Cannabin

Details

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Internal ID 481a23cb-c1a4-4875-b205-7eb6fdf952f9
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides > Flavonoid-3-O-glycosides
IUPAC Name 5-hydroxy-7-methoxy-2-phenyl-3-[(2S,5S)-3,4,5-trihydroxy-6-[[(2R,4S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one
SMILES (Canonical) CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC)C5=CC=CC=C5)O)O)O)O)O)O
SMILES (Isomeric) CC1[C@@H]([C@@H](C([C@@H](O1)OCC2[C@H](C(C([C@@H](O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC)C5=CC=CC=C5)O)O)O)O)O)O
InChI InChI=1S/C28H32O14/c1-11-18(30)21(33)23(35)27(39-11)38-10-16-19(31)22(34)24(36)28(41-16)42-26-20(32)17-14(29)8-13(37-2)9-15(17)40-25(26)12-6-4-3-5-7-12/h3-9,11,16,18-19,21-24,27-31,33-36H,10H2,1-2H3/t11?,16?,18-,19+,21-,22?,23?,24?,27+,28-/m0/s1
InChI Key PQRFZVPEJNZXRT-DHIFYZEUSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C28H32O14
Molecular Weight 592.50 g/mol
Exact Mass 592.17920569 g/mol
Topological Polar Surface Area (TPSA) 214.00 Ų
XlogP -0.20
Atomic LogP (AlogP) -0.80
H-Bond Acceptor 14
H-Bond Donor 7
Rotatable Bonds 7

Synonyms

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LMPK12111631

2D Structure

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2D Structure of Cannabin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.4777 47.77%
Caco-2 - 0.9054 90.54%
Blood Brain Barrier - 0.9250 92.50%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.6902 69.02%
OATP2B1 inhibitior - 0.8447 84.47%
OATP1B1 inhibitior + 0.8934 89.34%
OATP1B3 inhibitior + 0.9479 94.79%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.6263 62.63%
P-glycoprotein inhibitior - 0.5478 54.78%
P-glycoprotein substrate - 0.5355 53.55%
CYP3A4 substrate + 0.6099 60.99%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8527 85.27%
CYP3A4 inhibition - 0.8619 86.19%
CYP2C9 inhibition - 0.9071 90.71%
CYP2C19 inhibition - 0.9025 90.25%
CYP2D6 inhibition - 0.9231 92.31%
CYP1A2 inhibition - 0.9045 90.45%
CYP2C8 inhibition + 0.7640 76.40%
CYP inhibitory promiscuity - 0.6670 66.70%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6995 69.95%
Eye corrosion - 0.9891 98.91%
Eye irritation - 0.9159 91.59%
Skin irritation - 0.8249 82.49%
Skin corrosion - 0.9594 95.94%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3710 37.10%
Micronuclear + 0.7492 74.92%
Hepatotoxicity - 0.6198 61.98%
skin sensitisation - 0.9436 94.36%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity - 0.8885 88.85%
Acute Oral Toxicity (c) III 0.6904 69.04%
Estrogen receptor binding + 0.8212 82.12%
Androgen receptor binding + 0.6209 62.09%
Thyroid receptor binding + 0.5327 53.27%
Glucocorticoid receptor binding + 0.6368 63.68%
Aromatase binding + 0.6405 64.05%
PPAR gamma + 0.7266 72.66%
Honey bee toxicity - 0.8012 80.12%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.8477 84.77%

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 99.64% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.30% 85.14%
CHEMBL2581 P07339 Cathepsin D 97.76% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.06% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.39% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.67% 89.00%
CHEMBL1951 P21397 Monoamine oxidase A 94.66% 91.49%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.97% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 93.31% 99.15%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.37% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 90.79% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.58% 99.17%
CHEMBL3714130 P46095 G-protein coupled receptor 6 87.18% 97.36%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.17% 99.23%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.83% 95.50%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.60% 96.00%

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.
Datisca cannabina

Cross-Links

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PubChem 44258721
LOTUS LTS0263619
wikiData Q105213399