NCBI Taxonomy: 1589828

Opopanax clade (ncbi_taxid: 1589828)

found 83 associated metabolites at clade taxonomy rank level.

Ancestor: apioid superclade

Child Taxonomies: Opopanax, Smyrniopsis, Magydaris, Stefanoffia, Crenosciadium, Petroedmondia

Marmesin

(2S)-2-(2-hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-7-one

C14H14O4 (246.0892044)


Marmesin is a member of psoralens and a tertiary alcohol. 2-(2-Hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-7-one is a natural product found in Zanthoxylum beecheyanum, Zanthoxylum arnottianum, and other organisms with data available. Nodakenetin is found in wild celery. Nodakenetin is a constituent of Angelica species Constituent of Angelica subspecies Nodakenetin is found in wild celery. (+)-marmesin is a marmesin. It is an enantiomer of a nodakenetin. Marmesin is a natural product found in Coronilla scorpioides, Clausena dunniana, and other organisms with data available. S-(+)-Marmesin is a natural coumarin, exhibiting COX-2/5-LOX dual inhibitory activity. (+)-Marmesin. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=13849-08-6 (retrieved 2024-09-04) (CAS RN: 13849-08-6). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

   

Imperatorin

InChI=1/C16H14O4/c1-10(2)5-7-19-16-14-12(6-8-18-14)9-11-3-4-13(17)20-15(11)16/h3-6,8-9H,7H2,1-2H

C16H14O4 (270.0892044)


Imperatorin is a member of the class of psoralens that is psoralen substituted by a prenyloxy group at position 8. Isolated from Angelica dahurica and Angelica koreana, it acts as a acetylcholinesterase inhibitor. It has a role as an EC 3.1.1.7 (acetylcholinesterase) inhibitor and a metabolite. Imperatorin is a natural product found in Allium wallichii, Ammi visnaga, and other organisms with data available. Imperatorin is found in anise. Imperatorin is present in Aegle marmelos (bael fruit) and seeds of Pastinaca sativa (parsnip).Imperatorin is a furocoumarin and a phytochemical that has been isolated from Urena lobata L. (Malvaceae). It is biosynthesized from umbelliferone, a coumarin derivative.Imperatorin has been shown to exhibit anti-hypertrophic and anti-convulsant functions (A7784, A7785).Imperatorin belongs to the family of Furanocoumarins. These are polycyclic aromatic compounds containing a furan ring fused to a coumarin moeity. See also: Angelica Dahurica Root (part of); Aegle marmelos fruit (part of); Ammi majus seed (part of) ... View More ... Imperatorin is found in anise. Imperatorin is present in Aegle marmelos (bael fruit) and seeds of Pastinaca sativa (parsnip).Imperatorin is a furocoumarin and a phytochemical that has been isolated from Urena lobata L. (Malvaceae). It is biosynthesized from umbelliferone, a coumarin derivative A member of the class of psoralens that is psoralen substituted by a prenyloxy group at position 8. Isolated from Angelica dahurica and Angelica koreana, it acts as a acetylcholinesterase inhibitor. D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents > D011564 - Furocoumarins Present in Aegle marmelos (bael fruit) and seeds of Pastinaca sativa (parsnip) INTERNAL_ID 2244; CONFIDENCE Reference Standard (Level 1) CONFIDENCE Reference Standard (Level 1); INTERNAL_ID 2244 Imperatorin is an effective of NO synthesis inhibitor (IC50=9.2 μmol), which also is a BChE inhibitor (IC50=31.4 μmol). Imperatorin is a weak agonist of TRPV1 with EC50 of 12.6±3.2 μM. Imperatorin is an effective of NO synthesis inhibitor (IC50=9.2 μmol), which also is a BChE inhibitor (IC50=31.4 μmol). Imperatorin is a weak agonist of TRPV1 with EC50 of 12.6±3.2 μM.

   

Isopimpinellin

InChI=1/C13H10O5/c1-15-10-7-3-4-9(14)18-12(7)13(16-2)11-8(10)5-6-17-11/h3-6H,1-2H3

C13H10O5 (246.052821)


Isopimpinellin is a member of psoralens. Isopimpinellin is a natural product found in Zanthoxylum mayu, Zanthoxylum ovalifolium, and other organisms with data available. Isopimpinellin is found in angelica. Isopimpinellin is present in the seeds of Pastinaca sativa (parsnip) Isopimpinellin belongs to the family of Furanocoumarins. These are polycyclic aromatic compounds containing a furan ring fused to a coumarin moeity. See also: Angelica keiskei top (part of). Present in the seeds of Pastinaca sativa (parsnip). Isopimpinellin is found in many foods, some of which are carrot, anise, celery stalks, and fennel. Isopimpinellin is found in angelica. Isopimpinellin is present in the seeds of Pastinaca sativa (parsnip D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents > D011564 - Furocoumarins Isopimpinellin, an orally active compound isolated from Glomerella cingulata. Isopimpinellin blocks DNA adduct formation and skin tumor initiation by 7,12-dimethylbenz[a]anthracene. Isopimpinellin possesses anti-leishmania effect[1]. Isopimpinellin, an orally active compound isolated from Glomerella cingulata. Isopimpinellin blocks DNA adduct formation and skin tumor initiation by 7,12-dimethylbenz[a]anthracene. Isopimpinellin possesses anti-leishmania effect[1].

