Marmin

Details

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Internal ID 36b72615-1caf-4166-a162-b30701178f60
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 7-[(E,6R)-6,7-dihydroxy-3,7-dimethyloct-2-enoxy]chromen-2-one
SMILES (Canonical) CC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)CCC(C(C)(C)O)O
SMILES (Isomeric) C/C(=C\COC1=CC2=C(C=C1)C=CC(=O)O2)/CC[C@H](C(C)(C)O)O
InChI InChI=1S/C19H24O5/c1-13(4-8-17(20)19(2,3)22)10-11-23-15-7-5-14-6-9-18(21)24-16(14)12-15/h5-7,9-10,12,17,20,22H,4,8,11H2,1-3H3/b13-10+/t17-/m1/s1
InChI Key QYYKWTUUCOTGNS-JIIJFUIFSA-N
Popularity 12 references in papers

Physical and Chemical Properties

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Molecular Formula C19H24O5
Molecular Weight 332.40 g/mol
Exact Mass 332.16237386 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 3.00
Atomic LogP (AlogP) 3.03
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 7

Synonyms

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14957-38-1
R-(+)-Marmin
CID 6450230
7-(6',7'-Dihydroxygeranyloxy)coumarin
7-[(E,6R)-6,7-dihydroxy-3,7-dimethyloct-2-enoxy]chromen-2-one
(R-(E))-7-((6,7-Dihydroxy-3,7-dimethyl-2-octenyl)oxy)-2H-1-benzopyran-2-one
HMS2198E18
(+)-Marmin
MLS002472929
CHEMBL1078441
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Marmin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9596 95.96%
Caco-2 + 0.5984 59.84%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.8470 84.70%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8613 86.13%
OATP1B3 inhibitior + 0.8371 83.71%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7818 78.18%
BSEP inhibitior + 0.8394 83.94%
P-glycoprotein inhibitior - 0.6335 63.35%
P-glycoprotein substrate - 0.7761 77.61%
CYP3A4 substrate + 0.5560 55.60%
CYP2C9 substrate - 0.8170 81.70%
CYP2D6 substrate - 0.8130 81.30%
CYP3A4 inhibition - 0.7896 78.96%
CYP2C9 inhibition - 0.6449 64.49%
CYP2C19 inhibition + 0.5605 56.05%
CYP2D6 inhibition - 0.8469 84.69%
CYP1A2 inhibition + 0.7729 77.29%
CYP2C8 inhibition - 0.7328 73.28%
CYP inhibitory promiscuity - 0.8693 86.93%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6734 67.34%
Eye corrosion - 0.9924 99.24%
Eye irritation - 0.9489 94.89%
Skin irritation - 0.7277 72.77%
Skin corrosion - 0.9570 95.70%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8624 86.24%
Micronuclear - 0.7800 78.00%
Hepatotoxicity - 0.5833 58.33%
skin sensitisation - 0.8302 83.02%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.7330 73.30%
Acute Oral Toxicity (c) III 0.4565 45.65%
Estrogen receptor binding + 0.8665 86.65%
Androgen receptor binding + 0.7991 79.91%
Thyroid receptor binding + 0.6652 66.52%
Glucocorticoid receptor binding + 0.7731 77.31%
Aromatase binding + 0.8001 80.01%
PPAR gamma + 0.8806 88.06%
Honey bee toxicity - 0.8540 85.40%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.9955 99.55%

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
CHEMBL2039 P27338 Monoamine oxidase B 99.80% 92.51%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.35% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.17% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 97.07% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.61% 99.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.59% 94.00%
CHEMBL1951 P21397 Monoamine oxidase A 85.07% 91.49%
CHEMBL1907 P15144 Aminopeptidase N 84.99% 93.31%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.91% 86.33%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 84.15% 89.34%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.34% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.22% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.20% 96.00%
CHEMBL4208 P20618 Proteasome component C5 81.87% 90.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.74% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.65% 99.23%

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.
Aegle marmelos
Citrus × aurantium
Citrus medica
Citrus trifoliata
Rosa transmorrisonensis
Solidago drummondii

Cross-Links

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PubChem 6450230
NPASS NPC113098
ChEMBL CHEMBL1078441
LOTUS LTS0019953
wikiData Q104389968