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Aristolochia mollissima

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID64400aa17f647268410236
Scientific name Aristolochia mollissima
Authority Hance
First published in J. Bot. 17: 300 (1879)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Chinese 毛香
Chinese 猫耳朵草
Chinese 寻骨风
Chinese 寻骨风（绵毛马兜铃）
Chinese 绵毛马兜铃
Chinese 毛风草
Chinese 烟袋锅
Chinese 猴耳草
Chinese 白毛藤
Chinese 穿地筋
Chinese 黄才香
Chinese 尋骨風

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000548087
Tropicos 2500550
KEW urn:lsid:ipni.org:names:93147-1
The Plant List kew-2651673
Open Tree Of Life 656355
NCBI Taxonomy 158558
IPNI 93147-1
GBIF 3588500
EOL 2872746
USDA GRIN 4101

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Phytochemical and pharmacological studies on Solanum lyratum: a review Zhao Y, Gao WK, Wang XD, Zhang LH, Yu HY, Wu HH Nat Prod Bioprospect 09-Nov-2022
PMCID:PMC9643311
doi:10.1007/s13659-022-00361-0
PMID:36348127
Qingfei Jiedu decoction inhibits PD-L1 expression in lung adenocarcinoma based on network pharmacology analysis, molecular docking and experimental verification Pan J, Yang H, Zhu L, Lou Y, Jin B Front Pharmacol 22-Aug-2022
PMCID:PMC9454399
doi:10.3389/fphar.2022.897966
PMID:36091822
Asari Radix et Rhizoma consumption lacks relevance for hepatocellular carcinoma in patients: A retrospective cohort study Fang ZE, Guo Y, Wang Z, He T, Wang J, Bai Z, Xiao X Chin Herb Med 26-Mar-2022
PMCID:PMC9476760
doi:10.1016/j.chmed.2022.01.004
PMID:36117998
Quantitative Determination and Toxicity Evaluation of Aristolochic Acid Analogues in Asarum heterotropoides F. Schmidt (Xixin) and Traditional Chinese Patent Medicines Liu S, Xian Z, Zhao Y, Wang L, Tian J, Pan C, Han J, Zhang Y, Li C, Yi Y, Liu C, Wang D, Meng J, Qin S, Wang F, Liang A Front Pharmacol 26-Nov-2021
PMCID:PMC8662950
doi:10.3389/fphar.2021.761593
PMID:34899315
Natural Bioactive Cinnamoyltyramine Alkylamides and Co-Metabolites Evidente A, Masi M Biomolecules 25-Nov-2021
PMCID:PMC8698393
doi:10.3390/biom11121765
PMID:34944409
Verification of Thai ethnobotanical medicine “Kamlang Suea Khrong” driven by multiplex PCR and powerful TLC techniques Yanaso S, Phrutivorapongkul A, Hongwiset D, Piyamongkol S, Intharuksa A PLoS One 17-Sep-2021
PMCID:PMC8448358
doi:10.1371/journal.pone.0257243
PMID:34534243
Computational Analysis of Naturally Occurring Aristolochic Acid Analogues and Their Biological Sources Xu T, Chen W, Zhou J, Dai J, Li Y, Zhao Y Biomolecules 11-Sep-2021
PMCID:PMC8471445
doi:10.3390/biom11091344
PMID:34572557
Nephrotoxicity of Herbal Medicine and Its Prevention Xu X, Zhu R, Ying J, Zhao M, Wu X, Cao G, Wang K Front Pharmacol 15-Oct-2020
PMCID:PMC7593559
doi:10.3389/fphar.2020.569551
PMID:33178019