   

Bergapten

4-methoxyfuro[3,2-g]chromen-7-one

C12H8O4 (216.0422568)


Bergapten, also known as O-methylbergaptol or heraclin, belongs to the class of organic compounds known as 5-methoxypsoralens. These are psoralens containing a methoxy group attached at the C5 position of the psoralen group. Bergapten is found, on average, in the highest concentration within a few different foods, such as anises, figs, and parsnips and in a lower concentration in carrots, fennels, and celery stalks. Bergapten has also been detected, but not quantified, in several different foods, such as coconuts, pepper (c. frutescens), corianders, sesbania flowers, and cardamoms. This could make bergapten a potential biomarker for the consumption of these foods. It is also found in rose hip, sweet marjoram, greenthread tea, and tartary buckwheat. Bergapten is a potentially toxic compound. Bergapten is a major constituent of bergamot oil (Citrus bergamia). Present in celery, especially the outer leaves, and other common grocery vegetables. Implicated in photodermatitis among grocery workers. Bergapten was under investigation in clinical trial NCT00533195 "Comparison of UVA1 Phototherapy Versus Photochemotherapy for Patients With Severe Generalized Atopic Dermatitis". Grayish-white microcrystalline powder or yellow fluffy solid. (NTP, 1992) 5-methoxypsoralen is a 5-methoxyfurocoumarin that is psoralen substituted by a methoxy group at position 5. It has a role as a hepatoprotective agent and a plant metabolite. It is a member of psoralens, a 5-methoxyfurocoumarin and an organic heterotricyclic compound. It is functionally related to a psoralen. Bergapten is under investigation in clinical trial NCT00533195 (Comparison of UVA1 Phototherapy Versus Photochemotherapy for Patients With Severe Generalized Atopic Dermatitis). Bergapten is a natural product found in Ficus auriculata, Ficus virens, and other organisms with data available. A linear furanocoumarin that has phototoxic and anti-inflammatory properties, with effects similar to METHOXSALEN. It is used in PUVA THERAPY for the treatment of PSORIASIS. See also: Parsley (part of); Anise (part of); Angelica archangelica root (part of) ... View More ... Bergapten is a major constituent of bergamot oil (Citrus bergamia). Present in celery, esp. the outer leaves, and other common grocery vegetables. Implicated in photodermatitis among grocery workers. It is also found in rose hip, sweet marjoram, greenthread tea, and tartary buckwheat. D - Dermatologicals > D05 - Antipsoriatics > D05B - Antipsoriatics for systemic use > D05BA - Psoralens for systemic use D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents > D011564 - Furocoumarins D000893 - Anti-Inflammatory Agents D003879 - Dermatologic Agents CONFIDENCE standard compound; INTERNAL_ID 1068; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8020; ORIGINAL_PRECURSOR_SCAN_NO 8017 CONFIDENCE standard compound; INTERNAL_ID 1068; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8002; ORIGINAL_PRECURSOR_SCAN_NO 8000 CONFIDENCE standard compound; INTERNAL_ID 1068; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 7952; ORIGINAL_PRECURSOR_SCAN_NO 7950 CONFIDENCE standard compound; INTERNAL_ID 1068; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 7968; ORIGINAL_PRECURSOR_SCAN_NO 7967 CONFIDENCE standard compound; INTERNAL_ID 1068; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8005; ORIGINAL_PRECURSOR_SCAN_NO 8002 CONFIDENCE standard compound; INTERNAL_ID 1068; DATASET 20200303_ENTACT_RP_MIX503; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8376; ORIGINAL_PRECURSOR_SCAN_NO 8372 [Raw Data] CBA84_Bergapten_pos_20eV.txt [Raw Data] CBA84_Bergapten_pos_10eV.txt [Raw Data] CBA84_Bergapten_pos_30eV.txt [Raw Data] CBA84_Bergapten_pos_40eV.txt [Raw Data] CBA84_Bergapten_pos_50eV.txt Bergapten is a natural anti-inflammatory and anti-tumor agent. Bergapten is inhibitory towards mouse and human CYP isoforms. Bergapten is a natural anti-inflammatory and anti-tumor agent. Bergapten is inhibitory towards mouse and human CYP isoforms.

