NCBI Taxonomy: 3090219

Millettia conraui (ncbi_taxid: 3090219)

found 21 associated metabolites at species taxonomy rank level.

Ancestor: Millettia

Child Taxonomies: none taxonomy data.

Docosanol

InChI=1/C22H46O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23/h23H,2-22H2,1H

C22H46O (326.3548466)


Docosan-1-ol is a long-chain primary fatty alcohol that is docosane substituted by a hydroxy group at position 1. It has a role as an antiviral agent. It is a long-chain primary fatty alcohol and a fatty alcohol 22:0. It derives from a hydride of a docosane. Docosanol is a drug used for topical treatment for recurrent herpes simplex labialis episodes (episodes of cold sores or fever blisters). A saturated 22-carbon aliphatic alcohol, docosanol exhibits antiviral activity against many lipid enveloped viruses including herpes simplex virus (HSV). Docosanol inhibits fusion between the plasma membrane and the herpes simplex virus (HSV) envelope, thereby preventing viral entry into cells and subsequent viral replication. Docosanol is a natural product found in Populus tremula, Hypericum laricifolium, and other organisms with data available. Docosanol is a saturated 22-carbon aliphatic alcohol with antiviral activity. Docosanol has a distinct mechanism of action and inhibits fusion between the plasma membrane and the herpes simplex virus envelope, thereby preventing viral entry into cells and subsequent viral activity and replication. Docosanol is used topically in the treatment of recurrent herpes simplex labialis episodes and relieves associated pain and may help heal sores faster. Docosanol is a drug used for topical treatment for recurrent herpes simplex labialis episodes (episodes of cold sores or fever blisters). A saturated 22-carbon aliphatic alcohol, docosanol exhibits antiviral activity against many lipid enveloped viruses including herpes simplex virus (HSV). Docosanol inhibits fusion between the plasma membrane and the herpes simplex virus (HSV) envelope, thereby preventing viral entry into cells and subsequent viral replication. Docosanol is a saturated 22-carbon aliphatic alcohol which exhibits antiviral activity against many lipid enveloped viruses including herpes simplex virus (HSV). Docosanol speeds the healing of cold sores and fever blisters on the face or lips. It also relieves the accompanying symptoms, including tingling, pain, burning, and itching. Docosanol cannot, however, prevent cold sores or fever blisters from appearing. Docosan-1-ol is found in ginkgo nuts and potato. A long-chain primary fatty alcohol that is docosane substituted by a hydroxy group at position 1. It is a non-prescription medicine approved by the FDA to shorten healing time of cold sores. D - Dermatologicals > D06 - Antibiotics and chemotherapeutics for dermatological use > D06B - Chemotherapeutics for topical use > D06BB - Antivirals D000890 - Anti-Infective Agents > D000998 - Antiviral Agents C254 - Anti-Infective Agent > C281 - Antiviral Agent 1-Docosanol is a saturated fatty alcohol with reported inhibitory activity against lipid-enveloped viruses, including herpes simplex virus. 1-Docosanol is a saturated fatty alcohol with reported inhibitory activity against lipid-enveloped viruses, including herpes simplex virus.

   

beta-Amyrin

4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-icosahydropicen-3-ol

C30H50O (426.386145)


Beta-amryin, also known as B-amryin, is a member of the class of compounds known as triterpenoids. Triterpenoids are terpene molecules containing six isoprene units. Beta-amryin is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). Beta-amryin can be found in pigeon pea, which makes beta-amryin a potential biomarker for the consumption of this food product.

   

β-Amyrin

beta-amyrin-H2O

C30H50O (426.386145)


Beta-amyrin, also known as amyrin or (3beta)-olean-12-en-3-ol, is a member of the class of compounds known as triterpenoids. Triterpenoids are terpene molecules containing six isoprene units. Thus, beta-amyrin is considered to be an isoprenoid lipid molecule. Beta-amyrin is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). Beta-amyrin can be synthesized from oleanane. Beta-amyrin is also a parent compound for other transformation products, including but not limited to, erythrodiol, glycyrrhetaldehyde, and 24-hydroxy-beta-amyrin. Beta-amyrin can be found in a number of food items such as thistle, pepper (c. baccatum), wakame, and endive, which makes beta-amyrin a potential biomarker for the consumption of these food products. The amyrins are three closely related natural chemical compounds of the triterpene class. They are designated α-amyrin (ursane skeleton), β-amyrin (oleanane skeleton) and δ-amyrin. Each is a pentacyclic triterpenol with the chemical formula C30H50O. They are widely distributed in nature and have been isolated from a variety of plant sources such as epicuticular wax. In plant biosynthesis, α-amyrin is the precursor of ursolic acid and β-amyrin is the precursor of oleanolic acid. All three amyrins occur in the surface wax of tomato fruit. α-Amyrin is found in dandelion coffee . β-Amyrin, an ingredient of Celastrus hindsii, blocks amyloid β (Aβ)-induced long-term potentiation (LTP) impairment. β-amyrin is a promising candidate of treatment for AD[1]. β-Amyrin, an ingredient of Celastrus hindsii, blocks amyloid β (Aβ)-induced long-term potentiation (LTP) impairment. β-amyrin is a promising candidate of treatment for AD[1].