A Review of the Effects of Natural Compounds, Medicinal Plants, and Mushrooms on the Gut Microbiota in Colitis and Cancer Cheung MK, Yue GG, Chiu PW, Lau CB Front Pharmacol 15-May-2020
PMCID:PMC7243258
doi:10.3389/fphar.2020.00744
PMID:32499711
Recent developments in detoxication techniques for aristolochic acid-containing traditional Chinese medicines Fan Y, Li Z, Xi J RSC Adv 08-Jan-2020
PMCID:PMC9048270
doi:10.1039/c9ra08327h
PMID:35494720
The complete chloroplast genome sequence of Aristolochia manshuriensis Kom. (Aristolochiaceae) Kim K, Lim CE Mitochondrial DNA B Resour 11-Oct-2019
PMCID:PMC7707360
doi:10.1080/23802359.2019.1675484
PMID:33366065
Systematic Overview of Aristolochic Acids: Nephrotoxicity, Carcinogenicity, and Underlying Mechanisms Han J, Xian Z, Zhang Y, Liu J, Liang A Front Pharmacol 11-Jun-2019
PMCID:PMC6580798
doi:10.3389/fphar.2019.00648
PMID:31244661
Regulation of Shaoyao Ruangan Mixture on Intestinal Flora in Mice With Primary Liver Cancer Zhen H, Qian X, Fu X, Chen Z, Zhang A, Shi L Integr Cancer Ther 22-Apr-2019
PMCID:PMC6477757
doi:10.1177/1534735419843178
PMID:31006277
Complete Chloroplast Genomes and Comparative Analysis of Sequences Evolution among Seven Aristolochia (Aristolochiaceae) Medicinal Species Li X, Zuo Y, Zhu X, Liao S, Ma J Int J Mol Sci 28-Feb-2019
PMCID:PMC6429227
doi:10.3390/ijms20051045
PMID:30823362
Sequence-Specific Detection of Aristolochia DNA – A Simple Test for Contamination of Herbal Products Sgamma T, Masiero E, Mali P, Mahat M, Slater A Front Plant Sci 11-Dec-2018
PMCID:PMC6297175
doi:10.3389/fpls.2018.01828
PMID:30619401

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Aporphines
Aristoliukine B 135426385 Click to see COC1=C2C3=CC(=O)C=CC3=CC4=C2C(=CC1=O)C(=C(N4)O)O 309.27 unknown https://doi.org/10.1021/NP0002886
Cepharadione A 94577 Click to see CN1C2=CC3=CC=CC=C3C4=C2C(=CC5=C4OCO5)C(=O)C1=O 305.30 unknown https://doi.org/10.1021/NP0002886
> Alkaloids and derivatives / Aporphines / 4,5-dioxoaporphines
4,15-dihydroxy-16-methoxy-10-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1,3,5,7,9(17),13,15-heptaene-11,12-dione 10709985 Click to see COC1=C(C=C2C3=C(C=C4C=CC(=CC4=C31)O)NC(=O)C2=O)O 309.27 unknown https://doi.org/10.1021/NP0002886
Noraristolodione 10108434 Click to see COC1=C(C=C2C3=C1C4=CC=CC=C4C=C3NC(=O)C2=O)O 293.27 unknown https://doi.org/10.1021/NP0002886
> Alkaloids and derivatives / Aristolactams
10-[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]-3,5-dioxa-10-azapentacyclo[9.7.1.02,6.08,19.013,18]nonadeca-1(19),2(6),7,11,13,15,17-heptaen-9-one 162881428 Click to see C1OC2=C(O1)C3=C4C(=C2)C(=O)N(C4=CC5=CC=CC=C53)C6C(C(C(C(O6)CO)O)O)O 425.40 unknown https://doi.org/10.1248/CPB.47.887
14-hydroxy-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-3,5-dioxa-10-azapentacyclo[9.7.1.02,6.08,19.013,18]nonadeca-1(18),2(6),7,11(19),12,14,16-heptaen-9-one 162999109 Click to see C1OC2=C(O1)C3=C4C=CC=C(C4=CC5=C3C(=C2)C(=O)N5C6C(C(C(C(O6)CO)O)O)O)O 441.40 unknown https://doi.org/10.1021/NP0002886