   

Methoxsalen

Methoxsalen, United States Pharmacopeia (USP) Reference Standard

C12H8O4 (216.0422568)


8-methoxypsoralen is an odorless white to cream-colored crystalline solid. Bitter taste followed by tingling sensation. (NTP, 1992) Methoxsalen is a member of the class of psoralens that is 7H-furo[3,2-g]chromen-7-one in which the 9 position is substituted by a methoxy group. It is a constituent of the fruits of Ammi majus. Like other psoralens, trioxsalen causes photosensitization of the skin. It is administered topically or orally in conjunction with UV-A for phototherapy treatment of vitiligo and severe psoriasis. It has a role as a dermatologic drug, an antineoplastic agent, a photosensitizing agent, a cross-linking reagent and a plant metabolite. It is a member of psoralens and an aromatic ether. It is functionally related to a psoralen. A naturally occurring furocoumarin compound found in several species of plants, including Psoralea corylifolia. It is a photoactive substance that forms DNA adducts in the presence of ultraviolet A irradiation. Methoxsalen is a Photoactivated Radical Generator and Psoralen. The mechanism of action of methoxsalen is as a Photoabsorption. The physiologic effect of methoxsalen is by means of Photosensitizing Activity. Methoxsalen is a natural product found in Ammi visnaga, Zanthoxylum mayu, and other organisms with data available. Methoxsalen is a naturally occurring substance isolated from the seeds of the plant Ammi majus with photoactivating properties. As a member of the family of compounds known as psoralens or furocoumarins, methoxsalens exact mechanism of action is unknown; upon photoactivation, methoxsalen has been observed to bind covalently to and crosslink DNA. (NCI04) Methoxsalen is only found in individuals that have used or taken this drug. It is a naturally occurring furocoumarin compound found in several species of plants, including Psoralea corylifolia. It is a photoactive substance that forms DNA adducts in the presence of ultraviolet A irradiation. After activation Methoxsalen binds preferentially to the guanine and cytosine moieties of DNA, leading to cross-linking of DNA, thus inhibiting DNA synthesis and function. A naturally occurring furocoumarin compound found in several species of plants, including Psoralea corylifolia. It is a photoactive substance that forms DNA ADDUCTS in the presence of ultraviolet A irradiation. See also: Angelica archangelica root (part of); Ammi majus seed (part of); Angelica keiskei top (part of) ... View More ... Methoxsalen, also known as oxsoralen or 8-methoxypsoralen, belongs to the class of organic compounds known as 8-methoxypsoralens. These are psoralens containing a methoxy group attached at the C8 position of the psoralen group. Methoxsalen is a drug which is used for the treatment of psoriasis and vitiligo. Methoxsalen is a bitter tasting compound. Methoxsalen is found, on average, in the highest concentration within a few different foods, such as parsnips, parsley, and celery stalks and in a lower concentration in wild carrots, carrots, and fennels. Methoxsalen has also been detected, but not quantified, in several different foods, such as figs, green vegetables, corianders, dills, and fruits. Methoxsalen is a potentially toxic compound. A member of the class of psoralens that is 7H-furo[3,2-g]chromen-7-one in which the 9 position is substituted by a methoxy group. It is a constituent of the fruits of Ammi majus. Like other psoralens, trioxsalen causes photosensitization of the skin. It is administered topically or orally in conjunction with UV-A for phototherapy treatment of vitiligo and severe psoriasis. Present in celery, especies the outer leaves, and other common grocery vegetables. Implicated in photodermatitis among grocery workers. Isolated from Aegle marmelos (bael) D - Dermatologicals > D05 - Antipsoriatics > D05B - Antipsoriatics for systemic use > D05BA - Psoralens for systemic use D - Dermatologicals > D05 - Antipsoriatics > D05A - Antipsoriatics for topical use > D05AD - Psoralens for topical use D019995 - Laboratory Chemicals > D007202 - Indicators and Reagents > D003432 - Cross-Linking Reagents D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents > D011564 - Furocoumarins C274 - Antineoplastic Agent > C186664 - Cytotoxic Chemotherapeutic Agent > C2842 - DNA Binding Agent C1420 - Photosensitizing Agent D003879 - Dermatologic Agents [Raw Data] CBA87_Xanthotoxin_pos_20eV.txt [Raw Data] CBA87_Xanthotoxin_pos_30eV.txt [Raw Data] CBA87_Xanthotoxin_pos_40eV.txt [Raw Data] CBA87_Xanthotoxin_pos_10eV.txt [Raw Data] CBA87_Xanthotoxin_pos_50eV.txt Methoxsalen (8-Methoxypsoralen) is a furanocoumarin compound used in psoralen, used in studies of psoriasis, eczema, vitiligo and some sun-exposed cutaneous lymphomas, and is a P450 inhibitor. Methoxsalen (8-Methoxypsoralen) is a furanocoumarin compound used in psoralen, used in studies of psoriasis, eczema, vitiligo and some sun-exposed cutaneous lymphomas, and is a P450 inhibitor.

   

Falcarinone

(9E)-heptadeca-1,9-dien-4,6-diyn-3-one

C17H22O (242.1670562)


Isolated from Sium sisarum (skirret). Falcarinone is found in many foods, some of which are parsley, green vegetables, caraway, and coffee and coffee products. Falcarinone is found in caraway. Falcarinone is isolated from Sium sisarum (skirret).

