Camellisin A

Details

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Internal ID 0fa87e5e-d830-45a6-a73f-4cb49d10d23e
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (3S,4R,4aR,6aR,6bS,8aR,10R,11S,12R,12aS,14S,14aR,14bS)-3,10,13,14-tetrahydroxy-4,6a,6b,8a,11,12,14b-heptamethyl-9-oxo-1,2,3,4a,5,6,7,8,10,11,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid
SMILES (Canonical) CC1C(C(C(=O)C2(C1C3=C(C(C4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C(=O)O)O)C)O)O)C)O)C
SMILES (Isomeric) C[C@H]1[C@@H]([C@H](C(=O)[C@]2([C@@H]1C3=C([C@H]([C@@H]4[C@]5(CC[C@@H]([C@]([C@@H]5CC[C@]4([C@@]3(CC2)C)C)(C)C(=O)O)O)C)O)O)C)O)C
InChI InChI=1S/C30H46O7/c1-14-15(2)20(32)24(35)27(4)12-13-28(5)19(18(14)27)21(33)22(34)23-26(3)10-9-17(31)30(7,25(36)37)16(26)8-11-29(23,28)6/h14-18,20,22-23,31-34H,8-13H2,1-7H3,(H,36,37)/t14-,15-,16+,17-,18-,20+,22+,23+,26-,27+,28+,29+,30+/m0/s1
InChI Key LINFZXYZNSSYGY-VDYGIRSDSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C30H46O7
Molecular Weight 518.70 g/mol
Exact Mass 518.32435380 g/mol
Topological Polar Surface Area (TPSA) 135.00 Ų
XlogP 4.10
Atomic LogP (AlogP) 4.10
H-Bond Acceptor 6
H-Bond Donor 5
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Camellisin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9614 96.14%
Caco-2 - 0.7139 71.39%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.8093 80.93%
OATP2B1 inhibitior - 0.7136 71.36%
OATP1B1 inhibitior + 0.8459 84.59%
OATP1B3 inhibitior - 0.3942 39.42%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6092 60.92%
BSEP inhibitior - 0.7062 70.62%
P-glycoprotein inhibitior - 0.6337 63.37%
P-glycoprotein substrate - 0.5977 59.77%
CYP3A4 substrate + 0.6902 69.02%
CYP2C9 substrate - 0.8233 82.33%
CYP2D6 substrate - 0.8461 84.61%
CYP3A4 inhibition - 0.8238 82.38%
CYP2C9 inhibition - 0.8964 89.64%
CYP2C19 inhibition - 0.8743 87.43%
CYP2D6 inhibition - 0.9533 95.33%
CYP1A2 inhibition - 0.8876 88.76%
CYP2C8 inhibition - 0.6334 63.34%
CYP inhibitory promiscuity - 0.9833 98.33%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6499 64.99%
Eye corrosion - 0.9928 99.28%
Eye irritation - 0.9083 90.83%
Skin irritation + 0.6472 64.72%
Skin corrosion - 0.9329 93.29%
Ames mutagenesis - 0.7754 77.54%
Human Ether-a-go-go-Related Gene inhibition - 0.5353 53.53%
Micronuclear - 0.7700 77.00%
Hepatotoxicity - 0.5834 58.34%
skin sensitisation - 0.7774 77.74%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.8875 88.75%
Nephrotoxicity - 0.5545 55.45%
Acute Oral Toxicity (c) IV 0.3126 31.26%
Estrogen receptor binding + 0.7091 70.91%
Androgen receptor binding + 0.7364 73.64%
Thyroid receptor binding + 0.5429 54.29%
Glucocorticoid receptor binding + 0.6859 68.59%
Aromatase binding + 0.6725 67.25%
PPAR gamma + 0.5841 58.41%
Honey bee toxicity - 0.8357 83.57%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9937 99.37%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.27% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.48% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.30% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.80% 94.45%
CHEMBL221 P23219 Cyclooxygenase-1 86.37% 90.17%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.02% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.70% 99.23%
CHEMBL340 P08684 Cytochrome P450 3A4 85.33% 91.19%
CHEMBL2581 P07339 Cathepsin D 83.23% 98.95%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.58% 93.04%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.14% 82.69%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.89% 95.89%

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.
Camellia sinensis

Cross-Links

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PubChem 46850615
LOTUS LTS0109812
wikiData Q105152294