14-Hydroxy-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-3,5-dioxa-10-azapentacyclo[9.7.1.02,6.08,19.013,18]nonadeca-1(18),2(6),7,11(19),12,14,16-heptaen-9-one 162999108 Click to see C1OC2=C(O1)C3=C4C=CC=C(C4=CC5=C3C(=C2)C(=O)N5C6C(C(C(C(O6)CO)O)O)O)O 441.40 unknown https://doi.org/10.1021/NP0002886
14-methoxy-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-3,5-dioxa-10-azapentacyclo[9.7.1.02,6.08,19.013,18]nonadeca-1(18),2(6),7,11(19),12,14,16-heptaen-9-one 10411690 Click to see COC1=CC=CC2=C3C4=C(C=C21)N(C(=O)C4=CC5=C3OCO5)C6C(C(C(C(O6)CO)O)O)O 455.40 unknown https://doi.org/10.1021/NP0002886
4,14-Dihydroxy-13-(hydroxymethyl)-15-methoxy-10-azatetracyclo[7.6.1.02,7.012,16]hexadeca-1,3,5,7,9(16),12,14-heptaen-11-one 10757387 Click to see COC1=C(C(=C2C3=C(C=C4C=CC(=CC4=C31)O)NC2=O)CO)O 311.29 unknown https://doi.org/10.1021/NP0002886
Aristolactam AII 148657 Click to see COC1=C(C=C2C3=C1C4=CC=CC=C4C=C3NC2=O)O 265.26 unknown https://doi.org/10.1021/NP0002886
Aristolactam AIIIa 10356352 Click to see COC1=C(C=C2C3=C(C=C4C=CC(=CC4=C31)O)NC2=O)O 281.26 unknown https://doi.org/10.1021/NP0002886
> Benzenoids / Phenanthrenes and derivatives / Aristolochic acids and derivatives
[(2S)-1-[(5R,6S)-5-ethenyl-5-methyl-6-(3-oxoprop-1-en-2-yl)cyclohexen-1-yl]propan-2-yl] 8-methoxy-6-nitronaphtho[2,1-g][1,3]benzodioxole-5-carboxylate 10602894 Click to see CC(CC1=CCCC(C1C(=C)C=O)(C)C=C)OC(=O)C2=CC3=C(C4=C5C=CC=C(C5=CC(=C24)[N+](=O)[O-])OC)OCO3 557.60 unknown https://doi.org/10.1021/NP0002886
Aristolochic acid 2236 Click to see COC1=CC=CC2=C3C(=C(C=C21)[N+](=O)[O-])C(=CC4=C3OCO4)C(=O)O 341.27 unknown https://doi.org/10.1021/NP0002886
https://doi.org/10.1248/CPB.47.887
Aristolochic acid d 161218 Click to see COC1=CC(=CC2=C3C(=C(C=C12)[N+](=O)[O-])C(=CC4=C3OCO4)C(=O)O)O 357.30 unknown https://doi.org/10.1021/NP0002886
Aristolochic acid I methyl ester 96709 Click to see COC1=CC=CC2=C3C(=C(C=C21)[N+](=O)[O-])C(=CC4=C3OCO4)C(=O)OC 355.30 unknown https://doi.org/10.1248/CPB.47.887
Aristolochic acid II 108168 Click to see C1OC2=C(O1)C3=C(C(=C2)C(=O)O)C(=CC4=CC=CC=C43)[N+](=O)[O-] 311.24 unknown https://doi.org/10.1021/NP0002886
Aristoloterpenate III 163184387 Click to see CC1=CCCC(=CC(CC(=CCC1)C)OC(=O)C2=CC3=C(C4=C5C=CC=C(C5=CC(=C24)[N+](=O)[O-])OC)OCO3)C=O 557.60 unknown https://doi.org/10.1021/NP0002886
Aristophyllide A 10840539 Click to see CC(CC1=CCCC(C1C(=C)C=O)(C)C=C)OC(=O)C2=CC3=C(C4=C5C=CC=C(C5=CC(=C24)[N+](=O)[O-])OC)OCO3 557.60 unknown https://doi.org/10.1021/NP0002886
> Benzenoids / Phenanthrenes and derivatives / Phenanthrols