   

Peucedanin

6-Hydroxy-2-isopropyl-3-methoxy-5-benzofuranacrylic acid delta-lactone

C15H14O4 (258.0892044)


Peucedanin, also known as 2-isopropyl-3-methoxy-7h-furo[3,2-g]chromen-7-one or 4-methoxy-5-isopropylfuro(2,3:6,7)coumarin, is a member of the class of compounds known as psoralens. Psoralens are organic compounds containing a psoralen moiety, which consists of a furan fused to a chromenone to for 7H-furo[3,2-g]chromen-7-one. Peucedanin is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Peucedanin can be found in carrot, chervil, and wild carrot, which makes peucedanin a potential biomarker for the consumption of these food products. D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents > D011564 - Furocoumarins

   

Umbelliprenin

7-{[(2E,6Z)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]oxy}-2H-chromen-2-one

C24H30O3 (366.21948299999997)


Isolated from Angelica archangelica (angelica). Umbelliprenin is found in many foods, some of which are coriander, fats and oils, herbs and spices, and green vegetables. Umbelliprenin is found in coriander. Umbelliprenin is isolated from Angelica archangelica (angelica

   

Meranzin hydrate

8-(2,3-dihydroxy-3-methylbutyl)-7-methoxy-2H-chromen-2-one

C15H18O5 (278.1154178)


   

Heraclenin

9-{[(2S)-3,3-dimethyloxiran-2-yl]methoxy}-7H-furo[3,2-g]chromen-7-one

C16H14O5 (286.0841194)


Heraclenin is a member of the class of compounds known as psoralens. Psoralens are organic compounds containing a psoralen moiety, which consists of a furan fused to a chromenone to for 7H-furo[3,2-g]chromen-7-one. Heraclenin is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Heraclenin can be found in carrot, lemon, and wild carrot, which makes heraclenin a potential biomarker for the consumption of these food products.

   

Zosimin

2-[(8S)-2-oxo-2H,8H,9H-furo[2,3-h]chromen-8-yl]propan-2-yl (2Z)-2-methylbut-2-enoate

C19H20O5 (328.13106700000003)


Zosimin is a member of the class of compounds known as angular furanocoumarins. Angular furanocoumarins are furanocoumarins, with a structure characterized by a furan ring angularly fused to a coumarin. Zosimin is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Zosimin can be found in carrot and wild carrot, which makes zosimin a potential biomarker for the consumption of these food products. Columbianadin, a natural coumarin from Heracleum hemsleyanum, is known to have various biological activities including anti-inflammatory and anti-cancer effects. Columbianadin, a natural coumarin from Heracleum hemsleyanum, is known to have various biological activities including anti-inflammatory and anti-cancer effects.

   

Prangenin

7H-Furo(3,2-g)(1)benzopyran-7-one, 9-((3,3-dimethyloxiranyl)methoxy)-, (R)- (9CI)

C16H14O5 (286.0841194)


Oxyimperatorin is a natural product found in Ferula sumbul, Angelica dahurica, and Ferula moschata with data available. Oxyimperatorin ((±)-Heraclenin) is a coumarin isolated from Angelica dahurica. Oxyimperatorin ((±)-Heraclenin) is a coumarin isolated from Angelica dahurica.

   

Smyrindiol

(+)-(2S,3R)-3-Hydroxymarmesin

C14H14O5 (262.0841194)


   

Xanthotoxin

9-methoxy-7H-furo[3,2-g]chromen-7-one

C12H8O4 (216.0422568)


   

Imperatorin

Imperatorin

C16H14O4 (270.0892044)


Imperatorin is an effective of NO synthesis inhibitor (IC50=9.2 μmol), which also is a BChE inhibitor (IC50=31.4 μmol). Imperatorin is a weak agonist of TRPV1 with EC50 of 12.6±3.2 μM. Imperatorin is an effective of NO synthesis inhibitor (IC50=9.2 μmol), which also is a BChE inhibitor (IC50=31.4 μmol). Imperatorin is a weak agonist of TRPV1 with EC50 of 12.6±3.2 μM.

   

Bergapten

Bergapten

C12H8O4 (216.0422568)


D - Dermatologicals > D05 - Antipsoriatics > D05B - Antipsoriatics for systemic use > D05BA - Psoralens for systemic use D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents > D011564 - Furocoumarins relative retention time with respect to 9-anthracene Carboxylic Acid is 0.998 D000893 - Anti-Inflammatory Agents D003879 - Dermatologic Agents relative retention time with respect to 9-anthracene Carboxylic Acid is 0.995 Acquisition and generation of the data is financially supported by the Max-Planck-Society IPB_RECORD: 2841; CONFIDENCE confident structure Bergapten is a natural anti-inflammatory and anti-tumor agent. Bergapten is inhibitory towards mouse and human CYP isoforms. Bergapten is a natural anti-inflammatory and anti-tumor agent. Bergapten is inhibitory towards mouse and human CYP isoforms.

