cinnamacrin-C

Details

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Internal ID fcafe660-3340-4394-80d3-a4a1f7c3211d
Taxonomy Organoheterocyclic compounds > Naphthofurans
IUPAC Name [(4R,5R,5aS,9aS)-4-[(4R,5R,5aS,9aS)-5-acetyloxy-6,6,9a-trimethyl-1-oxo-4,5,5a,7,8,9-hexahydro-3H-benzo[e][2]benzofuran-4-yl]-6,6,9a-trimethyl-1-oxo-4,5,5a,7,8,9-hexahydro-3H-benzo[e][2]benzofuran-5-yl] acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C34H46O8/c1-17(35)41-25-21(19-15-39-29(37)23(19)33(7)13-9-11-31(3,4)27(25)33)22-20-16-40-30(38)24(20)34(8)14-10-12-32(5,6)28(34)26(22)42-18(2)36/h21-22,25-28H,9-16H2,1-8H3/t21-,22-,25+,26+,27-,28-,33+,34+/m0/s1
InChI Key GOWXVGUUSAVPQS-OCWPFBGWSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C34H46O8
Molecular Weight 582.70 g/mol
Exact Mass 582.31926842 g/mol
Topological Polar Surface Area (TPSA) 105.00 Ų
XlogP 5.80
Atomic LogP (AlogP) 5.48
H-Bond Acceptor 8
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of cinnamacrin-C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9931 99.31%
Caco-2 - 0.6766 67.66%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.8377 83.77%
OATP2B1 inhibitior - 0.8615 86.15%
OATP1B1 inhibitior + 0.8949 89.49%
OATP1B3 inhibitior + 0.8548 85.48%
MATE1 inhibitior - 0.7000 70.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior + 0.9543 95.43%
P-glycoprotein inhibitior + 0.8087 80.87%
P-glycoprotein substrate - 0.8989 89.89%
CYP3A4 substrate + 0.5952 59.52%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9122 91.22%
CYP3A4 inhibition - 0.7882 78.82%
CYP2C9 inhibition - 0.6790 67.90%
CYP2C19 inhibition - 0.6974 69.74%
CYP2D6 inhibition - 0.8958 89.58%
CYP1A2 inhibition - 0.7144 71.44%
CYP2C8 inhibition - 0.8770 87.70%
CYP inhibitory promiscuity - 0.6849 68.49%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.4598 45.98%
Eye corrosion - 0.9857 98.57%
Eye irritation - 0.8630 86.30%
Skin irritation - 0.6769 67.69%
Skin corrosion - 0.9239 92.39%
Ames mutagenesis - 0.5637 56.37%
Human Ether-a-go-go-Related Gene inhibition - 0.5771 57.71%
Micronuclear - 0.6700 67.00%
Hepatotoxicity + 0.5803 58.03%
skin sensitisation - 0.7771 77.71%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity + 0.7447 74.47%
Acute Oral Toxicity (c) III 0.6639 66.39%
Estrogen receptor binding + 0.7678 76.78%
Androgen receptor binding + 0.6921 69.21%
Thyroid receptor binding + 0.5550 55.50%
Glucocorticoid receptor binding + 0.7737 77.37%
Aromatase binding + 0.6829 68.29%
PPAR gamma + 0.7160 71.60%
Honey bee toxicity - 0.8114 81.14%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6550 65.50%
Fish aquatic toxicity + 0.9966 99.66%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.38% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.23% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.90% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.03% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.63% 97.25%
CHEMBL2581 P07339 Cathepsin D 88.39% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.09% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.98% 86.33%
CHEMBL340 P08684 Cytochrome P450 3A4 85.10% 91.19%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.29% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.70% 89.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.96% 82.69%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 81.22% 81.11%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.92% 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.
Campomanesia lineatifolia
Cinnamosma macrocarpa

Cross-Links

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PubChem 16109831
NPASS NPC211988
LOTUS LTS0138328
wikiData Q105237192