12,14-Dimethoxy-3,5-dioxa-10-azapentacyclo[9.7.1.02,6.08,19.013,18]nonadeca-1(19),2(6),7,11,13(18),14,16-heptaen-9-one 14804089 Click to see COC1=CC=CC2=C1C(=C3C4=C2C5=C(C=C4C(=O)N3)OCO5)OC 323.30 unknown https://doi.org/10.1021/NP0002886
> Benzenoids / Phenols / Methoxyphenols
(4S)-8-(4-hydroxy-3-methoxyphenyl)-6-oxooctane-4-sulfonic acid 162849811 Click to see CCCC(CC(=O)CCC1=CC(=C(C=C1)O)OC)S(=O)(=O)O 330.40 unknown https://doi.org/10.1002/JCCS.200100117
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol 64685 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1021/NP0002886
trans-Borneol 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1021/NP0002886
https://doi.org/10.1248/CPB.47.887
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1021/NP0002886
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1021/NP0002886
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
Isobicyclogermacral 13818876 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C=O 218.33 unknown https://doi.org/10.1021/NP0002886
Isobicyclogermacrenal 129685966 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C=O 218.33 unknown https://doi.org/10.1021/NP0002886
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(1S,2E,6Z,10R,11S)-11-(hydroxymethyl)-7,11-dimethylbicyclo[8.1.0]undeca-2,6-diene-3-carbaldehyde 101018775 Click to see CC1=CCCC(=CC2C(C2(C)CO)CC1)C=O 234.33 unknown https://doi.org/10.1021/NP0002886
Madolin K 71720024 Click to see CC1=CCCC(=CC2C(C2(C)CO)CC1)C=O 234.33 unknown https://doi.org/10.1021/NP0002886
Madolin T 71720025 Click to see CC1=CCCC(=CC2C(C2(C)COC(=O)C)CC1)C=O 276.40 unknown https://doi.org/10.1021/NP0002886
https://doi.org/10.1248/CPB.47.887
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1S,4S,8R,9R)-4-hydroxy-5-methyl-8-prop-1-en-2-yl-10-oxabicyclo[7.2.1]dodec-5-en-11-one 71717614 Click to see CC1=CCC(C2CC(CCC1O)C(=O)O2)C(=C)C 250.33 unknown https://doi.org/10.1021/NP0002886
https://doi.org/10.1248/CPB.47.887
(4Z,8R,9R)-5-methyl-8-prop-1-en-2-yl-10-oxabicyclo[7.2.1]dodeca-1(12),4-dien-11-one 101281337 Click to see CC1=CCCC2=CC(C(CC1)C(=C)C)OC2=O 232.32 unknown https://doi.org/10.1021/NP0002886
https://doi.org/10.1248/CPB.47.887
(5E,8R)-4-hydroxy-5-methyl-8-prop-1-en-2-yl-10-oxabicyclo[7.2.1]dodec-5-en-11-one 163185505 Click to see CC1=CCC(C2CC(CCC1O)C(=O)O2)C(=C)C 250.33 unknown https://doi.org/10.1021/NP0002886
Madolin U 71717615 Click to see CC(=C)C1CCC(=C)C(CCC2=CC1OC2=O)O 248.32 unknown https://doi.org/10.1021/NP0002886
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1021/NP0002886
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1021/NP0002886
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown https://doi.org/10.1021/NP0002886
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1021/NP0002886
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