   

Methoxsalen

8-Methoxypsoralen

C12H8O4 (216.0422568)


D - Dermatologicals > D05 - Antipsoriatics > D05B - Antipsoriatics for systemic use > D05BA - Psoralens for systemic use D - Dermatologicals > D05 - Antipsoriatics > D05A - Antipsoriatics for topical use > D05AD - Psoralens for topical use D019995 - Laboratory Chemicals > D007202 - Indicators and Reagents > D003432 - Cross-Linking Reagents D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents > D011564 - Furocoumarins C274 - Antineoplastic Agent > C186664 - Cytotoxic Chemotherapeutic Agent > C2842 - DNA Binding Agent relative retention time with respect to 9-anthracene Carboxylic Acid is 0.910 C1420 - Photosensitizing Agent D003879 - Dermatologic Agents relative retention time with respect to 9-anthracene Carboxylic Acid is 0.909 Methoxsalen (8-Methoxypsoralen) is a furanocoumarin compound used in psoralen, used in studies of psoriasis, eczema, vitiligo and some sun-exposed cutaneous lymphomas, and is a P450 inhibitor. Methoxsalen (8-Methoxypsoralen) is a furanocoumarin compound used in psoralen, used in studies of psoriasis, eczema, vitiligo and some sun-exposed cutaneous lymphomas, and is a P450 inhibitor.

   

9-(2,3-dihydroxy-3-methylbutoxy)furo[3,2-g]chromen-7-one

NCGC00179981-03!9-(2,3-dihydroxy-3-methylbutoxy)furo[3,2-g]chromen-7-one

C16H16O6 (304.0946836)


   

8-(2,3-dihydroxy-3-methylbutyl)-7-methoxychromen-2-one

NCGC00169439-02!8-(2,3-dihydroxy-3-methylbutyl)-7-methoxychromen-2-one

C15H18O5 (278.1154178)


   

Umbelliprenin

7-{[(2E,6Z)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]oxy}-2H-chromen-2-one

C24H30O3 (366.21948299999997)


   

Isopimpinellin

Isopimpinellin

C13H10O5 (246.052821)


Isopimpinellin, an orally active compound isolated from Glomerella cingulata. Isopimpinellin blocks DNA adduct formation and skin tumor initiation by 7,12-dimethylbenz[a]anthracene. Isopimpinellin possesses anti-leishmania effect[1]. Isopimpinellin, an orally active compound isolated from Glomerella cingulata. Isopimpinellin blocks DNA adduct formation and skin tumor initiation by 7,12-dimethylbenz[a]anthracene. Isopimpinellin possesses anti-leishmania effect[1].

   

8-(2,3-dihydroxy-3-methylbutyl)-7-methoxychromen-2-one

8-(2,3-dihydroxy-3-methylbutyl)-7-methoxychromen-2-one

C15H18O5 (278.1154178)


   

Osthole

Osthole

C15H16O3 (244.1099386)


Annotation level-1

   

Peucedanin

Peucedanin

C15H14O4 (258.0892044)


A member of the class of furanocoumarins that is furo[3,2-g]chromen-7-one, bearing additional isopropyl and methoxy substituents at positions 2 and 3 respectively. D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents > D011564 - Furocoumarins Origin: Plant, Coumarins

   

Heraclenin

Heraclenin

C16H14O5 (286.0841194)


Origin: Plant, Coumarins Heraclenin, a natural furanocoumarin, significantly inhibits T cell receptor-mediated proliferation in human primary T cells in a concentration-dependent manner by targeting nuclear factor of activated T-cells (NFAT)[1]. Heraclenin, a natural furanocoumarin, significantly inhibits T cell receptor-mediated proliferation in human primary T cells in a concentration-dependent manner by targeting nuclear factor of activated T-cells (NFAT)[1].

   

heraclenol

9-(2,3-dihydroxy-3-methylbutoxy)-2H-furo[3,2-g]chromen-2-one

C16H16O6 (304.0946836)


   

Falcarinol

(CIS)-(-)-3-HYDROXY-1,9-HEPTADECADIEN-4,6-DIYNE

C17H24O (244.18270539999997)


Panaxynol is a long-chain fatty alcohol. It has a role as a metabolite. Falcarinol is a natural product found in Chaerophyllum aureum, Cussonia arborea, and other organisms with data available. A natural product found in Panax ginseng and Angelica japonica.

