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Hirtellin T1
- Family: Plantae - Tamaricaceae
- Kingdom: Plantae
- Class: Tannin
Canonical Smiles | O=C(Oc1cc(O)c(c(c1Oc1cc(cc(c1O)O)C(=O)O[C@@H]1O[C@@H]2COC(=O)c3cc(O)c(c(c3c3c(C(=O)O[C@H]2[C@@H]([C@H]1OC(=O)c1cc(O)c(c(c1)O)O)O)cc(O)c(c3O)O)O)O)O)O)O[C@@H]1[C@H](O[C@H]2[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)Oc1cc(O)c(c(c1C(=O)O[C@@H]1[C@H](O[C@H]2[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)O |
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InChI | InChI=1S/C116H82O75/c117-36-1-24(2-37(118)68(36)135)100(158)184-95-90(157)92-58(21-172-106(164)30-13-46(127)74(141)82(149)61(30)64-33(109(167)181-92)16-49(130)77(144)85(64)152)177-113(95)189-104(162)29-10-45(126)73(140)56(12-29)176-91-57(20-53(134)81(148)89(91)156)180-116(171)188-99-97(186-102(160)26-5-40(121)70(137)41(122)6-26)94-60(23-174-108(166)32-15-48(129)76(143)84(151)63(32)66-35(111(169)183-94)18-51(132)79(146)87(66)154)179-115(99)191-105(163)28-9-44(125)72(139)55(11-28)175-54-19-52(133)80(147)88(155)67(54)112(170)187-98-96(185-101(159)25-3-38(119)69(136)39(120)4-25)93-59(178-114(98)190-103(161)27-7-42(123)71(138)43(124)8-27)22-173-107(165)31-14-47(128)75(142)83(150)62(31)65-34(110(168)182-93)17-50(131)78(145)86(65)153/h1-20,58-60,90,92-99,113-115,117-157H,21-23H2/t58-,59-,60-,90+,92-,93+,94+,95-,96-,97+,98+,99+,113+,114-,115-/m1/s1 |
InChIKey | FQVUARZAIIKZEI-JXLJMMAHSA-N |
Formula | C116H82O75 |
HBA | 75 |
HBD | 41 |
MW | 2675.86 |
Rotatable Bonds | 20 |
TPSA | 1253.01 |
LogP | 5.18 |
Number Rings | 20 |
Number Aromatic Rings | 14 |
Heavy Atom Count | 191 |
Formal Charge | 0 |
Fraction CSP3 | 0.16 |
Exact Mass | 2674.26 |
Number of Lipinski Rule Violations | 4 |
# | Species | Family | Kingdom | NCBI Taxonomy ID |
---|---|---|---|---|
1 | Tamarix nilotica | Tamaricaceae | Plantae | 189799 |
2 | Tamarix tetrandra | Tamaricaceae | Plantae | 1491188 |
Showing of synonyms
Hirtellin T1
No compound-protein relationship available.
No scaffolds available.
Tumor-selective cytotoxic
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
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- P-Glycoprotein Substrate
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- Skin Permeability
- -
Distribution
- Blood-Brain Barrier (CNS)
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- Blood-Brain Barrier
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- Fraction Unbound (Human)
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- Plasma Protein Binding
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- Steady State Volume of Distribution
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Metabolism
- Breast Cancer Resistance Protein
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- CYP 1A2 Inhibitor
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- CYP 1A2 Substrate
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- CYP 2C19 Inhibitor
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- CYP 2C19 Substrate
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- CYP 2C9 Inhibitor
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- CYP 2C9 Substrate
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- CYP 2D6 Inhibitor
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- CYP 2D6 Substrate
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- CYP 3A4 Inhibitor
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- CYP 3A4 Substrate
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- OATP1B1
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- OATP1B3
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Excretion
- Clearance
- -
- Organic Cation Transporter 2
- -
- Half-Life of Drug
- -
Toxicity
- AMES Mutagenesis
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- Avian
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- Bee
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- Bioconcentration Factor
- -
- Biodegradation
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- Carcinogenesis
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- Crustacean
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- Liver Injury I (DILI)
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- Eye Corrosion
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- Eye Irritation
- -
- Maximum Tolerated Dose
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- Liver Injury II
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- hERG Blockers
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- Daphnia Maga
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- Micronucleos
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- NR-AhR
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- NR-AR
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- NR-AR-LBD
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- NR-Aromatase
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- NR-ER
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- NR-ER-LBD
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- NR-GR
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- NR-PPAR-gamma
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- NR-TR
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- T. Pyriformis
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- Rat (Acute)
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- Rat (Chronic Oral)
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- Fathead Minnow
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- Respiratory Disease
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- Skin Sensitisation
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- SR-ARE
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- SR-ATAD5
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- SR-HSE
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- SR-MMP
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- SR-p53
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General Properties
- Boiling Point
- -
- Hydration Free Energy
- -
- Log(D) at pH=7.4
- -
- Log(P)
- -
- Log S
- -
- Log(Vapor Pressure)
- -
- Melting Point
- -
- pKa Acid
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- pKa Basic
- -
No predicted protein targets found for this compound.