[(1R,2R,5E,9Z,11S)-9-formyl-1,5-dimethyl-2-bicyclo[9.1.0]dodeca-5,9-dienyl] acetate 15385783 Click to see CC1=CCCC(=CC2CC2(C(CC1)OC(=O)C)C)C=O 276.40 unknown https://doi.org/10.1021/NP0002886
Madolin H 91810640 Click to see CC1=CCCC(=CC2CC2(C(CC1)OC(=O)C)C)C=O 276.40 unknown https://doi.org/10.1021/NP0002886
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
(1R,2E,6Z,10S,11S)-10-hydroxy-7,11-dimethylbicyclo[9.1.0]dodeca-2,6-diene-3-carbaldehyde 101093875 Click to see CC1=CCCC(=CC2CC2(C(CC1)O)C)C=O 234.33 unknown https://doi.org/10.1021/NP0002886
(1R,2Z,6E,10S,11S)-10-hydroxy-7,11-dimethylbicyclo[9.1.0]dodeca-2,6-diene-3-carbaldehyde 162847353 Click to see CC1=CCCC(=CC2CC2(C(CC1)O)C)C=O 234.33 unknown https://doi.org/10.1021/NP0002886
> Organic oxygen compounds / Organooxygen compounds / Ethers / Dialkyl ethers
(1Z,3R,5Z,9E)-3-methoxy-5,9-dimethylcyclododeca-1,5,9-triene-1-carbaldehyde 15870762 Click to see CC1=CCCC(=CC(CC(=CCC1)C)OC)C=O 248.36 unknown https://doi.org/10.1021/NP0002886
Madolin M 91864496 Click to see CC1=CCCC(=CC(CC(=CCC1)C)OC)C=O 248.36 unknown https://doi.org/10.1021/NP0002886
> Organoheterocyclic compounds / Azoles / Imidazoles
Allantoin 204 Click to see C1(C(=O)NC(=O)N1)NC(=O)N 158.12 unknown https://doi.org/10.1248/CPB.47.887
https://doi.org/10.1021/NP0002886
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
(4Z,8Z,11S)-5,9-dimethyl-12-oxabicyclo[9.2.1]tetradeca-1(14),4,8-trien-13-one 101032442 Click to see CC1=CCCC2=CC(CC(=CCC1)C)OC2=O 232.32 unknown https://doi.org/10.1021/NP0002886
Manshurolide 14527198 Click to see CC1=CCCC2=CC(CC(=CCC1)C)OC2=O 232.32 unknown https://doi.org/10.1021/NP0002886
Versicolactone A 5315198 Click to see CC1=CCCC2=CC(CC(=CCC1)C)OC2=O 232.32 unknown https://doi.org/10.1016/S0040-4039(01)90885-8
> Organoheterocyclic compounds / Epoxides
Madolin A 10561685 Click to see CC1(C2C1C=C(CCC3C(O3)(CC2)C)C=O)C 234.33 unknown https://doi.org/10.1021/NP0002886
https://doi.org/10.1248/CPB.47.887
Madolin B 10562641 Click to see CC1(C2C1C=C(CCC3C(O3)(CC2)C)C(=O)O)C 250.33 unknown https://doi.org/10.1021/NP0002886
> Organoheterocyclic compounds / Tetrapyrroles and derivatives
methyl (3R,21S,22S)-16-ethenyl-11-ethyl-4-hydroxy-12,17,21,26-tetramethyl-22-[3-oxo-3-[(E,7S,11S)-3,7,11,15-tetramethylhexadec-2-enoxy]propyl]-7,23,24,25-tetrazahexacyclo[18.2.1.15,8.110,13.115,18.02,6]hexacosa-1,4,6,8(26),9,11,13(25),14,16,18(24),19-undecaene-3-carboxylate 136706892 Click to see CCC1=C(C2=NC1=CC3=C(C4=C(C(C(=C5C(C(C(=CC6=NC(=C2)C(=C6C)C=C)N5)C)CCC(=O)OCC=C(C)CCCC(C)CCCC(C)CCCC(C)C)C4=N3)C(=O)OC)O)C)C 871.20 unknown https://doi.org/10.1248/CPB.47.887
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
cis-N-p-coumaroyltyramine 13939145 Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC=C(C=C2)O)O 283.32 unknown https://doi.org/10.1021/NP0002886

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