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Hirtellins T1
- Family: Plantae - Tamaricaceae
- Kingdom: Plantae
-
Class: Tannin
- Subclass: Ellagitannin Trimer
Canonical Smiles | O=C(c1cc(O)c(c(c1)Oc1c(cc(c(c1O)O)O)C(=O)OC1[C@@H](OC2[C@H]([C@@H]1OC(=O)c1cc(O)c(c(c1)O)O)OC(=O)c1cc(O)c(c(c1c1c(C(=O)OC2)cc(c(c1O)O)O)O)O)OC(=O)c1cc(O)c(c(c1)O)O)O)O[C@@H]1OC2COC(=O)c3cc(O)c(c(c3c3c(C(=O)O[C@H]2[C@@H](C1OC(=O)c1cc(O)c(c(c1Oc1cc(cc(c1O)O)C(=O)O[C@@H]1O[C@@H]2COc4cc(O)c(c(c4c4c(C(=O)OC2C([C@H]1OC(=O)c1cc(O)c(c(c1)O)O)OC(=O)c1cc(O)c(c(c1)O)O)cc(c(c4O)O)O)O)O)O)O)OC(=O)c1cc(O)c(c(c1)O)O)cc(O)c(c3O)O)O)O |
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InChI | InChI=1S/C122H86O77/c123-40-1-26(2-41(124)72(40)143)106(166)191-100-97-63(23-180-60-22-59(142)84(155)92(163)71(60)70-37(117(177)188-97)19-56(139)83(154)91(70)162)185-120(103(100)194-109(169)29-7-46(129)75(146)47(130)8-29)198-111(171)31-11-50(133)77(148)61(13-31)183-96-39(21-58(141)86(157)94(96)165)119(179)196-105-102(193-108(168)28-5-44(127)74(145)45(128)6-28)99-65(25-182-114(174)34-16-53(136)80(151)88(159)67(34)69-36(116(176)190-99)18-55(138)82(153)90(69)161)187-122(105)199-112(172)32-12-51(134)78(149)62(14-32)184-95-38(20-57(140)85(156)93(95)164)118(178)195-104-101(192-107(167)27-3-42(125)73(144)43(126)4-27)98-64(186-121(104)197-110(170)30-9-48(131)76(147)49(132)10-30)24-181-113(173)33-15-52(135)79(150)87(158)66(33)68-35(115(175)189-98)17-54(137)81(152)89(68)160/h1-22,63-65,97-105,120-165H,23-25H2/t63-,64?,65?,97?,98-,99-,100?,101+,102+,103-,104?,105?,120+,121+,122+/m1/s1 |
InChIKey | XSOGTZFKQRCIMY-QPSURAOZSA-N |
Formula | C122H86O77 |
HBA | 77 |
HBD | 43 |
MW | 2783.95 |
Rotatable Bonds | 22 |
TPSA | 1293.47 |
LogP | 6.02 |
Number Rings | 21 |
Number Aromatic Rings | 15 |
Heavy Atom Count | 199 |
Formal Charge | 0 |
Fraction CSP3 | 0.15 |
Exact Mass | 2782.28 |
Number of Lipinski Rule Violations | 4 |
# | Species | Family | Kingdom | NCBI Taxonomy ID |
---|---|---|---|---|
1 | Tamarix tetrandra | Tamaricaceae | Plantae | 1491188 |
Showing of synonyms
Hirtellins T1
No compound-protein relationship available.
No scaffolds available.
No bioactivities available.
Absorption
- Caco-2 (logPapp)
- -
- Human Oral Bioavailability 20%
- -
- Human Intestinal Absorption
- -
- Madin-Darby Canine Kidney
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- Human Oral Bioavailability 50%
- -
- P-Glycoprotein Inhibitor
- -
- P-Glycoprotein Substrate
- -
- Skin Permeability
- -
Distribution
- Blood-Brain Barrier (CNS)
- -
- Blood-Brain Barrier
- -
- Fraction Unbound (Human)
- -
- Plasma Protein Binding
- -
- Steady State Volume of Distribution
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Metabolism
- Breast Cancer Resistance Protein
- -
- CYP 1A2 Inhibitor
- -
- CYP 1A2 Substrate
- -
- CYP 2C19 Inhibitor
- -
- CYP 2C19 Substrate
- -
- CYP 2C9 Inhibitor
- -
- CYP 2C9 Substrate
- -
- CYP 2D6 Inhibitor
- -
- CYP 2D6 Substrate
- -
- CYP 3A4 Inhibitor
- -
- CYP 3A4 Substrate
- -
- OATP1B1
- -
- OATP1B3
- -
Excretion
- Clearance
- -
- Organic Cation Transporter 2
- -
- Half-Life of Drug
- -
Toxicity
- AMES Mutagenesis
- -
- Avian
- -
- Bee
- -
- Bioconcentration Factor
- -
- Biodegradation
- -
- Carcinogenesis
- -
- Crustacean
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- Liver Injury I (DILI)
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- Eye Corrosion
- -
- Eye Irritation
- -
- Maximum Tolerated Dose
- -
- Liver Injury II
- -
- hERG Blockers
- -
- Daphnia Maga
- -
- Micronucleos
- -
- NR-AhR
- -
- NR-AR
- -
- NR-AR-LBD
- -
- NR-Aromatase
- -
- NR-ER
- -
- NR-ER-LBD
- -
- NR-GR
- -
- NR-PPAR-gamma
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- NR-TR
- -
- T. Pyriformis
- -
- Rat (Acute)
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- Rat (Chronic Oral)
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- Fathead Minnow
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- Respiratory Disease
- -
- Skin Sensitisation
- -
- SR-ARE
- -
- SR-ATAD5
- -
- SR-HSE
- -
- SR-MMP
- -
- SR-p53
- -
General Properties
- Boiling Point
- -
- Hydration Free Energy
- -
- Log(D) at pH=7.4
- -
- Log(P)
- -
- Log S
- -
- Log(Vapor Pressure)
- -
- Melting Point
- -
- pKa Acid
- -
- pKa Basic
- -
No predicted protein targets found for this compound.