   

sitosterol

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

C29H50O (414.386145)


A member of the class of phytosterols that is stigmast-5-ene substituted by a beta-hydroxy group at position 3. C1907 - Drug, Natural Product > C28178 - Phytosterol > C68437 - Unsaturated Phytosterol D057847 - Lipid Regulating Agents > D000960 - Hypolipidemic Agents D009676 - Noxae > D000963 - Antimetabolites Beta-Sitosterol (purity>98\\%) is a plant sterol. Beta-Sitosterol (purity>98\\%) interfere with multiple cell signaling pathways, including cell cycle, apoptosis, proliferation, survival, invasion, angiogenesis, metastasis and inflammation[1]. Beta-Sitosterol (purity>98\%) is a plant sterol. Beta-Sitosterol (purity>98\%) interfere with multiple cell signaling pathways, including cell cycle, apoptosis, proliferation, survival, invasion, angiogenesis, metastasis and inflammation[1].

   

fujikinetin

3- (1,3-Benzodioxol-5-yl) -7-hydroxy-6-methoxy-4H-1-benzopyran-4-one

C17H12O6 (312.06338519999997)


   

5-Methoxydurmillone

5,6-Dimethoxy-3,4methylenedioxy-6",6"-dimethylpyrano [ 2",3":7,8 ] isoflavone

C23H20O7 (408.120897)


   

Durmillone

3- (1,3-Benzodioxol-5-yl) -6-methoxy-8,8-dimethyl-4H,8H-benzo [ 1,2-b:3,4-b ] dipyran-4-one

C22H18O6 (378.1103328)


   

Docosanol

1-Docosanol

C22H46O (326.3548466)


D - Dermatologicals > D06 - Antibiotics and chemotherapeutics for dermatological use > D06B - Chemotherapeutics for topical use > D06BB - Antivirals D000890 - Anti-Infective Agents > D000998 - Antiviral Agents C254 - Anti-Infective Agent > C281 - Antiviral Agent 1-Docosanol is a saturated fatty alcohol with reported inhibitory activity against lipid-enveloped viruses, including herpes simplex virus. 1-Docosanol is a saturated fatty alcohol with reported inhibitory activity against lipid-enveloped viruses, including herpes simplex virus.

   

3-(2h-1,3-benzodioxol-5-yl)-7-{[(2e)-3,7-dimethylocta-2,6-dien-1-yl]oxy}-6-methoxychromen-4-one

3-(2h-1,3-benzodioxol-5-yl)-7-{[(2e)-3,7-dimethylocta-2,6-dien-1-yl]oxy}-6-methoxychromen-4-one

C27H28O6 (448.1885788)


   

5,6-dimethoxy-3-(6-methoxy-2h-1,3-benzodioxol-5-yl)-8,8-dimethylpyrano[2,3-h]chromen-4-one

5,6-dimethoxy-3-(6-methoxy-2h-1,3-benzodioxol-5-yl)-8,8-dimethylpyrano[2,3-h]chromen-4-one

C24H22O8 (438.1314612)


   

3-(4-{[(2e)-3,7-dimethylocta-2,6-dien-1-yl]oxy}phenyl)-7-hydroxychromen-4-one

3-(4-{[(2e)-3,7-dimethylocta-2,6-dien-1-yl]oxy}phenyl)-7-hydroxychromen-4-one

C25H26O4 (390.18309960000005)


   

3-(2h-1,3-benzodioxol-5-yl)-7-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-6-methoxychromen-4-one

3-(2h-1,3-benzodioxol-5-yl)-7-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-6-methoxychromen-4-one

C27H28O6 (448.1885788)


   

3-(2h-1,3-benzodioxol-5-yl)-7-{[(2e,5e)-7-hydroxy-3,7-dimethylocta-2,5-dien-1-yl]oxy}-6-methoxychromen-4-one

3-(2h-1,3-benzodioxol-5-yl)-7-{[(2e,5e)-7-hydroxy-3,7-dimethylocta-2,5-dien-1-yl]oxy}-6-methoxychromen-4-one

C27H28O7 (464.1834938)


   

3-(2h-1,3-benzodioxol-5-yl)-7-[(7-hydroxy-3,7-dimethylocta-2,5-dien-1-yl)oxy]-6-methoxychromen-4-one

3-(2h-1,3-benzodioxol-5-yl)-7-[(7-hydroxy-3,7-dimethylocta-2,5-dien-1-yl)oxy]-6-methoxychromen-4-one

C27H28O7 (464.1834938)


   

2-{[1-(5-ethyl-6-methylheptan-2-yl)-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

2-{[1-(5-ethyl-6-methylheptan-2-yl)-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

C35H60O6 (576.4389659999999)


   

3-(4-{[(2e)-3,7-dimethylocta-2,6-dien-1-yl]oxy}phenyl)-7-hydroxy-5-methoxychromen-4-one

3-(4-{[(2e)-3,7-dimethylocta-2,6-dien-1-yl]oxy}phenyl)-7-hydroxy-5-methoxychromen-4-one

C26H28O5 (420.1936638)


   

stigmast-5-en-3-ol, (3β)-

stigmast-5-en-3-ol, (3β)-

C29H50O (414.386145)


   

5,6-dimethoxy-3-(4-methoxy-2h-1,3-benzodioxol-5-yl)-8,8-dimethylpyrano[2,3-h]chromen-4-one

5,6-dimethoxy-3-(4-methoxy-2h-1,3-benzodioxol-5-yl)-8,8-dimethylpyrano[2,3-h]chromen-4-one

C24H22O8 (438.1314612)


   

3-{4-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]phenyl}-7-hydroxy-5-methoxychromen-4-one

3-{4-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]phenyl}-7-hydroxy-5-methoxychromen-4-one

C26H28O5 (420.1936638)


   

3-{4-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]phenyl}-7-hydroxychromen-4-one

3-{4-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]phenyl}-7-hydroxychromen-4-one

C25H26O4 (390.18309960000005)