   

FA 17:7;O

(7E,9E,15E)-heptadeca-7,9,15-trien-11,13-diyn-4-one

C17H20O (240.151407)


   

Falcarinone

(Z)-heptadeca-1,9Z-dien-4,6-diyn-3-one

C17H22O (242.1670562)


   

Marmesin

7H-Furo[3,2g][1]-benzopyran-7-one, (-2,3-dihydro-2-(1-hydroxy-1-hydroxymethylethyl)-, (R)

C14H14O4 (246.0892044)


Nodakenetin is a marmesin with R-configuration. It has a role as a plant metabolite, a rat metabolite and a xenobiotic metabolite. It is an enantiomer of a (+)-marmesin. Nodakenetin is a natural product found in Zanthoxylum beecheyanum, Melicope barbigera, and other organisms with data available. A marmesin with R-configuration. (+)-marmesin is a marmesin. It is an enantiomer of a nodakenetin. Marmesin is a natural product found in Coronilla scorpioides, Clausena dunniana, and other organisms with data available. Nodakenetin, isolated from Angelica decursiva, possesses antioxidant anti-inflammatory activities. Nodakenetin has the potential to be an antiarthritic and nerve tonic[1][2]. Nodakenetin, isolated from Angelica decursiva, possesses antioxidant anti-inflammatory activities. Nodakenetin has the potential to be an antiarthritic and nerve tonic[1][2]. S-(+)-Marmesin is a natural coumarin, exhibiting COX-2/5-LOX dual inhibitory activity. S-(+)-Marmesin is a natural coumarin, exhibiting COX-2/5-LOX dual inhibitory activity. S-(+)-Marmesin is a natural coumarin, exhibiting COX-2/5-LOX dual inhibitory activity.

   

Isopimpinellin

7H-Furo(3,2-g)(1)benzopyran-7-one, 4,9-dimethoxy- (8CI)(9CI)

C13H10O5 (246.052821)


Isopimpinellin is found in angelica. Isopimpinellin is present in the seeds of Pastinaca sativa (parsnip) Isopimpinellin belongs to the family of Furanocoumarins. These are polycyclic aromatic compounds containing a furan ring fused to a coumarin moeity. Isopimpinellin, an orally active compound isolated from Glomerella cingulata. Isopimpinellin blocks DNA adduct formation and skin tumor initiation by 7,12-dimethylbenz[a]anthracene. Isopimpinellin possesses anti-leishmania effect[1]. Isopimpinellin, an orally active compound isolated from Glomerella cingulata. Isopimpinellin blocks DNA adduct formation and skin tumor initiation by 7,12-dimethylbenz[a]anthracene. Isopimpinellin possesses anti-leishmania effect[1].

   

Byakangelicin

7H-Furo(3,2-g)(1)benzopyran-7-one, 9-(2,3-dihydroxy-3-methylbutoxy)-4-methoxy-, (R)-

C17H18O7 (334.10524780000003)


Byakangelicin is a member of psoralens. Byakangelicin is a natural product found in Murraya koenigii, Triphasia trifolia, and other organisms with data available. D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents > D011564 - Furocoumarins (Rac)-Byakangelicin is a racemate of Byakangelicin mainly isolated from the genus Angelica. Byakangelicin is an aldose-reductase inhibitor with an IC50 value of 6.2 μM[1]. (Rac)-Byakangelicin is a racemate of Byakangelicin mainly isolated from the genus Angelica. Byakangelicin is an aldose-reductase inhibitor with an IC50 value of 6.2 μM[1]. Byakangelicin, one of the active compounds found in the roots of Angelica gigas, can serve as a modulator to improve brain accumulation of diverse active compounds (Umb, Cur, and Dox) and enhance therapeutic effects[1]. Byakangelicin is likely to increase the expression of all PXR target genes (such as MDR1) and induce a wide range of agent-agent interactions. Byakangelicin can inhibit the effects of sex hormones, it may increase the catabolism of endogenous hormones[2]. Byakangelicin, one of the active compounds found in the roots of Angelica gigas, can serve as a modulator to improve brain accumulation of diverse active compounds (Umb, Cur, and Dox) and enhance therapeutic effects[1]. Byakangelicin is likely to increase the expression of all PXR target genes (such as MDR1) and induce a wide range of agent-agent interactions. Byakangelicin can inhibit the effects of sex hormones, it may increase the catabolism of endogenous hormones[2].

   

decursinol

(7S)-7-hydroxy-8,8-dimethyl-6,7-dihydropyrano[5,6-g]chromen-2-one

C14H14O4 (246.0892044)


D020536 - Enzyme Activators Decursinol, isolated from the roots of Angelica gigas, possesses antinociceptive effect with orally bioavailability. Decursinol possesses anti-tumor and anti-metastasis activity[1]. Decursinol, isolated from the roots of Angelica gigas, possesses antinociceptive effect with orally bioavailability. Decursinol possesses anti-tumor and anti-metastasis activity[1].

