Claulansine D

Details

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Internal ID 89c73326-342c-4365-ba19-27f7d44ac809
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Carbazoles
IUPAC Name (1S)-1-[(1S)-1,2-dihydroxy-2-methylpropyl]-10-methoxy-1,9-dihydrofuro[3,4-b]carbazol-3-one
SMILES (Canonical) CC(C)(C(C1C2=C(C=C3C4=CC=CC=C4NC3=C2OC)C(=O)O1)O)O
SMILES (Isomeric) CC(C)([C@H]([C@@H]1C2=C(C=C3C4=CC=CC=C4NC3=C2OC)C(=O)O1)O)O
InChI InChI=1S/C19H19NO5/c1-19(2,23)17(21)16-13-11(18(22)25-16)8-10-9-6-4-5-7-12(9)20-14(10)15(13)24-3/h4-8,16-17,20-21,23H,1-3H3/t16-,17-/m0/s1
InChI Key KDKOLSIYWLCHCE-IRXDYDNUSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H19NO5
Molecular Weight 341.40 g/mol
Exact Mass 341.12632271 g/mol
Topological Polar Surface Area (TPSA) 91.80 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.67
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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CHEMBL2035833

2D Structure

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2D Structure of Claulansine D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9672 96.72%
Caco-2 - 0.5129 51.29%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.5308 53.08%
OATP2B1 inhibitior - 0.8620 86.20%
OATP1B1 inhibitior + 0.8783 87.83%
OATP1B3 inhibitior + 0.8946 89.46%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.8020 80.20%
P-glycoprotein inhibitior - 0.5772 57.72%
P-glycoprotein substrate - 0.6713 67.13%
CYP3A4 substrate + 0.6302 63.02%
CYP2C9 substrate - 0.8060 80.60%
CYP2D6 substrate - 0.8354 83.54%
CYP3A4 inhibition - 0.7654 76.54%
CYP2C9 inhibition - 0.7956 79.56%
CYP2C19 inhibition - 0.6773 67.73%
CYP2D6 inhibition - 0.7976 79.76%
CYP1A2 inhibition + 0.5112 51.12%
CYP2C8 inhibition - 0.5958 59.58%
CYP inhibitory promiscuity + 0.5551 55.51%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.4413 44.13%
Eye corrosion - 0.9924 99.24%
Eye irritation - 0.8389 83.89%
Skin irritation - 0.8416 84.16%
Skin corrosion - 0.9583 95.83%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6544 65.44%
Micronuclear + 0.7600 76.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.8493 84.93%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity - 0.9167 91.67%
Acute Oral Toxicity (c) III 0.5116 51.16%
Estrogen receptor binding + 0.8377 83.77%
Androgen receptor binding + 0.6068 60.68%
Thyroid receptor binding + 0.7891 78.91%
Glucocorticoid receptor binding + 0.8551 85.51%
Aromatase binding + 0.7496 74.96%
PPAR gamma + 0.7211 72.11%
Honey bee toxicity - 0.7563 75.63%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.8076 80.76%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.72% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.23% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.63% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.09% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.56% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.66% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.85% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.76% 99.23%
CHEMBL2535 P11166 Glucose transporter 90.66% 98.75%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 90.53% 93.03%
CHEMBL213 P08588 Beta-1 adrenergic receptor 89.96% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 88.10% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.82% 94.45%
CHEMBL1907 P15144 Aminopeptidase N 86.83% 93.31%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.38% 94.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.95% 92.62%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 83.67% 95.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.88% 99.17%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.50% 97.14%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 81.64% 94.23%
CHEMBL1951 P21397 Monoamine oxidase A 81.30% 91.49%

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.
Clausena lansium

Cross-Links

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PubChem 57409548
NPASS NPC166401