Crassicausine

Details

Top
Internal ID 56d85791-204a-45c4-8d46-0f99fb7b7abe
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Aconitane-type diterpenoid alkaloids
IUPAC Name [11-ethyl-5-hydroxy-6,8,16,18-tetramethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 4-methoxybenzoate
SMILES (Canonical) CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=C(C=C7)OC)O)OC)OC)OC)OC)COC
SMILES (Isomeric) CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=C(C=C7)OC)O)OC)OC)OC)OC)COC
InChI InChI=1S/C34H49NO9/c1-8-35-17-31(18-38-2)14-13-22(40-4)34-21-15-32(37)23(41-5)16-33(43-7,25(28(34)35)26(42-6)27(31)34)24(21)29(32)44-30(36)19-9-11-20(39-3)12-10-19/h9-12,21-29,37H,8,13-18H2,1-7H3
InChI Key AFRMHVZQQVWATN-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C34H49NO9
Molecular Weight 615.80 g/mol
Exact Mass 615.34073214 g/mol
Topological Polar Surface Area (TPSA) 105.00 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.80
H-Bond Acceptor 10
H-Bond Donor 1
Rotatable Bonds 10

Synonyms

Top
Crassicausine
20-ethyl-13-hydroxy-1,6,8,16-tetramethoxy-4-(methoxymethyl)aconitan-14-yl 4-methoxybenzoate
DTXSID70911098

2D Structure

Top
2D Structure of Crassicausine

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9445 94.45%
Caco-2 - 0.7602 76.02%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Lysosomes 0.4370 43.70%
OATP2B1 inhibitior - 0.8594 85.94%
OATP1B1 inhibitior + 0.8935 89.35%
OATP1B3 inhibitior + 0.9361 93.61%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6599 65.99%
BSEP inhibitior + 0.9531 95.31%
P-glycoprotein inhibitior + 0.7473 74.73%
P-glycoprotein substrate + 0.6618 66.18%
CYP3A4 substrate + 0.7082 70.82%
CYP2C9 substrate - 0.8048 80.48%
CYP2D6 substrate - 0.6579 65.79%
CYP3A4 inhibition - 0.6081 60.81%
CYP2C9 inhibition - 0.8773 87.73%
CYP2C19 inhibition - 0.8721 87.21%
CYP2D6 inhibition - 0.8063 80.63%
CYP1A2 inhibition - 0.9281 92.81%
CYP2C8 inhibition + 0.7853 78.53%
CYP inhibitory promiscuity - 0.9251 92.51%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6025 60.25%
Eye corrosion - 0.9923 99.23%
Eye irritation - 0.9070 90.70%
Skin irritation - 0.7903 79.03%
Skin corrosion - 0.9480 94.80%
Ames mutagenesis - 0.6870 68.70%
Human Ether-a-go-go-Related Gene inhibition + 0.7958 79.58%
Micronuclear + 0.5100 51.00%
Hepatotoxicity - 0.5118 51.18%
skin sensitisation - 0.8714 87.14%
Respiratory toxicity + 0.8222 82.22%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.9375 93.75%
Nephrotoxicity - 0.8572 85.72%
Acute Oral Toxicity (c) III 0.4481 44.81%
Estrogen receptor binding + 0.8111 81.11%
Androgen receptor binding + 0.7286 72.86%
Thyroid receptor binding + 0.5681 56.81%
Glucocorticoid receptor binding - 0.4700 47.00%
Aromatase binding + 0.7342 73.42%
PPAR gamma + 0.7301 73.01%
Honey bee toxicity - 0.8683 86.83%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.8333 83.33%

Targets

Top

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 99.45% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.73% 97.25%
CHEMBL221 P23219 Cyclooxygenase-1 97.35% 90.17%
CHEMBL4208 P20618 Proteasome component C5 94.99% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.66% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 91.25% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.98% 97.09%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 89.09% 92.62%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.25% 93.99%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 87.24% 81.11%
CHEMBL340 P08684 Cytochrome P450 3A4 87.19% 91.19%
CHEMBL241 Q14432 Phosphodiesterase 3A 87.00% 92.94%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.75% 94.00%
CHEMBL2581 P07339 Cathepsin D 85.91% 98.95%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 85.65% 96.47%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.04% 96.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.46% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.06% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.13% 99.23%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 82.06% 91.07%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 81.79% 87.67%
CHEMBL3492 P49721 Proteasome Macropain subunit 81.57% 90.24%

Plants that contains it

Top
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.
Aconitum hemsleyanum

Cross-Links

Top
PubChem 184062
LOTUS LTS0243856
wikiData Q82881160