   

(2r)-9-methyl-2-[(2e)-6-methylhepta-2,5-dien-2-yl]-5-methylidenedec-8-en-1-yl acetate

(2r)-9-methyl-2-[(2e)-6-methylhepta-2,5-dien-2-yl]-5-methylidenedec-8-en-1-yl acetate

C22H36O2 (332.2715156)


   

heptadeca-2,8-dien-4,6-diyne-1,10-diol

heptadeca-2,8-dien-4,6-diyne-1,10-diol

C17H24O2 (260.17762039999997)


   

heptadeca-1,8,10-trien-4,6-diyn-3-ol

heptadeca-1,8,10-trien-4,6-diyn-3-ol

C17H22O (242.1670562)


   

heptadeca-7,9,15-trien-11,13-diyn-4-one

heptadeca-7,9,15-trien-11,13-diyn-4-one

C17H20O (240.151407)


   

3,7-dimethyl-2-{2-[2-(4-methylpent-3-en-1-yl)oxiran-2-yl]ethyl}octa-3,6-dien-1-yl acetate

3,7-dimethyl-2-{2-[2-(4-methylpent-3-en-1-yl)oxiran-2-yl]ethyl}octa-3,6-dien-1-yl acetate

C22H36O3 (348.26643060000004)


   

heptadeca-8,10-dien-4,6-diyn-1-yl acetate

heptadeca-8,10-dien-4,6-diyn-1-yl acetate

C19H26O2 (286.1932696)


   

heptadeca-2,8,10-trien-4,6-diyn-1-yl acetate

heptadeca-2,8,10-trien-4,6-diyn-1-yl acetate

C19H24O2 (284.17762039999997)


   

2-[2-(acetyloxy)propan-2-yl]-7-oxo-2h,3h-furo[3,2-g]chromen-3-yl 3-methylbut-2-enoate

2-[2-(acetyloxy)propan-2-yl]-7-oxo-2h,3h-furo[3,2-g]chromen-3-yl 3-methylbut-2-enoate

C21H22O7 (386.1365462)


   

(9z)-heptadeca-1,9-dien-4,6-diyne-3,8-dione

(9z)-heptadeca-1,9-dien-4,6-diyne-3,8-dione

C17H20O2 (256.146322)


   

2-{7-oxo-2h,3h-furo[3,2-g]chromen-2-yl}propyl 3-methylbut-2-enoate

2-{7-oxo-2h,3h-furo[3,2-g]chromen-2-yl}propyl 3-methylbut-2-enoate

C19H20O5 (328.13106700000003)


   

(3s,8e,10e)-heptadeca-1,8,10-trien-4,6-diyn-3-ol

(3s,8e,10e)-heptadeca-1,8,10-trien-4,6-diyn-3-ol

C17H22O (242.1670562)


   

8-hydroxyheptadeca-1,9-dien-4,6-diyn-3-one

8-hydroxyheptadeca-1,9-dien-4,6-diyn-3-one

C17H22O2 (258.1619712)


   

heptadeca-1,9-dien-4,6-diyne-3,8-dione

heptadeca-1,9-dien-4,6-diyne-3,8-dione

C17H20O2 (256.146322)


   

methyl 7-[(2-methylpropanoyl)oxy]-2-oxochromene-6-carboxylate

methyl 7-[(2-methylpropanoyl)oxy]-2-oxochromene-6-carboxylate

C15H14O6 (290.0790344)


   

(2s,3r)-2-[2-(acetyloxy)propan-2-yl]-7-oxo-2h,3h-furo[3,2-g]chromen-3-yl 2-methylpropanoate

(2s,3r)-2-[2-(acetyloxy)propan-2-yl]-7-oxo-2h,3h-furo[3,2-g]chromen-3-yl 2-methylpropanoate

C20H22O7 (374.1365462)


   

2-[2-(acetyloxy)propan-2-yl]-7-oxo-2h,3h-furo[3,2-g]chromen-3-yl 2-methylpropanoate

2-[2-(acetyloxy)propan-2-yl]-7-oxo-2h,3h-furo[3,2-g]chromen-3-yl 2-methylpropanoate

C20H22O7 (374.1365462)


   

2-[3-(acetyloxy)-7-oxo-2h,3h-furo[3,2-g]chromen-2-yl]propan-2-yl acetate

2-[3-(acetyloxy)-7-oxo-2h,3h-furo[3,2-g]chromen-2-yl]propan-2-yl acetate

C18H18O7 (346.10524780000003)


   

(8e,10r)-heptadec-8-en-4,6-diyne-1,10-diol

(8e,10r)-heptadec-8-en-4,6-diyne-1,10-diol

C17H26O2 (262.1932696)


   

3-(4-hydroxy-3-methoxyphenyl)prop-2-en-1-yl octadecanoate

3-(4-hydroxy-3-methoxyphenyl)prop-2-en-1-yl octadecanoate

C28H46O4 (446.3395916)


   

(2e,8e,10e)-heptadeca-2,8,10-trien-4,6-diyn-1-yl acetate

(2e,8e,10e)-heptadeca-2,8,10-trien-4,6-diyn-1-yl acetate

C19H24O2 (284.17762039999997)


   

(2r,3e)-3,7-dimethyl-2-{2-[(2s)-2-(4-methylpent-3-en-1-yl)oxiran-2-yl]ethyl}octa-3,6-dien-1-yl acetate

(2r,3e)-3,7-dimethyl-2-{2-[(2s)-2-(4-methylpent-3-en-1-yl)oxiran-2-yl]ethyl}octa-3,6-dien-1-yl acetate

