Strobopinin

Details

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Internal ID f6946444-354d-460e-b8e3-bc7b877b30df
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavans > Flavanones
IUPAC Name (2S)-5,7-dihydroxy-6-methyl-2-phenyl-2,3-dihydrochromen-4-one
SMILES (Canonical) CC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O
SMILES (Isomeric) CC1=C(C2=C(C=C1O)O[C@@H](CC2=O)C3=CC=CC=C3)O
InChI InChI=1S/C16H14O4/c1-9-11(17)7-14-15(16(9)19)12(18)8-13(20-14)10-5-3-2-4-6-10/h2-7,13,17,19H,8H2,1H3/t13-/m0/s1
InChI Key INBPQAJYHSJVRY-ZDUSSCGKSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C16H14O4
Molecular Weight 270.28 g/mol
Exact Mass 270.08920892 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.11
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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CHEBI:9292
11023-71-5
491-66-7
(-)-strobopinin
C09939
CHEMBL227611
SCHEMBL4740200
DTXSID60911547
LMPK12140187
Q27108348
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Strobopinin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9463 94.63%
Caco-2 - 0.5148 51.48%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.7969 79.69%
OATP2B1 inhibitior - 0.8662 86.62%
OATP1B1 inhibitior + 0.9281 92.81%
OATP1B3 inhibitior + 0.9395 93.95%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8099 80.99%
P-glycoprotein inhibitior - 0.8084 80.84%
P-glycoprotein substrate - 0.9468 94.68%
CYP3A4 substrate - 0.5423 54.23%
CYP2C9 substrate - 0.7974 79.74%
CYP2D6 substrate - 0.7747 77.47%
CYP3A4 inhibition + 0.8322 83.22%
CYP2C9 inhibition + 0.9091 90.91%
CYP2C19 inhibition + 0.8751 87.51%
CYP2D6 inhibition - 0.7485 74.85%
CYP1A2 inhibition + 0.9317 93.17%
CYP2C8 inhibition - 0.6401 64.01%
CYP inhibitory promiscuity + 0.7479 74.79%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6160 61.60%
Eye corrosion - 0.9931 99.31%
Eye irritation + 0.7862 78.62%
Skin irritation - 0.5602 56.02%
Skin corrosion - 0.9139 91.39%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5920 59.20%
Micronuclear + 0.8459 84.59%
Hepatotoxicity - 0.5092 50.92%
skin sensitisation - 0.8910 89.10%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.6475 64.75%
Acute Oral Toxicity (c) I 0.3194 31.94%
Estrogen receptor binding + 0.6668 66.68%
Androgen receptor binding + 0.6358 63.58%
Thyroid receptor binding + 0.5678 56.78%
Glucocorticoid receptor binding + 0.6539 65.39%
Aromatase binding - 0.4934 49.34%
PPAR gamma + 0.7622 76.22%
Honey bee toxicity - 0.9459 94.59%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.8635 86.35%

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 98.31% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.36% 95.56%
CHEMBL2581 P07339 Cathepsin D 95.37% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.67% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.08% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.49% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.44% 85.14%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.56% 99.15%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 83.88% 85.11%
CHEMBL3401 O75469 Pregnane X receptor 83.20% 94.73%

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.
Adina trichotoma
Afraegle paniculata
Ajuga genevensis
Alnus cordata
Alnus sieboldiana
Aloe deltoideodonta
Ammodendron karelinii
Anacyclus pyrethrum
Artemisia argyi
Aster tataricus
Astragalus glycyphyllos
Athrixia elata
Bauhinia purpurea
Boronia pinnata
Brachylaena perrieri
Buglossoides arvensis
Cassinia subtropica
Centaurea cheiranthifolia
Cladanthus arabicus
Cleistanthus indochinensis
Cleome spinosa
Colchicum arenarium
Cratoxylum formosum subsp. pruniflorum
Crinum jagus
Crinum latifolium
Cuscuta australis
Cyrtomium falcatum
Daphnandra johnsonii
Dianella revoluta
Diplotropis ferruginea
Elettaria cardamomum
Elymus repens
Erythrina burttii
Eucalyptus viminalis
Euphrasia regelii
Glochidion sphaerogynum
Gyrothyra underwoodiana
Hemionitis aschenborniana
Hippeastrum aulicum
Hortonia angustifolia
Jacobaea erucifolia subsp. argunensis
Julbernardia globiflora
Kokoona ochracea
Laggera crispata
Lamprolobium fruticosum
Leitneria floridana
Lepechinia caulescens
Leptospermum scoparium
Machilus obovatifolia
Maprounea guianensis
Medicosma fareana
Mentha longifolia subsp. longifolia
Mentha pulegium
Mikania grazielae
Miliusa balansae
Mimusops laurifolia
Myrrhis odorata
Othonna macrophylla
Pentachondra pumila
Peritassa campestris
Phagnalon rupestre
Phlomoides ostrowskiana
Phlox paniculata
Piliostigma thonningii
Pimpinella peregrina
Pinguicula vulgaris
Pinus bungeana
Pinus lambertiana
Pinus monticola
Pinus parviflora
Pinus pumila
Pinus strobus
Piper callosum
Piper hostmannianum
Pittocaulon bombycophole
Polyachyrus sphaerocephalus
Pongamiopsis pervilleana
Prioria pinnata
Pseudoconyza viscosa
Pseudotsuga sinensis var. sinensis
Rubus pungens
Salix petiolaris
Salvia barrelieri
Salvia lanigera
Salvia pisidica
Sanguisorba minor
Scutellaria baicalensis
Semialarium mexicanum
Sideritis lanata
Solanum crinitum
Syzygium cumini
Syzygium samarangense
Tamarix gallica
Thelypteris palustris
Thermopsis mollis
Tubocapsicum anomalum
Uncaria longiflora
Ursinia speciosa
Viola hondoensis

Cross-Links

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PubChem 442520
NPASS NPC312391
LOTUS LTS0190343
wikiData Q27108348