Anthcolorin A

Details

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Internal ID f837b620-8dbf-4d8b-a955-56239b0c860c
Taxonomy Organoheterocyclic compounds > Naphthopyrans
IUPAC Name (3R)-3-[[(3S,4aS,6aS,8S,10aR,10bS)-3-(2-hydroxypropan-2-yl)-6a,10b-dimethyl-7-methylidene-1,2,3,4a,5,6,8,9,10,10a-decahydrobenzo[f]chromen-8-yl]methyl]-1-(2-methylbut-3-en-2-yl)-3H-indol-2-one
SMILES (Canonical) CC12CCC(OC1CCC3(C2CCC(C3=C)CC4C5=CC=CC=C5N(C4=O)C(C)(C)C=C)C)C(C)(C)O
SMILES (Isomeric) C[C@@]12CC[C@H](O[C@H]1CC[C@]3([C@H]2CC[C@H](C3=C)C[C@@H]4C5=CC=CC=C5N(C4=O)C(C)(C)C=C)C)C(C)(C)O
InChI InChI=1S/C33H47NO3/c1-9-30(3,4)34-25-13-11-10-12-23(25)24(29(34)35)20-22-14-15-26-32(7,21(22)2)18-17-28-33(26,8)19-16-27(37-28)31(5,6)36/h9-13,22,24,26-28,36H,1-2,14-20H2,3-8H3/t22-,24+,26+,27-,28-,32+,33-/m0/s1
InChI Key QWTTYYHQARGNPV-NWWFIIQASA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C33H47NO3
Molecular Weight 505.70 g/mol
Exact Mass 505.35559436 g/mol
Topological Polar Surface Area (TPSA) 49.80 Ų
XlogP 6.40
Atomic LogP (AlogP) 7.18
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Anthcolorin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9812 98.12%
Caco-2 - 0.7295 72.95%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.5596 55.96%
OATP2B1 inhibitior - 0.8552 85.52%
OATP1B1 inhibitior + 0.8099 80.99%
OATP1B3 inhibitior + 0.9099 90.99%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior + 0.9873 98.73%
P-glycoprotein inhibitior + 0.7278 72.78%
P-glycoprotein substrate - 0.5862 58.62%
CYP3A4 substrate + 0.7067 70.67%
CYP2C9 substrate + 0.5839 58.39%
CYP2D6 substrate - 0.8363 83.63%
CYP3A4 inhibition + 0.6799 67.99%
CYP2C9 inhibition - 0.6453 64.53%
CYP2C19 inhibition - 0.5222 52.22%
CYP2D6 inhibition - 0.8200 82.00%
CYP1A2 inhibition - 0.6186 61.86%
CYP2C8 inhibition + 0.6384 63.84%
CYP inhibitory promiscuity + 0.5499 54.99%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.5831 58.31%
Eye corrosion - 0.9880 98.80%
Eye irritation - 0.9489 94.89%
Skin irritation - 0.7549 75.49%
Skin corrosion - 0.9005 90.05%
Ames mutagenesis - 0.5754 57.54%
Human Ether-a-go-go-Related Gene inhibition + 0.8072 80.72%
Micronuclear - 0.5000 50.00%
Hepatotoxicity - 0.5101 51.01%
skin sensitisation - 0.8253 82.53%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity + 0.5675 56.75%
Acute Oral Toxicity (c) III 0.6191 61.91%
Estrogen receptor binding + 0.7452 74.52%
Androgen receptor binding + 0.7493 74.93%
Thyroid receptor binding + 0.5934 59.34%
Glucocorticoid receptor binding + 0.7392 73.92%
Aromatase binding + 0.7070 70.70%
PPAR gamma + 0.6115 61.15%
Honey bee toxicity - 0.8460 84.60%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9919 99.19%

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 97.94% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.91% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.69% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.09% 86.33%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.32% 97.25%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.92% 89.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.17% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.89% 97.09%
CHEMBL5028 O14672 ADAM10 84.43% 97.50%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.40% 95.89%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.20% 94.45%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 84.09% 97.33%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 82.87% 90.93%
CHEMBL3524 P56524 Histone deacetylase 4 82.80% 92.97%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.06% 85.14%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.00% 100.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.77% 92.62%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 71713239
LOTUS LTS0135397
wikiData Q75057196