL468383
LOTUS LTS0187698
wikiData Q105182923