C22H36O3 (348.26643060000004)


   

3-hydroxy-2-(propan-2-ylidene)-3h-furo[3,2-g]chromen-7-one

3-hydroxy-2-(propan-2-ylidene)-3h-furo[3,2-g]chromen-7-one

C14H12O4 (244.0735552)


   

(8e,10e)-heptadeca-8,10-dien-4,6-diyn-1-yl acetate

(8e,10e)-heptadeca-8,10-dien-4,6-diyn-1-yl acetate

C19H26O2 (286.1932696)


   

(2e,8e,10r)-heptadeca-2,8-dien-4,6-diyne-1,10-diol

(2e,8e,10r)-heptadeca-2,8-dien-4,6-diyne-1,10-diol

C17H24O2 (260.17762039999997)


   

(2s,3r)-2-[2-(acetyloxy)propan-2-yl]-7-oxo-2h,3h-furo[3,2-g]chromen-3-yl 3-methylbut-2-enoate

(2s,3r)-2-[2-(acetyloxy)propan-2-yl]-7-oxo-2h,3h-furo[3,2-g]chromen-3-yl 3-methylbut-2-enoate

C21H22O7 (386.1365462)


   

(2e,9z)-heptadeca-2,9-dien-4,6-diyn-1-ol

(2e,9z)-heptadeca-2,9-dien-4,6-diyn-1-ol

C17H24O (244.18270539999997)


   

6-hydroxy-7-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]chromen-2-one

6-hydroxy-7-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]chromen-2-one

C24H30O4 (382.214398)


   

(2s,3r)-3-hydroxy-2-(2-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}propan-2-yl)-2h,3h-furo[3,2-g]chromen-7-one

(2s,3r)-3-hydroxy-2-(2-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}propan-2-yl)-2h,3h-furo[3,2-g]chromen-7-one

C20H24O10 (424.13694039999996)


   

6-hydroxy-7-{[(2e,6e)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]oxy}chromen-2-one

6-hydroxy-7-{[(2e,6e)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]oxy}chromen-2-one

C24H30O4 (382.214398)


   

heptadec-8-en-4,6-diyne-1,10-diol

heptadec-8-en-4,6-diyne-1,10-diol

C17H26O2 (262.1932696)


   

(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-en-1-yl octadecanoate

(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-en-1-yl octadecanoate

C28H46O4 (446.3395916)


   

2-(2-methoxypropan-2-yl)furo[3,2-g]chromen-7-one

2-(2-methoxypropan-2-yl)furo[3,2-g]chromen-7-one

C15H14O4 (258.0892044)


   

(1s,2r,3s,6r)-6-(hydroxymethyl)-1,3-dimethyl-2-(3-methylbut-2-en-1-yl)-3-(4-methylpent-3-en-1-yl)cyclohexan-1-ol

(1s,2r,3s,6r)-6-(hydroxymethyl)-1,3-dimethyl-2-(3-methylbut-2-en-1-yl)-3-(4-methylpent-3-en-1-yl)cyclohexan-1-ol

C20H36O2 (308.2715156)


   

heptadeca-2,9-dien-4,6-diyn-1-ol

heptadeca-2,9-dien-4,6-diyn-1-ol

C17H24O (244.18270539999997)


   

2-{7-oxo-2h,3h-furo[3,2-g]chromen-2-yl}propan-2-yl 3-methylbut-2-enoate

2-{7-oxo-2h,3h-furo[3,2-g]chromen-2-yl}propan-2-yl 3-methylbut-2-enoate

C19H20O5 (328.13106700000003)


   

9-methyl-2-(6-methylhepta-2,5-dien-2-yl)-5-methylidenedec-8-en-1-yl acetate

9-methyl-2-(6-methylhepta-2,5-dien-2-yl)-5-methylidenedec-8-en-1-yl acetate

C22H36O2 (332.2715156)


   

2-[(2s)-7-oxo-2h,3h-furo[3,2-g]chromen-2-yl]propan-2-yl 3-methylbut-2-enoate

2-[(2s)-7-oxo-2h,3h-furo[3,2-g]chromen-2-yl]propan-2-yl 3-methylbut-2-enoate

C19H20O5 (328.13106700000003)


   

heptadeca-1,9-dien-4,6-diyn-3-one

heptadeca-1,9-dien-4,6-diyn-3-one

C17H22O (242.1670562)


   

2-[(2s,3r)-3-(acetyloxy)-7-oxo-2h,3h-furo[3,2-g]chromen-2-yl]propan-2-yl acetate

2-[(2s,3r)-3-(acetyloxy)-7-oxo-2h,3h-furo[3,2-g]chromen-2-yl]propan-2-yl acetate

C18H18O7 (346.10524780000003)


   

(8s,9z)-8-hydroxyheptadeca-1,9-dien-4,6-diyn-3-one

(8s,9z)-8-hydroxyheptadeca-1,9-dien-4,6-diyn-3-one

C17H22O2 (258.1619712)