(Thr(2),Ile(5))Cyclosporin

Details

Top
Internal ID d0b4a31f-85ae-4a5c-8c5d-a749c19c1f91
Taxonomy Organic acids and derivatives > Peptidomimetics > Peptoid-peptide hybrids > Cyclosporins
IUPAC Name (3S,6S,9S,12R,15S,18S,21S,24S,33S)-21-butan-2-yl-30-[(1R)-1-hydroxyethyl]-33-[(E,1R,2R)-1-hydroxy-2-methylhex-4-enyl]-1,4,7,10,12,15,19,25,28-nonamethyl-6,9,18,24-tetrakis(2-methylpropyl)-3-propan-2-yl-1,4,7,10,13,16,19,22,25,28,31-undecazacyclotritriacontane-2,5,8,11,14,17,20,23,26,29,32-undecone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C63H113N11O13/c1-25-27-28-40(14)53(77)52-57(81)67-50(43(17)75)61(85)68(18)33-48(76)69(19)44(29-34(3)4)56(80)66-49(39(13)26-2)62(86)70(20)45(30-35(5)6)55(79)64-41(15)54(78)65-42(16)58(82)71(21)46(31-36(7)8)59(83)72(22)47(32-37(9)10)60(84)73(23)51(38(11)12)63(87)74(52)24/h25,27,34-47,49-53,75,77H,26,28-33H2,1-24H3,(H,64,79)(H,65,78)(H,66,80)(H,67,81)/b27-25+/t39?,40-,41+,42-,43-,44+,45+,46+,47+,49+,50?,51+,52+,53-/m1/s1
InChI Key IZUOWPDPGMBNCB-XSAWRUQVSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C63H113N11O13
Molecular Weight 1232.60 g/mol
Exact Mass 1231.85193270 g/mol
Topological Polar Surface Area (TPSA) 299.00 Ų
XlogP 7.30
Atomic LogP (AlogP) 2.63
H-Bond Acceptor 13
H-Bond Donor 6
Rotatable Bonds 16

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (Thr(2),Ile(5))Cyclosporin

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.4710 47.10%
Caco-2 - 0.8590 85.90%
Blood Brain Barrier - 0.9250 92.50%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.6346 63.46%
OATP2B1 inhibitior - 0.8572 85.72%
OATP1B1 inhibitior - 0.5172 51.72%
OATP1B3 inhibitior - 0.4846 48.46%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.9534 95.34%
P-glycoprotein inhibitior + 0.7402 74.02%
P-glycoprotein substrate + 0.7831 78.31%
CYP3A4 substrate + 0.7465 74.65%
CYP2C9 substrate - 0.8284 82.84%
CYP2D6 substrate - 0.8475 84.75%
CYP3A4 inhibition - 0.6706 67.06%
CYP2C9 inhibition - 0.9212 92.12%
CYP2C19 inhibition - 0.8867 88.67%
CYP2D6 inhibition - 0.9262 92.62%
CYP1A2 inhibition - 0.9069 90.69%
CYP2C8 inhibition + 0.5673 56.73%
CYP inhibitory promiscuity - 0.9954 99.54%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Non-required 0.5993 59.93%
Eye corrosion - 0.9847 98.47%
Eye irritation - 0.8982 89.82%
Skin irritation - 0.7594 75.94%
Skin corrosion - 0.9136 91.36%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3774 37.74%
Micronuclear + 0.7300 73.00%
Hepatotoxicity + 0.8125 81.25%
skin sensitisation - 0.8757 87.57%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.6313 63.13%
Acute Oral Toxicity (c) III 0.7604 76.04%
Estrogen receptor binding + 0.7708 77.08%
Androgen receptor binding + 0.7313 73.13%
Thyroid receptor binding + 0.6496 64.96%
Glucocorticoid receptor binding + 0.7194 71.94%
Aromatase binding + 0.5821 58.21%
PPAR gamma + 0.7957 79.57%
Honey bee toxicity - 0.7754 77.54%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.7400 74.00%
Fish aquatic toxicity - 0.5253 52.53%

Targets

Top

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
CHEMBL2581 P07339 Cathepsin D 99.13% 98.95%
CHEMBL1949 P62937 Cyclophilin A 98.92% 98.57%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.18% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.21% 97.25%
CHEMBL4072 P07858 Cathepsin B 94.37% 93.67%
CHEMBL1937 Q92769 Histone deacetylase 2 93.34% 94.75%
CHEMBL5103 Q969S8 Histone deacetylase 10 91.84% 90.08%
CHEMBL321 P14780 Matrix metalloproteinase 9 91.51% 92.12%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.62% 95.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 89.28% 90.71%
CHEMBL333 P08253 Matrix metalloproteinase-2 88.85% 96.31%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.66% 97.09%
CHEMBL4208 P20618 Proteasome component C5 87.58% 90.00%
CHEMBL255 P29275 Adenosine A2b receptor 87.38% 98.59%
CHEMBL3267 P48736 PI3-kinase p110-gamma subunit 87.35% 95.71%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.81% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.44% 99.23%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 84.77% 90.93%
CHEMBL4588 P22894 Matrix metalloproteinase 8 84.28% 94.66%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.16% 89.00%
CHEMBL332 P03956 Matrix metalloproteinase-1 82.43% 94.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.86% 99.17%
CHEMBL2730 P21980 Protein-glutamine gamma-glutamyltransferase 81.43% 92.38%
CHEMBL3492 P49721 Proteasome Macropain subunit 81.29% 90.24%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.13% 93.56%

Plants that contains it

Top
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.
There are no matching plants.

Cross-Links

Top
PubChem 139588480
LOTUS LTS0028117
wikiData Q105123489